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Organosulfur-based polymers have unique properties that make them useful for targeted and managed drug delivery, which can improve therapy while reducing side effects. This work aims to provide a brief review of the synthesis strategies, characterization techniques, and packages of organosulfur-based polymers in drug delivery. More importantly, this work discusses the characterization, biocompatibility, controlled release, nanotechnology, and targeted therapeutic aspects of these important structural units. This review provides not only a good comprehension of organosulfur-based polymers but also an insightful discussion of potential future prospectives in research. The discovery of novel organosulfur polymers and innovations is highly expected to be stimulated in order to synthesize polymer prototypes with increased functional accuracy, efficiency, and low cost for many industrial applications. [ABSTRACT FROM AUTHOR]

We have developed a diversity‐oriented, substrate‐controlled, chemoselective synthetic method for a variety of structurally diverse 1‐sulfonylquinazoline‐2,4(1H,3H)‐diones and 2‐sulfonamidobenzonitriles. This substrate‐controlled synthesis is accomplished through the condensation reaction of 2‐(sulfonamido)benzamides with or without an N‐methyl group on the amides. The reactions are fulfilled within half an hour at room temperature with solid triphosgene as a convenient condensing agent and pyridine as an acid acceptor. This protocol features easily available starting materials, mild reaction conditions, easy experimental operation, and moderate to excellent yields of products. [ABSTRACT FROM AUTHOR]

In recent years, there has been a notable surge in the prominence of enantioenriched sulfur(VI) compounds within the chemical science, particularly in the realm of bioactive molecules. However, the synthesis of these enantioenriched sulfur(VI) compounds has posed significant challenges, necessitating the exploration of diverse synthetic methods. Accordingly, this review aims to provide an in‐depth analysis of the latest advancements in the synthesis of sulfoximines, sulfonimidate esters, sulfonimidamides, and sulfonimidoyl halides, with a focus on developments since 1971. [ABSTRACT FROM AUTHOR]

Background: Cervical cancer is an important global health problem. In this study we aimed to analyze trends in cervical cancer at the global, regional, and national levels from 1990 to 2019, to inform health service decision-making.Methods: Data on cervical cancer was extracted from the Global Burden of Disease study, 2019. Trends in cervical cancer burden were assessed based on estimated annual percentage change (EAPC) and age-standardized rate (ASR).Results: Globally, decreasing trends were observed in incidence, death, and disability adjusted life years (DALYs) of cervical cancer from 1990 to 2019, with respective EAPCs of - 0.38 (95% confidence interval [CI]: - 0.41 to - 0.34), - 0.93 (95%CI: - 0.98 to - 0.88), and - 0.95 (95 CI%: - 1.00 to - 0.90). Meanwhile, decreasing trends were detected in most sociodemographic index (SDI) areas and geographic regions, particularly death and DALYs in Central Latin America, with respective EAPCs of - 2.61 (95% CI: - 2.76 to - 2.46) and - 2.48 (95% CI: - 2.63 to - 2.32); hhowever, a pronounced increasing trend in incidence occurred in East Asia (EAPC = 1.33; 95% CI: 1.12 to 1.55). At the national level, decreasing trends in cervical cancer were observed in most countries/territories, particularly DALYs in the Maldives (EAPC = - 5.06; 95% CI: - 5.40 to - 4.72), Whereas increasing trends were detected in Lesotho, Zimbabwe, and Bulgaria.Conclusions: Slowly decreasing trends in cervical cancer were detected worldwide from 1990 to 2019. Cervical cancer remains a substantial health problem for women globally, requiring more effective prevention and control strategies. [ABSTRACT FROM AUTHOR]

Based on the Hard-Soft-Acid-Base theory, we developed and synthesized a unique crystalline adsorbent called MIL-101(Cr)-SMA-ED-PMG (SMA: styrene maleic anhydride; ED: ethylenediamine; PMG: N,N -di(phosphonomethyl)glycine). This adsorbent consists of polymer chains that are abundant in carboxyl and phosphate Lewis hard base groups. This was performed to enhance the efficient recuperation of electrophilic Lewis hard acid rare earth elements. The Neodymium(III) (Nd3+) and Europium(III) (Eu3+) ions reached adsorption equilibrium in the MIL-101(Cr)-SMA-ED-PMG material after 6 h at pH 5. The adsorption of Nd3+ and Eu3+ follows the pseudo-second-order kinetic and Langmuir models. The maximum adsorption capabilities were 102.7 mg/g for Nd3+ and 110.4 mg/g for Eu3+. In addition, when applying a concentration of 0.3 mol/L of HNO 3 or HCl, the adsorbent was nearly completely desorbed, and it remained stable for five cycles. The order of adsorption for the different REE ions was as follows: Eu3+ > Nd3+ > Ce3+ > La3+. The MIL-101(Cr)-SMA-ED-PMG compound demonstrated a remarkable 84 % selectivity in adsorbing Eu3+ compared to the other metal ions in the mixture (Na+, Mg2+, Co2+, Ni2+, and Zn2+). Furthermore, the adsorption of Eu3+ was not significantly influenced by changes in the aqueous conditions. The experiment conducted on a zinc ore simulated leachate exhibited the material remarkable capacity for Eu3+ separation and enrichment. MIL-101(Cr)-SMA-ED-PMG exhibits strong adsorption properties, exceptional selectivity, effective desorption, and significant potential for the recovery of rare earth elements (REEs). [Display omitted] • MIL-101(Cr)-SMA-ED-PMG is prepared by radical polymerization and post-synthetic modifications on MIL-101(Cr). • The adsorption capacity is 102.7 mg/g for Nd3+ and 110.4 mg/g for Eu3+. • The adsorbent exhibits 72.4-85.1% reusability and 84% selectivity for Eu3+. • The cation exchange and coordination are the main adsorption mechanisms. [ABSTRACT FROM AUTHOR]

