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Covering: up to the end of 2022 In recent years rare Actinobacteria have become increasingly recognised as a rich source of novel bioactive metabolites. Actinomadura are Gram-positive bacteria that occupy a wide range of ecological niches. This review highlights about 230 secondary metabolites produced by Actinomadura spp., reported until the end of 2022, including their bioactivities and selected biosynthetic pathways. Notably, the bioactive compounds produced by Actinomadura spp. demonstrate a wide range of activities, including antimicrobial, antitumor and anticoccidial effects, highlighting their potential in various fields. [ABSTRACT FROM AUTHOR]

The synthesis and characterization of a series of Cr(II) N-Heterocyclic Carbene (NHC) complexes of the type [{Cr(NHC)Cl(μ-Cl)}2] and [(Cyp)Cr(NHC)X] (Cyp = η5-C5H5, cyclopentadienyl; η5-C5Me5, pentamethylcyclopentadienyl; X = Cl, η3-C3H5; NHC = IMeMe, IiPrMe, IMes, IDipp) as well as the cyclic (alkyl)(amino)carbene cAACMe ligated complexes [(η5-C5H5)Cr(cAACMe)X] (X = Cl, NPh2), [(η5-C9H7)Cr(cAACMe)Cl] (C9H7 = Ind, indenyl) and [(η5-C13H9)Cr(cAACMe)Cl] (C13H9 = Fl, fluorenyl) are reported. The reduction of [(η5-C5Me5)Cr(IMeMe)Cl] with KC8 in the presence of CO afforded the NHC ligated Cr(I) metallo-radical [(η5-C5Me5)Cr(IMeMe)(CO)2]. Quantum chemical calculations performed on [(η5-C5Me5)Cr(IMeMe)(CO)2] confirm for this complex a predominantly chromium centered radical. [ABSTRACT FROM AUTHOR]

The synthesis and characterization of N-heterocyclic carbene (NHC) and cyclic (alkyl)(amino)carbene (cAAC) complexes of molybdenum(IV) and tungsten(IV) chloride is reported. Reaction of two equivalents of the NHCs IMes (1,3-bis(2,4,6-trimethylphenyl)imidazolin-2-ylidene), IDipp (1,3-bis(2,6-diisopropylphenyl)imidazolin-2-ylidene) and IiPrMe (1,3-diisopropyl-4,5-dimethylimidazolin-2-ylidene) with [MCl4(SEt)2] (M = Mo, W) in toluene afforded the bis-NHC complexes [MCl4(NHC)2] (M = Mo: NHC = IMes 1, NHC = IMes 2; M = W: NHC = IMes 3, NHC = IDipp 4, NHC = IiPrMe5). Mono-carbene complexes [MCl4(NHC)(SEt2)] 6–9 (M = Mo: NHC = IMes 6, NHC = IMes 7; M = W: NHC = IMes 8, NHC = IDipp 9) are available via ligand dismutation of 1–4 with [MCl4(SEt)2]. Complexes 1–9 were characterized by using elemental analysis, IR- and multinuclear NMR spectroscopy and X-ray diffraction for 1–8. The reactivity of the mono-NHC complexes 6–9 towards the cyclic (alkyl)(amino)carbene cAACMe as well as the two electron donor ligands trimethylphosphine, triphenylphosphine, pyridine (py) and N,N-dimethylpyridin-4-amine (DMAP) was studied, which led to the synthesis of the mixed substituted complexes [MCl4(NHC)(cAACMe)] (M = Mo: NHC = IMes 10, NHC = IDipp 11; M = W: NHC = IMes 12, NHC = IDipp 13), [MCl4(NHC)(PR3)] (M = W: NHC = IMes, R = Me 14, NHC = IMes, R = Ph 15, NHC = IDipp, R = Me 16, NHC = IDipp, R = Ph 17), [MCl4(NHC)(py)] (M = Mo: NHC = IMes 18, NHC = IDipp 20; M = W: NHC = IMes 22, NHC = IDipp 24) and [MCl4(NHC)(DMAP)] (M = Mo: NHC = IMes 19, NHC = IDipp 21; M = W: NHC = IMes 23, NHC = IDipp 25). [ABSTRACT FROM AUTHOR]

This frontiers article highlights recent developments of the use of N-heterocyclic silylenes (NHSis), the higher homologues of the Arduengo-carbenes, as ambiphilic activators and ligands in organometallic chemistry and provides a comparison of five-membered ring NHSi ligands with ubiquitous N-heterocyclic carbene (NHC) and phosphine ligands. The frontier orbital region of NHSis differs considerably from that of NHCs which results in different ligation properties. The donor properties of NHSis are closer to those of phosphines than to those of NHCs. NHSis reveal a much stronger tendency to act as bridging ligands between two metal centres than NHCs or phosphines and NHSi insertion reactions into metal–ligand bonds are more facile to achieve compared to similar insertion reactions of NHCs. These interesting properties clearly distinguish NHSi ligands from their NHC or phosphine counterparts and should provide novel reactivities in basic organometallic chemistry and catalysis. [ABSTRACT FROM AUTHOR]

