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Lettuce (Lactuca sativa) is one of the most important vegetable crops in the world. As a leafy vegetable, the polymorphism of lettuce leaves from dark to pale green is an important trait. However, the genetic and molecular mechanisms underlying such variations remain poorly understood. In this study, one major locus controlling the polymorphism of dark- and pale-green leaves in lettuce was identified using genome-wide association studies (GWAS). This locus was then fine mapped to an interval of 5375 bp on chromosome 4 using a segregating population containing 2480 progeny. Only one gene, homologous to the GLK genes in Arabidopsis and other plants, is present in the candidate region. A complementation test confirmed that the candidate gene, LsGLK, contributes to the variation of dark- and pale-green leaves. Sequence analysis showed that a CACTA transposon of 7434 bp was inserted 10 bp downstream of the stop codon of LsGLK, followed by a duplication of a 1826-bp fragment covering exons 3-6 of the LsGLK gene. The transposon insertion did not change the expression level of the LsGLK gene. However, because of alternative splicing, only 6% of the transcripts produced from the transposon insertion were wild-type transcripts, which led to the production of pale-green leaves. An evolutionary analysis revealed that the insertion of the CACTA transposon occurred in cultivated lettuce and might have been selected in particular cultivars to satisfy the diverse demands of consumers. In this study, we demonstrated that a transposon insertion near a gene may affect its splicing and consequently generate phenotypic variations.

A family of axially chiral azepine-containing seven-membered cyclic P,N-ligands (named Indole-azepinap) have been prepared by using l-alanine as an original chirality source. The direct chromatographic separation of two diastereomeric phosphine oxides on silica gel enabled these ligands to be easy available, allowing further structural and electronic modifications. Preliminary application of these Indole-azepinaps has been demonstrated in a Pd-catalyzed asymmetric allylic alkylation with high yields and moderate enantioselectivities.

Reductive elimination of alkyl-Pd

Classical Julia–Kocienski fluoroolefination represents an indispensable platform for the construction of monofluoroalkenes. Nevertheless, its complex multistep mechanistic manifold along with the u...

Two approaches involving intramolecular and intermolecular cyclization, respectively, have been developed for the direct and practical construction of a series of important benzo[f]pyrrolo[1,2-a][1,4]azepines by using Brønsted acid catalysts. Upon catalysis by TsOH, the intramolecular dehydroxylation/ring closure of 3-hydroxy-2-[2-(1H-pyrrol-1-yl)benzyl]isoindolin-1-ones provided various racemic benzo[f]pyrrolo[1,2-a][1,4]azepines in high yields. Furthermore, enantioenriched benzo[f]pyrrolo[1,2-a][1,4]azepines were also obtained by chiral phosphoric acid catalyzed intermolecular addition of [2-(1H-pyrrol-1-yl)phenyl]methanamines to 2-formylbenzoates under mild conditions.

A novel intramolecular Smiles rearrangement of α-fluoro-β-keto-pyrimidylsulfones (usually used as a carbon nucleophile) was developed, providing a versatile avenue for synthesis of tri/tetra-substituted monofluorinated pyrimidyl enol ethers. Among these, diverse (Z)-monofluorovinylsulfones and sulfinates were efficiently assembled by adding extra electrophile and fine-tuning reaction conditions. The process is triggered by a keto-enol tautomerism from enol oxyanion to pyrimidine 2-carbon, completely different from the classical carbon nucleophilic addition reaction approach.

A family of axially chiral quinazolinone-based heterobiaryls were constructed with high levels of enantiocontrol (up to 94% ee). Convergently, three different synthetic methods have been realized to prepare these valuable compounds including central-to-axial chirality transfer, dynamic kinetic resolution, and phase-transfer catalysis. Importantly, novel P,N-ligands with a π-π stacking can be derived from heterobiaryls by chirality exchange strategy or synthesized directly from complementary phase-transfer catalysis by using the inexpensive chiral quaternary ammonium salt.

A novel process involving base-catalyzed intramolecular defluorination/O-arylation of readily available α-fluoro-β-one-sulfones was realized and provided a series of 3-fluoro-1,4-oxathiine 4,4-dioxide derivatives in good to excellent yields. Unlike traditional defluorination reactions with stoichiometric base as the deacid reagent, this process is triggered by a catalytic amount of base (TMG: tetramethylguanidine) and molecular sieves serve as both an adsorbent to remove HF acid and an activator to assist C–F bond cleavage.