The design and development of low-cost, abundant reserves, high catalytic activity and durability bifunctional electrocatalysts for water splitting are of great significance. Here, simple hydrothermal and hydrogen reduction methods were used to fabricate a uniform distribution of Fe-doped MoO 2 /MoO 3 sheets with abundant oxygen vacancies and heterojunctions on etched nickel foam (ENF). The Fe– MoO 2 /MoO 3 /ENF exhibited a small overpotential of 36 mV at 10 mA cm−2 for hydrogen evolution reaction (HER), an excellent oxygen evolution reaction (OER) overpotential of 310 mV at 100 mA cm−2 and outstanding stabilities of 95 h and 120 h for the HER and OER, respectively. As both cathode and anode catalysts, the heterogeneously structured Fe– MoO 2 /MoO 3 /ENF required a low cell voltage of 1.57 V at 10 mA cm−2. Density functional theory (DFT) calculations show that Fe doping and MoO 2 /MoO 3 heterojunctions can significantly reduce the band gap of the electrode, accelerate electron transport and reduce the potential barrier for water splitting. This work provides a new approach for designing metal ion doping and heterostructure formation that may be adapted to transition metal oxides for water splitting. Image 1 • Improve the adhesion of the materials by etching nickel foam (NF). • Two-step reaction simultaneously achieves iron doping and heterojunctions. • DFT calculations confirm that Fe doping increased the conductivity. • In situ grown heterojunctions greatly reduce the potential barrier. [ABSTRACT FROM AUTHOR]

The binding interaction of niraparib (MK-4827), a poly(ADP-ribose) polymerase inhibitor, with calf thymus deoxyribonucleic acid (ctDNA) has been explored by various theoretical and experimental techniques. Molecular docking models predicted that all the binding conformations of MK-4827 interaction with DNA are clustered into two types: one intercalates into the middle part of the DNA composed of A–T base pairs, and the other one binds with the bottom part of the DNA composed of C–G base pairs. Molecular dynamics simulations further concluded that MK-4827 could steadily intercalate the A–T base pairs of the DNA structure, and the hydrogen bonds and hydrophobic forces help maintain this combination. Fluorescence titration of MK-4827 by ctDNA indicated that the interaction involves static quenching, which resulted from the temperature dependence of the MK-4827–ctDNA complex and was further verified by fluorescence lifetime experiments. Iodide quenching, DNA melting, viscosity and fluorescence competitive experiments with two known intercalative binders confirmed that intercalation is the main DNA binding mode for MK-4827 and has certain influence on the conformation of the ctDNA as indicated by CD. [ABSTRACT FROM AUTHOR]

Highlights • Enantioseparation of sulfinamides on polysaccharide chiral stationary phases is reported. • All of 12 sulfinamides can be resolved with three columns, eleven for both OD-H and AD-H. • A valuable guide for chiral HPLC study or technology related to chiral sulfinyl compounds. Abstract Chiral sulfinamides are increasingly recognizedfor their extensive potential applications in chemistry, medicine and material science, yet chromatographic study on these compounds is seldom. In this article, we describe the enantioseparation of twelve closely related chiral sulfinamide derivatives on polysaccharide-based chiral stationary phases (CSPs). We investigated the factors affecting separation, such as the types of chiral columns, the concentration of polar alcohol and the column temperature. The acyclic sulfinamide derivatives—with the exception of a cyclic sulfinamide compound—were effectively resolved with a Chiralcel OD-H column and a mixture of n-hexane:isopropyl alcohol (90:10) as the mobile phase. All compounds except N-benzylidene-2-methylpropane-2-sulfinamide are baseline resolved on the Chiralpak AD-H column, but only eight compounds are resolved on a Chiralpak AS-H column under the given chromatographic conditions. This study offers valuable guidance for future chiral HPLC studies related to chiral sulfinamides. [ABSTRACT FROM AUTHOR]

Chiral organoselenium compounds have shown an important role as intermediates in many areas, such as drug discovery, organic catalysis, and nanomaterials. A lot of different methods have been developed to synthesize chiral compounds which contain selenium, because they have interesting properties and can be used in real life. Over the last few decades, a lot of progress has been made in synthesizing chiral organoselenium compounds. This work gives an overview of the progress made in creating new ways to synthesize chiral organoselenium compounds by categorizing them into groups based on the reactions they undergo. In addition, the use of chiral organoselenium compounds is also discussed. [ABSTRACT FROM AUTHOR]

Abstract: Most of compounds containing more than one reactive groups may produce several byproducts during the coupling process. Selective carbon‐heteroatom coupling reactions, which have merits of high synthetic efficiency and step economy, are the best choice to resolve the problem. Although they have made great progress, they deserve further exploration. This review discusses their recent advances and intend to inspire the research in the future. It is organized on the basis of selective carbon‐heteroatom coupling reaction types, including selective C−N and C−N, C−N and C−O, C−O and C−O, C−C and C−N coupling reactions. [ABSTRACT FROM AUTHOR]

[Display omitted] Allylic compounds are widely used in pharmaceutical, chemical and other industries, such as allyl indole derivatives widely present in alkaloids, allylylated derivatives of the antiviral drug acyclovir, and chiral allyl acinolides for the preparation of chiral amino acids. In recent years, vinylcyclopropanes has developed rapidly in organic synthetic chemistry. Activated vinylcyclopropanes are an important raw material for the synthesis of functionalized heterocyclic compounds or allyl derivatives. Transition metal-catalyzed allylation reaction of vinyl cyclopropanes can form new bonds with extensive nucleophiles containing C, N, O, Si, P and S centers. Progress on transition metal-catalyzed allylation of activated vinylcyclopropanes reviewed in this Digest Article. [ABSTRACT FROM AUTHOR]

Chiral sulfoximines have significant roles in pharmaceutical industry and agricultural chemicals. Furthermore, chiral structurally related sulfoximines are used for their wide potential applications in some uncharted territory. However, chromatographic study on these compounds has not been systematically performed. Herein, this paper describes the enantioseparation of 12 chiral sulfoximines on polysaccharide-based chiral stationary phases (CSPs). Separation factors of chiral column, high-performance liquid chromatography parameters such as mobile phase composition and column temperature were carefully investigated. Chiralcel OJ-H column can resolve all of the 12 compounds, while Chiralpak AD-H column and Chiralpak AS-H column can separate eight and nine molecules, respectively. The sulfoximines are effectively resolved with Chiralcel OJ-H column with a mixture of n -hexane/2-propanol (80:20) as the mobile phase. [ABSTRACT FROM AUTHOR]