We present herein investigations concerning the reactivity of B2pin2 and FBpin (pin = pinacolato) with respect to fluoride ions and NHCs (NHC = N-Heterocyclic Carbene) in order to understand better the role of added fluoride in our recently reported Ni-catalyzed C–F borylation process, to confirm the nature of the NHC-adducts of FBpin, and to explain the formation of the species detected as side products of the defluoroborylation reaction. We report the calculated gas phase fluoride ion affinities (FIA) of relevant boron species and demonstrate that the presence of one equivalent of added F− in solution will bind and activate B2pin2 (FIA = +247 kJ mol−1), but it will also bind even more effectively to FBpin (FIA = +287 kJ mol−1) formed in the reaction. We prepared the NHC-adducts of FBpin by two different methods and isolated and characterized several examples of the type FBpin·NHC (NHC = iPr2Im, 1; Me2Im, 2; MeiPrIm, 3; nPr2Im, 4; Mes2Im 5). The salts [pinBF2][NMe4] 6, as well as the significantly more soluble analogue [pinBF2][NnBu4] 7, were also isolated and characterized, providing confirmation of the presence of the pinBF2 anion in various stoichiometric and catalytic borylation reactions. [ABSTRACT FROM AUTHOR]

An umpolung strategy for the cross-coupling of polyfluoroarenes with various substituted hydrazones to construct C(sp2)–C(sp3) bonds is developed. In this strategy, the C–F bond of polyfluoroarenes is cleaved and coupled with moisture- and air-stable hydrazones under mild conditions with good to excellent yields. This method provides a useful tool for synthesizing polyfluorinated pharmaceuticals and functional materials. [ABSTRACT FROM AUTHOR]

Covering: 2008 to 2018 This review provides a comprehensive overview of newly discovered natural products containing a tropolonoid motif covering 2008 up to 2018 and depicts the ecological context in which they have been isolated. This review has a strong focus on describing the different analytical tools and molecular biological approaches used to identify the underlying biosynthetic pathways. [ABSTRACT FROM AUTHOR]

A series of rare [NiX2(MeCCprop)] complexes bearing the cis-chelating benzimidazole-derived dicarbene ligand MeCCprop and varying anionic coligands (2, X = N3; 3, X = NCS; 4, X = I; 5, X = O2CCF3) have been prepared and coligand dependent structural and spectroscopic features have been evaluated. This study also revealed an unusual ‘reverse’ carbene transfer reaction from nickel to silver giving the disilver species [Ag2X2(μ–κ2-MeCCprop)] (6, X = OAc; 7, X = O2CCF3). A preliminary catalytic study of two representative NiII diNHC complexes in the aqueous and phosphine-free Suzuki–Miyaura coupling reaction of aryl halides is reported as well. These reactions provide good yields of coupling products, but do not require inert conditions. [ABSTRACT FROM AUTHOR]

The reaction of the silyl complex [Rh{Si(OEt)3}(PEt3)3] (1) with 3,3,3-trifluoropropene afforded the rhodium complex [Rh(CH2CHCF3){Si(OEt)3}(PEt3)2] (2) which features a bonded fluorinated olefin. In contrast the rhodium hydrido complex [Rh(H)(PEt3)3] (3) yielded on treatment with 3,3,3-trifluoropropene in the presence of a base the fluorido complex [Rh(F)(PEt3)3] (4) together with 1,1-difluoro-1-propene by C–F bond activation. At low temperature the intermediate fac-[Rh(H)(CH2CHCF3)(PEt3)3] (5) was detected by NMR spectroscopy. The germyl complex [Rh(GePh3)(PEt3)3] (6) reacted also with 3,3,3-trifluoropropene by C–F bond activation affording again the fluorido complex [Rh(F)(PEt3)3] (4) as well as the (3,3-difluoroallyl)triphenylgermane 7. The catalytic hydrogermylation of 3,3,3-trifluoropropene in the presence of various germanium hydrides under mild conditions was developed by employing complex 6 as a catalyst. The molecular structures of both germane derivatives (3,3-difluoroallyl)triphenylgermane 7 and 1,1,1-trifluoropropane-3-triphenylgermane 8 were determined by X-ray crystallography. [ABSTRACT FROM AUTHOR]