Central-to-axial chirality transfer via C-N single bond oxidation was first achieved as a versatile and conceptually distinct strategy to prepare a new family of axially chiral heteroaromatic biaryl backbones and P,N-ligands (named as Quinoxalinaps) in gram scale. Two atropisomers of Quinoxalinaps (ee >99%) were readily accessed from the same precursor enantiomer by a simple dehydrogenative oxidation with MnO2 and t-BuOOH under mild conditions. Phosphine could be introduced into the ligands before or after the chirality control process. Moreover, these Quinoxalinap P,N-ligands performed well for both asymmetric reactions of the CuBr-catalyzed alkyne conjugate addition with up to -94% ee and AgOAc-catalyzed glycinate imine [3 + 2] annulation with 90% ee, respectively.

Lettuce (Lactuca sativa) is one of the most important vegetables worldwide and an ideal plant for producing protein drugs. Both well-functioning chloroplasts that perform robust photosynthesis and small leaf angles that enable dense planting are essential for high yields. In this study, we used an F

A novel process involving Grignard-reagent-promoted desulfonylation/intramolecular coupling of readily available α-fluoro-α,β-unsaturated-(2-pyridyl)sulfones was realized that provided a series of polysubstituted 2-(1-fluorovinyl)pyridines in good yields. The intrinsic coordination between pyridine and Mg(II) along with the "negative fluorine effect" of the substrates should play the key role for the smooth transformation in the absence of transition-metal catalysts.

Reported is a unique chemoselectivity approach to base-promoted defluorinative and Cu(i)-catalyzed aerobic oxidative non-defluorinative [5 + 1] condensation aromatizations of simple unsaturated ketones with ammonium salts via Meisenheimer-type nitrogen anion and radical intermediates. The CuBr/O2 catalysis provides a straightforward approach to diverse 3-fluoropyridines in high yields. The synthetic utility of the strategy is highlighted by the concise synthesis of several F-modified bioactive compounds.

With the rapid development of China’s high-speed railway, the scale and complexity of railway signal software are increasing, and efficient and sufficient testing has played an important role in improving software security and reducing railway safety accidents. As the core equipment of railway signal, computer-based interlocking system is mainly manual testing, which is inefficient and inadequate. In order to improve the safety of interlocking system, it is urgent to strengthen the research of testing technology and method. Therefore, after the research and analysis of computer-based interlocking system and its testing, this paper puts forward some improved testing methods and strategies of interlocking software, and designs the corresponding automatic test platform. We have carried out in-depth research on the functions of the platform, as well as the key technologies and difficulties of the platform construction, in order to improve the adequacy and accuracy of the testing, to improve the safety of the interlocking software, and thus ensure the safety of railway transportation.

Despite the widespread use of naphthamide atropisomers in biologically active compounds and asymmetric catalysis, few catalytic methods have succeeded in the enantioselective synthesis of these compounds. Herein, a chiral Bronsted acid (CBA) catalysis strategy was developed for readily scalable dynamic kinetic resolution of challenging ortho-formyl naphthamides with pyrrolylanilines. The chiral axis of the atropisomeric amide and a stereogenic center were simultaneously established for a new family of potential biologically active pyrrolopyrazine compounds with high enantio- and diastereoselectivities (up to >20 : 1 d.r. and 98 : 2 e.r.). Epimerization experiments of its derivatives reveal that the N-substitution of the nearby stereogenic center could affect the configurational stability of the axially chiral aromatic amides. These results might be useful for the construction of other kinds of novel axially chiral molecules with a low rotational barrier.

The Tieshanmiao hosted by the metamorphosed Paleoproterozoic Upper Taihua Group, is a large-scale BIF–hosted Fe deposit in the southern margin of the North China Craton. The formation age, BIF type, depositional condition as well as the genesis of pyroxene–rich BIF is under heated debate. In this study, we present petrology, whole–rock geochemistry, zircon U–Pb geochronology and Lu–Hf isotope analyses on the Tieshanmiao Fe deposit. The Fe ore of the deposit can be divided into two sub-types, including banded pyroxene–magnetite quartzite (BMQ) and disseminated magnetite pyroxenite (DMP). The hanging wall rock pyroxene biotite gneiss yields an upper intercept age of 2406 ± 24 Ma, interpreted as the lower limited age for BIF deposition. The foot wall rock garnet–bearing biotite plagioclase gneiss yields a weighted mean 207Pb/206Pb age of 2739 ± 12 Ma, interpreted as its maximal depositional age. Lu-Hf isotope systematics indicates that pyroxene biotite gneiss is derived from the Paleoproterozoic mantle contaminated by the crust, and the provenance of garnet–bearing biotite plagioclase gneiss is derived from a Mesoarchean crust. The primary mineral assemblages of the pyroxene–rich Tieshanmiao Fe deposit are Fe–silicate, Ca/Mg–carbonate, ferrihydrite, and minor quartz. The BMQs have high and variable Y/Ho ratios (40–80), recording periodic alkaline hydrothermal injection that is progressively diluted by seawater, while the DMPs have low and constrained Y/Ho ratios, archiving well–supplied alkaline hydrothermal injection. We propose a REY (lanthanide elements and Y) modelling of multi–Fe sources for the Tieshanmiao BIF deposit. The BMQs are sourced from seawater and high–T hydrothermal fluid, while the DMPs are sourced from seawater, high–T hydrothermal fluids and one or several additional Fe fluxes (e.g. high-Fe dissolved riverine fluxes, low–T hydrothermal fluids or benthic Fe shuttles driven by dissimilatory iron reduction). The basic gneisses as metabasalts associated with the Tieshanmiao Fe deposit are characterized by high–Fe assay, variable LREE enrichment, relatively depletion in Nb, Ta, Zr, Ti, Y, and Th. The geochemistry of the basic gneisses shows affinities to both MORBs and volcanic–arc basalts, indicating a back–arc basin setting of the BIF deposition. It is most likely a Superior–type BIF–hosted Fe deposit, which is formed in a back–arc basin along the craton–side continental shelf.