An efficient cesium carbonate-mediated synthesis of phenothiazine derivatives from S-2-acetamidophenyl ethanethioates andortho-dihaloarenes has been developed. This protocol affords an efficient approach for the construction of phenothiazine derivatives without the need of transition-metal catalyst or ligand. A plausible mechanism is proposed. [ABSTRACT FROM PUBLISHER]

Samarium (Sm), as one of the lanthanide elements, has a broad application prospect in the synthesis of samarium cobalt permanent magnet materials with high temperature stability, corrosion resistance and oxidation resistance. Due to the unlimited demand of Sm(III), recycling of Sm(III) waste is an effective method to balance economy and supply. In this paper, three novel morpholine carboxylic acid ionic liquids (ILs) were rationally designed and successfully synthesized for the extraction of Sm(III). The effects of alkyl chain length of the ionic liquids, solution acidity, contact time, extractant concentration and temperature were tested in terms of the extraction performances. The results revealed that [(CH 2) 7 COOHmor][NTf 2 ] had the optimal extraction capacity, as well as the extraction efficiency of Sm increased with the increase of pH, reaching >99.9% when the pH was 1.8. In addition, the extraction equilibrium could be achieved within 1 min. Moreover, the slope analysis and FTIR spectral studies proposed a cation exchange extraction mechanism for Sm(III) by [(CH 2) 7 COOHmor][NTf 2 ]. The loaded Sm(III) in organic phase was easy to strip with 0.05 mol/L of HNO 3 , and the [(CH 2) 7 COOHmor][NTf 2 ] remained stable after 5 cycles. The research of transition metal extraction revealed that Sm(III) could be selectively separated from Ni(II) and Co(II) by adjusting the pH value of the solution. Finally, under the optimized extraction conditions, Sm 2 O 3 with 83.9% yield was obtained by the extraction-stripping-precipitation-calcination process, through the large-scale recovery applications of the simulated waste liquid. • The novel carboxyl-functionalized morpholine ionic liquids were designed and fabricated as novel extraction solvents. • The stripping ratios of Sm from ILs reached 99.9% via the back extraction. • The extraction performance of [(CH 2) 7 COOMor][Tf 2 N] maintained stable after 5 cycles. • Via adjusting the initial acidity of the aqueous phase, [(CH 2) 7 COOMor][Tf 2 N] could selectively separate Sm(III) from Co(II). [ABSTRACT FROM AUTHOR]

Sulfoxides and sulfinamides play important roles in the pharmaceutical industry, organic synthesis and fine chemicals. This review will demonstrate that, under catalysis by transition metals, β-sulfinyl esters, as nucleophilic reagents, react with a variety of electrophilic reagents to produce sulfoxides and sulfinamides. The important prospect of the asymmetric catalytic synthesis of chiral sulfur-containing molecules in this field is described. [ABSTRACT FROM AUTHOR]

A white light/iodosuccinimide (NIS)‐promoted three component reaction of alkenes, N‐sulfonylhydrazones, and diorganyl diselenides for synthesis of organylselenylethyl sulfonylhydrazones under air is disclosed. This intermolecular aminoselenylation of alkenes using N‐tosylhydrazones as nitrogen source was performed under mild conditions and well tolerated for common groups. In addition, heteroaryl and aliphatic diselenides also gave the target compounds. Gram‐scale reaction also carried out smoothly. This protocol has a wide range of substrates and affords moderate to high yields and excellent regioselectivities. The photoactive intermediates from the interaction between NIS and diphenyl diselenide was detected by UV‐visible absorption spectra, which matches the wavelength of the applied white LED. A reasonable mechanism was proposed based on UV‐visible light experiments and control experiments. [ABSTRACT FROM AUTHOR]

Sulfoximines, a ubiquitous class of structural motifs, are widely present in bioactive molecules and functional materials that have received considerable attention from modern organic chemistry, pharmaceutical industries, and materials science. Sulfoximines have proved to be an effective directing group for C–H functionalization which was widely investigated for the synthesis of cyclic sulfoximines. Within the last decade, great progress has been achieved in the synthesis of cyclic sulfoximines. Thus, this review highlights the recent advances in the synthesis of cyclic sulfoximines via the C–H activation strategy and is classified based on the substrate types. [ABSTRACT FROM AUTHOR]

Abstract: Sulfoxides are extensively used in chemical and pharmaceutical industries. Various catalytically synthetic methods were reported, but in common 1–10(mol)% catalyst loading were demanded. Sulfide oxidation catalyzed by vanadyl complexes of N-salicylidene α-amino acids with catalyst loading as low as 0.03(mol)% gave high yields at room temperature with aqueous hydrogen peroxide as an oxidant, which is a green, solvent-free, energy-saving and easy-operated protocol. In contrast, vanadyl complexes of N-salicylidene amino alcohols could not, even at 0.1(mol)%. The possible reason is that the stronger acidity of N-salicylidene α-amino acids makes their vanadyl complexes stable to aqueous hydrogen peroxide. This rule may be used in designing other high efficient catalysts, especially with aqueous hydrogen peroxide as an oxidant. [Copyright &y& Elsevier]

The axially chiral monophosphine 2-(diphenylphosphino)-2'-methoxy-1,1'-binaphthyl (MeO-MOP) is a versatile ligand. We report a shorter (four steps from chiral BINOL), more atom-economical synthetic route to MeO-MOP. (R)-BINOL is transformed into its monomethyl ether by the Mitsunobu reaction, and the latter is reacted with triflic anhydride to give its triflate. The C-P coupling of the triflate and diphenylphosphine oxide catalyzed by palladium give a phosphine oxide, the precursor of (R)-MeO-MOP, which is reduced with trichlorosilane to furnish (R)-MeO-MOP. [image omitted] [ABSTRACT FROM AUTHOR]

Abstract: The enantioselective oxidation of allyl sulfides with a vanadyl complex of 3,5-diiodosalicylidene tert-leucinol as a catalyst and aqueous hydrogen peroxide as an oxidant afforded chiral allyl sulfoxides with high enantioselectivities of up to 97.3% ee and moderate yields. [Copyright &y& Elsevier]

Mild and efficient procedures have been developed for synthesis of 1,8-naphthalide and 1,8-naphthalenedimethanol. In an ice-water bath, 1,8-naphthalide was prepared from 1,8-naphthlic anhydride using LiAlH4 as reducing agent. 1,8-Naphthalenedimethanol was obtained with good yield from reduction of 1,8-naphthalic anhydride by LiAlH4 and Lewis acids at room temperature. The effects of various factors on the reduction of 1,8-naphthalic anhydride with LiAlH4 were investigated. [ABSTRACT FROM AUTHOR]

H8-MonoPhos, a new stable and readily soluble monodentate phosphoramidite ligand, has been facilely prepared from H8-BINOL. The ligand achieved up to 99.9% ee and 96.7% ee in hydrogenation of dehydroalanine and dehydrohomophenylalanine in a S/C ratio of 500:1, respectively, which are among the best results to date. For dehydrophenylalanine derivatives, it gave good to excellent enantioselectivity. Some factors controlling the enantioselectivity and conversion were examined and are discussed. The interesting effects of ligand/rhodium ratio on the enantioselectivity and conversion were observed, which a mechanism was proposed to explain. [Copyright &y& Elsevier]

N‐Sulfenylation of sulfoximines with thiosulfonates under mild conditions was disclosed. By our method, a series of aliphatic and aromatic N‐sulfenyl sulfoximines were synthesized with good to excellent yields in the absence of transition metals. The applicability of this method was demonstrated by gram scale experiments. [ABSTRACT FROM AUTHOR]

In-vitro assessment of the binding properties of MK-0457, a novel Aurora kinase inhibitor, with human serum albumin: computer simulations in combination with multi-spectroscopic, esterase activity and microscopic studies. • MK-0457 bound to site 2 via vander Waals and hydrogen bonds. • Multispectroscopic comfirmed the binding was initiated by static quenching type. • MK-0457 could perturb the helicity of HSA and induce its conformational changes. • The esterase activity of HSA was decreased upon MK-0457 binding. • The morphology of HSA changed induced by interactions with MK-0457. MK-0457, a new pan-aurora kinase inhibitor, is in Phase II clinical development for the treatment of multiple tumor types and hematologic malignancies. The present work explored the dynamic behaviors and interaction mechanism of MK-0457 to human serum albumin (HSA) and the effect on the esterase-like activity and conformation of HSA by computer simulations and experiments. Docking and molecular dynamics trajectory analysis indicated that MK-0457 stably bound to Sudlow's site 2 of HSA by multiple types of interaction forces. Competitive experiments further verified MK-0457 was bound at first to Sudlow's site 2 and then the excess of drug was bound to Sudlow's site 1. The steady-state fluorescence combined with ultraviolet–visible absorption and fluorescence lifetime measurements specified a static quenching mechanism with association constants of 104 M−1 reflecting moderate binding affinity of MK-0457 for HSA. The analysis of R g values showed that the structure of HSA became loose due to MK-0457 binding, inducing slight conformational changes of HSA, which was consistent with the results obtained from circular dichroism, synchronous, and 3D fluorescence spectroscopy. The esterase-like activity of HSA showed that MK-0457 inhibits the catalytic activity of subdomain IIIA of HSA by binding to the vital residues TYR411. Atomic force microscopy images indicated that MK-0457 affects the molecular sizes of HSA by transforming the morphology of HSA from aggregation diploids to small monomers. This study is beneficial for understanding the biological action of MK-0457, providing additional information about the feasibility of its transport and accumulation in blood plasma. [ABSTRACT FROM AUTHOR]

H8-MonoPhos, a new stable and easily prepared monodentate phosphoramidite ligand, has been synthesized from H8-BINOL. The ligand showed extremely highly enantioselectivity of higher than 99.9% e.e. in the asymmetric Rh-catalyzed hydrogenation of α-dehydroamino acids. Our study further supports the new concept that there is no gap in efficiency and enantioselectivity between monodentate and chelating ligands for asymmetric catalysis. [Copyright &y& Elsevier]