A new method for CF3SO2Na-based direct trifluoromethylthiolation of C(sp(2))-H bonds has been developed. CF3SSCF3 is generated in situ from cheap and easy-to-handle CF3SO2Na, and in the presence of CuCl can be used for electrophilic trifluoromethylthiolation of indoles, pyrroles, and enamines. The method has been extended to perfluoroalkylthiolation reactions using RfSO2Na.

The highly stereoselective olefination reaction of α-fluoro-β-keto esters for the synthesis of α-fluoro-α,β-unsaturated esters has been developed. The olefination combines nucleophilic addition, intramolecular nucleophilic addition, and elimination in one step, as well as provides a facile synthetic approach to α-fluoro-α,β-unsaturated esters which are important units in many biologically active compounds and useful precursors in a variety of functional-group transformations.

A simple and convenient tandem reaction of α-ketoesters with primary or secondary aromatic amines for the synthesis of polysubstituted 1,2-dihydroquinolines has been developed. The catalytic system (fluorous hydrazine-1,2-bis(carbothioate)/NCS) of the reaction has the advantages of operational simplicity, high efficiency, as well as easy recyclability.

Di-tert-butyl peroxide can smoothly promote the coupling of aryl halides with benzene derivatives without the aid of transition-metal catalysts through a chain homolytic aromatic substitution mechanism in the presence of potassium tert-butoxide.

A new method for CF3SO2Na-based direct trifluoromethylthiolation of C(sp(2))-H bonds has been developed. CF3SSCF3 is generated in situ from cheap and easy-to-handle CF3SO2Na, and in the presence of CuCl can be used for electrophilic trifluoromethylthiolation of indoles, pyrroles, and enamines. The method has been extended to perfluoroalkylthiolation reactions using RfSO2Na.

A new strategy for the synthesis of differently substituted phenols is established through one-pot Robinson annulation of α-fluoro-β-ketoesters with α,β-unsaturated ketones followed by in situ dehydrofluorination and tautomerization.

A new strategy for the synthesis of 3,5-disubstituted phenols is established through one-pot Robinson annulation of α,β-unsaturated ketones with α-fluoro-β-ketoesters followed by in situ dehydrofluorination and tautomerization. This method has been extended to the synthesis of polysubstituted phenols and applied in the preparation of biologically active compounds.

A new fluorous imine carbothioate has been prepared as an organocatalyst for the synthesis of pyrrol-2-ones via the cyclo-condensation reaction of aldehydes, amines, and pyruvate at room temperature. The fluorous catalyst can be easily recovered from the reaction mixture by simple fluorous solid-phase extraction (F-SPE) and used for next run reaction without further purification.

A new fluorous carbothioate acts as a catalyst in the synthesis of pyrrolones via cyclocondensation of aldehydes, pyruvate, and amines.

Due to feedback delay, the capacity of water filling power allocation will degrade, even worse than the fixed power allocation. This problem may be more serious when mobile terminal moves at high velocity, for example in high-speed train. Through analysis of the distance correlation properties of shadow fading, this paper presents an improved water-filling power allocation approach, which adjusts power allocation according to feedback delay. Simulation results show that the proposed approach can improve capacity of shadow fading channel with delayed feedback and satisfies power constraint.

In this paper, we discuss the channel characteristics on high-speed railway and discuss the ergodic and outage capacity for Ricean channel with shadow fading. The impacts of dynamic K factor on ergodic and outage capacity are evaluated too. Simulation results show both shadow fading and dynamic K factor have significant impact on outage capacity, but little impact on ergodic capacity.