Objective: To compare the outcomes of totally percutaneous in situ microneedle puncture for left subclavian artery (LSA) fenestration (ISMF) and chimney technique in type B aortic dissection (TBAD) during thoracic endovascular aortic repair (TEVAR).Data on patients who underwent either chimney–TEVAR (n = 89) or ISMF–TEVAR (n = 113) from October 2018 to April 2022 were analyzed retrospectively. The primary outcomes were mortality and major complications at 30 days and during follow-up.The technical success rate was 84.3% in the chimney group and 93.8% in the ISMF group (p = 0.027). The incidence of immediate endoleakage was significantly higher in the chimney than ISMF group (15.7% vs 6.2%, respectively; p = 0.027). The 1- and 3-year survival rates in the chimney and ISMF groups were 98.9% ± 1.1% vs 98.1% ± 0.9% and 86.5% ± 6.3% vs 92.6% ± 4.1%, respectively (log-rank p = 0.715). The 3-year rate of cumulative freedom from branch occlusion in the chimney and ISMF group was 95.4% ± 2.3% vs 100%, respectively (log-rank p = 0.023).Both ISMF–TEVAR and chimney–TEVAR achieved satisfactory short- and mid-term outcomes for the preservation of the LSA in patients with TBAD. ISMF–TEVAR appears to offer better clinical outcomes with higher patency and lower reintervention rates. However, ISMF–TEVAR had longer operation times with higher procedure expenses.When LSA revascularization is required during TEVAR, in situ, fenestration, and chimney techniques are all safe and effective methods; in situ, fenestration-TEVAR appears to offer better clinical outcomes, but takes longer and is more complicated.LSA revascularization during TEVAR reduces post-operative complication rates.Both in situ ISMF–TEVAR and chimney–TEVAR are safe and effective techniques for the preservation of the LSA during TEVAR.The chimney technique is associated with a higher incidence of endoleakage and branch occlusion, but ISMF–TEVAR is a more complicated and expensive technique.LSA revascularization during TEVAR reduces post-operative complication rates.Both in situ ISMF–TEVAR and chimney–TEVAR are safe and effective techniques for the preservation of the LSA during TEVAR.The chimney technique is associated with a higher incidence of endoleakage and branch occlusion, but ISMF–TEVAR is a more complicated and expensive technique.Materials and methods: To compare the outcomes of totally percutaneous in situ microneedle puncture for left subclavian artery (LSA) fenestration (ISMF) and chimney technique in type B aortic dissection (TBAD) during thoracic endovascular aortic repair (TEVAR).Data on patients who underwent either chimney–TEVAR (n = 89) or ISMF–TEVAR (n = 113) from October 2018 to April 2022 were analyzed retrospectively. The primary outcomes were mortality and major complications at 30 days and during follow-up.The technical success rate was 84.3% in the chimney group and 93.8% in the ISMF group (p = 0.027). The incidence of immediate endoleakage was significantly higher in the chimney than ISMF group (15.7% vs 6.2%, respectively; p = 0.027). The 1- and 3-year survival rates in the chimney and ISMF groups were 98.9% ± 1.1% vs 98.1% ± 0.9% and 86.5% ± 6.3% vs 92.6% ± 4.1%, respectively (log-rank p = 0.715). The 3-year rate of cumulative freedom from branch occlusion in the chimney and ISMF group was 95.4% ± 2.3% vs 100%, respectively (log-rank p = 0.023).Both ISMF–TEVAR and chimney–TEVAR achieved satisfactory short- and mid-term outcomes for the preservation of the LSA in patients with TBAD. ISMF–TEVAR appears to offer better clinical outcomes with higher patency and lower reintervention rates. However, ISMF–TEVAR had longer operation times with higher procedure expenses.When LSA revascularization is required during TEVAR, in situ, fenestration, and chimney techniques are all safe and effective methods; in situ, fenestration-TEVAR appears to offer better clinical outcomes, but takes longer and is more complicated.LSA revascularization during TEVAR reduces post-operative complication rates.Both in situ ISMF–TEVAR and chimney–TEVAR are safe and effective techniques for the preservation of the LSA during TEVAR.The chimney technique is associated with a higher incidence of endoleakage and branch occlusion, but ISMF–TEVAR is a more complicated and expensive technique.LSA revascularization during TEVAR reduces post-operative complication rates.Both in situ ISMF–TEVAR and chimney–TEVAR are safe and effective techniques for the preservation of the LSA during TEVAR.The chimney technique is associated with a higher incidence of endoleakage and branch occlusion, but ISMF–TEVAR is a more complicated and expensive technique.Results: To compare the outcomes of totally percutaneous in situ microneedle puncture for left subclavian artery (LSA) fenestration (ISMF) and chimney technique in type B aortic dissection (TBAD) during thoracic endovascular aortic repair (TEVAR).Data on patients who underwent either chimney–TEVAR (n = 89) or ISMF–TEVAR (n = 113) from October 2018 to April 2022 were analyzed retrospectively. The primary outcomes were mortality and major complications at 30 days and during follow-up.The technical success rate was 84.3% in the chimney group and 93.8% in the ISMF group (p = 0.027). The incidence of immediate endoleakage was significantly higher in the chimney than ISMF group (15.7% vs 6.2%, respectively; p = 0.027). The 1- and 3-year survival rates in the chimney and ISMF groups were 98.9% ± 1.1% vs 98.1% ± 0.9% and 86.5% ± 6.3% vs 92.6% ± 4.1%, respectively (log-rank p = 0.715). The 3-year rate of cumulative freedom from branch occlusion in the chimney and ISMF group was 95.4% ± 2.3% vs 100%, respectively (log-rank p = 0.023).Both ISMF–TEVAR and chimney–TEVAR achieved satisfactory short- and mid-term outcomes for the preservation of the LSA in patients with TBAD. ISMF–TEVAR appears to offer better clinical outcomes with higher patency and lower reintervention rates. However, ISMF–TEVAR had longer operation times with higher procedure expenses.When LSA revascularization is required during TEVAR, in situ, fenestration, and chimney techniques are all safe and effective methods; in situ, fenestration-TEVAR appears to offer better clinical outcomes, but takes longer and is more complicated.LSA revascularization during TEVAR reduces post-operative complication rates.Both in situ ISMF–TEVAR and chimney–TEVAR are safe and effective techniques for the preservation of the LSA during TEVAR.The chimney technique is associated with a higher incidence of endoleakage and branch occlusion, but ISMF–TEVAR is a more complicated and expensive technique.LSA revascularization during TEVAR reduces post-operative complication rates.Both in situ ISMF–TEVAR and chimney–TEVAR are safe and effective techniques for the preservation of the LSA during TEVAR.The chimney technique is associated with a higher incidence of endoleakage and branch occlusion, but ISMF–TEVAR is a more complicated and expensive technique.Conclusion: To compare the outcomes of totally percutaneous in situ microneedle puncture for left subclavian artery (LSA) fenestration (ISMF) and chimney technique in type B aortic dissection (TBAD) during thoracic endovascular aortic repair (TEVAR).Data on patients who underwent either chimney–TEVAR (n = 89) or ISMF–TEVAR (n = 113) from October 2018 to April 2022 were analyzed retrospectively. The primary outcomes were mortality and major complications at 30 days and during follow-up.The technical success rate was 84.3% in the chimney group and 93.8% in the ISMF group (p = 0.027). The incidence of immediate endoleakage was significantly higher in the chimney than ISMF group (15.7% vs 6.2%, respectively; p = 0.027). The 1- and 3-year survival rates in the chimney and ISMF groups were 98.9% ± 1.1% vs 98.1% ± 0.9% and 86.5% ± 6.3% vs 92.6% ± 4.1%, respectively (log-rank p = 0.715). The 3-year rate of cumulative freedom from branch occlusion in the chimney and ISMF group was 95.4% ± 2.3% vs 100%, respectively (log-rank p = 0.023).Both ISMF–TEVAR and chimney–TEVAR achieved satisfactory short- and mid-term outcomes for the preservation of the LSA in patients with TBAD. ISMF–TEVAR appears to offer better clinical outcomes with higher patency and lower reintervention rates. However, ISMF–TEVAR had longer operation times with higher procedure expenses.When LSA revascularization is required during TEVAR, in situ, fenestration, and chimney techniques are all safe and effective methods; in situ, fenestration-TEVAR appears to offer better clinical outcomes, but takes longer and is more complicated.LSA revascularization during TEVAR reduces post-operative complication rates.Both in situ ISMF–TEVAR and chimney–TEVAR are safe and effective techniques for the preservation of the LSA during TEVAR.The chimney technique is associated with a higher incidence of endoleakage and branch occlusion, but ISMF–TEVAR is a more complicated and expensive technique.LSA revascularization during TEVAR reduces post-operative complication rates.Both in situ ISMF–TEVAR and chimney–TEVAR are safe and effective techniques for the preservation of the LSA during TEVAR.The chimney technique is associated with a higher incidence of endoleakage and branch occlusion, but ISMF–TEVAR is a more complicated and expensive technique.Clinical relevance statement: To compare the outcomes of totally percutaneous in situ microneedle puncture for left subclavian artery (LSA) fenestration (ISMF) and chimney technique in type B aortic dissection (TBAD) during thoracic endovascular aortic repair (TEVAR).Data on patients who underwent either chimney–TEVAR (n = 89) or ISMF–TEVAR (n = 113) from October 2018 to April 2022 were analyzed retrospectively. The primary outcomes were mortality and major complications at 30 days and during follow-up.The technical success rate was 84.3% in the chimney group and 93.8% in the ISMF group (p = 0.027). The incidence of immediate endoleakage was significantly higher in the chimney than ISMF group (15.7% vs 6.2%, respectively; p = 0.027). The 1- and 3-year survival rates in the chimney and ISMF groups were 98.9% ± 1.1% vs 98.1% ± 0.9% and 86.5% ± 6.3% vs 92.6% ± 4.1%, respectively (log-rank p = 0.715). The 3-year rate of cumulative freedom from branch occlusion in the chimney and ISMF group was 95.4% ± 2.3% vs 100%, respectively (log-rank p = 0.023).Both ISMF–TEVAR and chimney–TEVAR achieved satisfactory short- and mid-term outcomes for the preservation of the LSA in patients with TBAD. ISMF–TEVAR appears to offer better clinical outcomes with higher patency and lower reintervention rates. However, ISMF–TEVAR had longer operation times with higher procedure expenses.When LSA revascularization is required during TEVAR, in situ, fenestration, and chimney techniques are all safe and effective methods; in situ, fenestration-TEVAR appears to offer better clinical outcomes, but takes longer and is more complicated.LSA revascularization during TEVAR reduces post-operative complication rates.Both in situ ISMF–TEVAR and chimney–TEVAR are safe and effective techniques for the preservation of the LSA during TEVAR.The chimney technique is associated with a higher incidence of endoleakage and branch occlusion, but ISMF–TEVAR is a more complicated and expensive technique.LSA revascularization during TEVAR reduces post-operative complication rates.Both in situ ISMF–TEVAR and chimney–TEVAR are safe and effective techniques for the preservation of the LSA during TEVAR.The chimney technique is associated with a higher incidence of endoleakage and branch occlusion, but ISMF–TEVAR is a more complicated and expensive technique.Key Points: To compare the outcomes of totally percutaneous in situ microneedle puncture for left subclavian artery (LSA) fenestration (ISMF) and chimney technique in type B aortic dissection (TBAD) during thoracic endovascular aortic repair (TEVAR).Data on patients who underwent either chimney–TEVAR (n = 89) or ISMF–TEVAR (n = 113) from October 2018 to April 2022 were analyzed retrospectively. The primary outcomes were mortality and major complications at 30 days and during follow-up.The technical success rate was 84.3% in the chimney group and 93.8% in the ISMF group (p = 0.027). The incidence of immediate endoleakage was significantly higher in the chimney than ISMF group (15.7% vs 6.2%, respectively; p = 0.027). The 1- and 3-year survival rates in the chimney and ISMF groups were 98.9% ± 1.1% vs 98.1% ± 0.9% and 86.5% ± 6.3% vs 92.6% ± 4.1%, respectively (log-rank p = 0.715). The 3-year rate of cumulative freedom from branch occlusion in the chimney and ISMF group was 95.4% ± 2.3% vs 100%, respectively (log-rank p = 0.023).Both ISMF–TEVAR and chimney–TEVAR achieved satisfactory short- and mid-term outcomes for the preservation of the LSA in patients with TBAD. ISMF–TEVAR appears to offer better clinical outcomes with higher patency and lower reintervention rates. However, ISMF–TEVAR had longer operation times with higher procedure expenses.When LSA revascularization is required during TEVAR, in situ, fenestration, and chimney techniques are all safe and effective methods; in situ, fenestration-TEVAR appears to offer better clinical outcomes, but takes longer and is more complicated.LSA revascularization during TEVAR reduces post-operative complication rates.Both in situ ISMF–TEVAR and chimney–TEVAR are safe and effective techniques for the preservation of the LSA during TEVAR.The chimney technique is associated with a higher incidence of endoleakage and branch occlusion, but ISMF–TEVAR is a more complicated and expensive technique.LSA revascularization during TEVAR reduces post-operative complication rates.Both in situ ISMF–TEVAR and chimney–TEVAR are safe and effective techniques for the preservation of the LSA during TEVAR.The chimney technique is associated with a higher incidence of endoleakage and branch occlusion, but ISMF–TEVAR is a more complicated and expensive technique. [ABSTRACT FROM AUTHOR]

Abstract: Substituted dibenzyl diselenides are synthesized in good yields (74–91 %) by SN2 nucleophilic substitution of benzylic trimethylammonium salts and diselenide dianion (Se2−), in situ generated from elemental selenium, under basic conditions. Highly enantiopure dibenzylic diselenides (95–98 % ee) with reverse configurations to their enantioenriched quaternary ammonium salts are obtained, if benzylic quaternary ammonium salts, synthesized from enantiomerically enriched amines, are used. [ABSTRACT FROM AUTHOR]

A three‐component reaction involving alkenes, N‐sulfonylhydrazones, and N‐bromosuccinimide (NBS) is described that uses Indium(III) triflate for the synthesis of bromoethyl sulfonyl hydrazones. Using N‐tosylhydrazones as a nitrogen source and NBS as a bromine source, this intermolecular aminobromination of alkenes is carried out under air in mild conditions. A mechanism of electrophilic addition is proposed based on the GC‐MS analytical result. [ABSTRACT FROM AUTHOR]

Organochalcogen molecules have extensive applications in various fields. They serve as pharmaceuticals, ligands, organocatalysts, agrochemicals, and other functional materials. Difunctionalization of olefins, which belong to a class of multicomponent reactions, is a successful technique for introducing two functional moieties in a single‐step reaction, both in terms of atom economy and step economy. The difunctionalization of olefins with diorganyl dichalcogenides may effectively increase the molecular complexity, which has achieved significant advancements in recent decades. This article describes recent advancements in the difunctionalization of olefins with diorganyl diselenides and diorganyl disulfides. [ABSTRACT FROM AUTHOR]

Chiral thioethers is an important class of organosulfur molecules with extensive applications, especially in the field of medicine and organic synthesis. This review discusses the recent progress of synthesis of enantioenriched chiral thioethers and hopes to be helpful for related research in the future. It is summarized from organosulfur compounds‐participating organic reaction types, including nucleophilic substitution, cross coupling, sulfa‐Michael addition, sulfenylation, asymmetric allylic reaction, asymmetric Doyle‐Kirmse reaction, Pummerer‐type rearrangement, Smiles rearrangement,[2,3] Stevens and Sommelet‐Hauser rearrangement. [ABSTRACT FROM AUTHOR]

Enantiomerically enriched five‐ and six‐membered benzo oxygen heterocycles are privileged architectures in functional organic molecules. Over the last several years, many effective methods have been established to access these compounds. However, comprehensive documents cover updated methodologies still in highly demand. In this review, recent transition metal catalyzed transformations lead to chiral five‐ and six‐membered benzo oxygen heterocycles are presented. The mechanism and chirality transfer or control processes are also discussed in details. [ABSTRACT FROM AUTHOR]

A three‐component reaction of olefins, indoles, and diaryl diselenides catalyzed by copper chloride under irradiation of blue LED light is disclosed. Various diaryl diselenides including diheteroaryl diselenides are suitable for this bifunctionalization of olefins. This protocol provides 26 examples of β‐(hetero)arylselenyl indoles in 60%–87% yields. The proposed mechanism involves activation of diaryl diselenides by coordination with copper chloride, generation of arylselenium cations by heterolysis of activated diaryl diselenides, electrophilic addition of arylselenium cations to styrenes, and then Friedel–Crafts‐type alkylation at the 3‐position of NH‐indoles. [ABSTRACT FROM AUTHOR]

A C 2 -symmetric, chiral bis-cyclosulfinamide-olefin ligand composed of two 1-oxo-2,3-dihydro-1,2-benzisothiazole moieties with rigid skeletons and a conformationally flexible butenylene chain is disclosed for the first time. HRMS and 1 H NMR analyses verify that the in situ-generated complex of the ligand and [Rh(C 2 H 4 ) 2 Cl] 2 possesses a rhodium (I) center coordinated to the tridentate ligand via two sulfinyl moieties and a CdbndC bond. The chiral ligand provided extremely high enantioselectivity (up to >99%ee) in the Rh-catalyzed asymmetric 1,4-additions of arylboronic acids to cyclohexenone and cyclopentenone. The tridentate ligand gave much higher enantioselectivity than the analogous chiral bidentate ligands. [ABSTRACT FROM AUTHOR]

Pedunculated hepatocellular carcinoma (P‑HCC) is a rare type of HCC, defined as a carcinoma protruding from the liver with or without a pedicle with a low degree of liver invasion. The present study aimed to evaluate the characteristics of blood supply of P‑HCC prior to and following transcatheter arterial chemoembolization (TACE) treatment. Angiographic findings prior to and following TACE treatment in 39 patients with P‑HCC were analyzed retrospectively. Angiography performed at the first TACE session revealed 70 tumor‑feeding arteries collectively in all patients, including 31/70 (44.0%) extrahepatic parasitic arteries in 23/39 patients (59.0%). The intrahepatic arteries served as the main blood supply to P‑HCC in all patients. Extrahepatic collateral blood supplies to P‑HCCs were significantly associated with larger tumor diameter (χ2=164.000, P<0.001), but not tumor location (χ2=7.358, P=0.061). Following repeated TACE treatment, all angiographies revealed a total of 131 tumor feeding arteries collectively in all patients, including intrahepatic arteries (54/131) and extrahepatic collateral arteries (78/131) in 31 patients (79.5%). Compared with angiographies performed at the initial TACE treatment, these results also demonstrated an increase in the number of extrahepatic collateral arteries, which produced 47 new blood vessels (χ2=4.278, P=0.039). P‑HCC tumor lesions readily acquired a parasitic blood supply from adjacent vessels following repeated TACE. Intrahepatic arteries functioned as the main blood supply for P‑HCC, whereas extrahepatic collateral arteries were complementary to P‑HCC, regardless of whether the patient was pre‑ or post‑TACE. Extrahepatic collateral supplies to P‑HCCs that originated from adjacent vessels were rich, were closely associated with tumor size, and were prone to be newly established following repeated TACE. [ABSTRACT FROM AUTHOR]

N-Aryl-α-amino amides including their chiral isomers have demonstrated important applications as pharmaceutical drugs; however, to date, a one-step synthetic route for them still remains to be developed. Herein, an efficient ligand-free copper-catalyzed selective C–N coupling reaction of diaryliodonium salts and dinucleophiles under mild conditions was realized. Diaryliodonium salts prefer to react with dinucleophiles at the site of stronger alkalic amino groups. Thus, a general aliphatic amino-selective N-arylation of α-amino amides was disclosed. Additionally, copper-catalyzed N-arylation of diaryliodonium salts afforded the same products as obtained via palladium-catalyzed reactions of aryl halides. [ABSTRACT FROM AUTHOR]

Ring‐opening addition reaction of activated vinyl cyclopropanes with N‐tosylhydrazones in the presence of palladium(0) and triphenylphosphine affords N‐tosylhydrazone butenylmalonate compounds. Aromatic aldehyde‐derived N‐tosylhydrazones produced terminal and internal N‐allylated products, in which the terminal products are the main. While ketone‐derived tosylhydrazones produced only terminal addition products. The transformation relationship of the terminal and internal N‐allylated products in the reaction was also observed. A reasonable mechanism is proposed based on preliminary experimental results. [ABSTRACT FROM AUTHOR]

1,1-Difunctionalization of α ‑carbonyl sulfur ylides and thiosulfonates under simple conditions is disclosed. In this protocol, two new C–S bonds are constructed in a one-step reaction. A series of aliphatic and aromatic β -keto thiosulfones were obtained in moderate to good yields. This reaction probably proceeds through sulfur ylide-involved- nucleophilic substitution of an ion pair within a solvent cage. [ABSTRACT FROM AUTHOR]

[Display omitted] A facile Brønsted acid-promoted three-component reaction of 2-methoxythiophene, sulfinates and water at room temperature has been discovered. Under the mild conditions, a series of γ- mercapto -β- sulfonyl esters were obtained in moderate to good yields. The control experiments support the reaction mechanism involves in three processes: 1,5-H shift, Michael addition and ring opening in water. [ABSTRACT FROM AUTHOR]

The article discusses the recognition of chiral sulfinamides including t-butanesulfinamide and p-toluenesulfinamide as versatile reagents that have extensive applications in the synthesis of natural products. It cites the typical procedure of N-monoalkylation of chiral sulfinamides and the general procedure for the dialkylation of chiral sulfinamides. It also cites the purification of the crude product using silica gel column chromatography.

In recent years, sulfenate anions as key intermediates in enantioselective synthesis have attracted considerable attention. Typically, development of novel synthetic methods to generate sulfenate anions allows for the preparation of various enantiopure sulfoxides, which are prevalently used as auxiliaries, ligands, organocatalysts, and biologically active compounds. This review presents the in situ preparation methods and the recent applications of sulfenate anions in catalytic asymmetric synthesis of chiral sulfoxides. [ABSTRACT FROM AUTHOR]

Abstract: A catalyst based on a new biarylphosphine ligand (3) for the Pd-catalyzed cross-coupling reactions of amides and aryl chlorides is described. This system shows the highest turnover frequencies reported to date for these reactions, especially for aryl chloride substrates bearing an ortho substituent. An array of amides and aryl chlorides were successfully reacted in good to excellent yields. [Copyright &y& Elsevier]

Highly efficient adsorbents, which can effectively remove both metal ions and dyes from wastewater with robust stability, are strongly required for the remediation of current polluted aqueous system, but still a challenge to be realized. Herein, a new adsorbent has been designed to solve this problem by anchoring diethylene triamine pentaacetic acid (DTPA) grafted polyethyleneimine (PEI) onto carboxylated GO (GOC-g-PD). Given the amino and carboxyl active groups from PEI and GOC/DTPA, our GOC-g-PD displays good adsorption capacity against not only inorganic metal ions (Cu2+ and Pb2+) but also organic dye (methylene blue: MB). The maximum adsorption capacity of GOC-g-PD for Cu2+, Pb2+ and MB reached 309.60 mg·g−1, 316.17 mg·g−1 and 262.10 mg·g−1, respectively. Furthermore, our GOC-g-PD also exhibits good cycling stability and chemical stability against wide pH values. These outstanding properties revealed our GOC-g-PD held great potential in purifying the sewage discharged from industries. [ABSTRACT FROM AUTHOR]

In the presence of catalytic amounts of molecular iodine and stoichiometric potassium persulfate, a green, highly chemoselective, regioselective and cis-selective radical isothiocyano-chalcogenization of alkenes with NH4SCN in water is disclosed. This three component reaction features high selectivities, an environmentally benign process, mild conditions, high yields, excellent functional-group tolerance, and broad substrate scope. The resulting products can be further transformed into other molecules with structural similarities of these compounds to bioactive analogs. [ABSTRACT FROM AUTHOR]

Chiral sulfones extensively exist in drugs, agricultural chemicals, chiral organic intermediates, and functional materials. Their importance causes the rapid development of their synthetic methods in recent years. Many transition metal complex catalysts with chiral ligands and chiral organocatalysts are adopted in synthesis of chiral sulfones. Most of the methods to construct chiral sulfones are based on the reduction of unsaturated sulfones and the introduction of sulfone groups into unsaturated hydrocarbons. This review describes all classes of asymmetric reactions for synthesis of chiral sulfones. [ABSTRACT FROM AUTHOR]

A transition metal-free synthesis of N-(arylthio/seleno)ethyl sulfoxidmines via blue light-promoted radical sulfoximido-chalcogenization of aliphatic and aromatic alkenes was developed. The sulfoximidation process demonstrated high chemoselectivity and allowed a broad substrate scope, completing the sulfoximido-chalcogenization of alkenes in good yields. [ABSTRACT FROM AUTHOR]

In recent years, multicomponent reactions with inorganic and organic sulfur compounds as one of reactants have achieved a remarkable development. In this review, we summarize recent advances in the multicomponent reactions involving sulfur components, which include elemental sulfur, sodium metabisulfite, sodium hyposulfite, potassium pyrosulfite, DABSO, sodium sulfide, thiocyanate, sulfur dioxide, carbon disulfide and other divalent, tetravalent and hexavalent organosulfur compounds. [ABSTRACT FROM AUTHOR]

Sulfoximines are widely used as medicines, agricultural chemicals, chiral precursors, and chiral ligands in asymmetric synthesis, as well as pivotal intermediates for the construction of heterocyclic compounds. NH‐sulfoximines may be synthesized from thioethers, sulfoxides, sulfilimines, and sulfinamides. NH‐sulfoximines can undergo various transformations, such as arylations, alkylations, vinylations, and alkynylations. Here, we review the methods that have been applied to the syntheses and transformations of NH‐sulfoximines. [ABSTRACT FROM AUTHOR]

A transition-metal-free t -BuOK-mediated reductive C–P cross-coupling reaction of arylvinyl sulfides with diarylphosphine oxides through C–S bond cleavage has been developed. This protocol not only permits the synthesis of diaryl(2-arylethyl)phosphine oxides, but also achieves an unprecedented construction of a C–P bond through C–S bond cleavage and reduction of a C–C double bond in one pot. [ABSTRACT FROM AUTHOR]

A new protocol for the oxidative coupling of ketone oximes with dialkyl/diarylphosphine oxides to synthesize O -(dialkylphosphinyl)ketone oximes has been developed. Hydrogen peroxide is used as a green oxidizing agent, and molecular iodine is used as a nonmetal catalyst. The reaction has a high atom economy, with water as the only byproduct. O -(Dialkylphosphinyl)ketone oximes with 26 examples have been obtained with high yields. Furthermore, the product may be transformed into other molecules, i.e., by reduction. [ABSTRACT FROM AUTHOR]