Albicidin is a potent DNA gyrase inhibitor produced by the sugarcane pathogenic bacterium Xanthomonas albilineans. Here we report the elucidation of the hitherto unknown structure of albicidin, revealing a unique polyaromatic oligopeptide mainly composed of p-aminobenzoic acids. In vitro studies provide further insights into the biosynthetic machinery of albicidin. These findings will enable structural investigations on the inhibition mechanism of albicidin and its assessment as a highly effective antibacterial drug.

The heterolytic splitting of hydrosilanes by ruthenium(ii) thiolates is illuminated by a combined spectroscopic, crystallographic, and computational analysis.

The transition-metal-free hydroboration of various alkenes with pinacolborane (HBpin) initiated by tris[3,5-bis(trifluoromethyl)phenyl]borane (BAr ) is reported. The choice of the boron Lewis acid is crucial as the more prominent boron Lewis acid tris(pentafluorophenyl)borane (B(C F ) ) is reluctant to react. Unlike B(C F ) , BAr is found to engage in substituent redistribution with HBpin, resulting in the formation of Ar Bpin and the electron-deficient diboranes [H BAr ] and [(Ar )(H)B(μ-H) BAr ]. These in situ-generated hydroboranes undergo regioselective hydroboration of styrene derivatives as well as aliphatic alkenes with cis diastereoselectivity. Another ligand metathesis of these adducts with HBpin subsequently affords the corresponding HBpin-derived anti-Markovnikov adducts. The reactive hydroboranes are regenerated in this step, thereby closing the catalytic cycle.

NMR investigation of chiral Co(III) salen catalysts, important for enantioselective hydrolytic kinetic resolution (HKR), revealed the presence of a paramagnetic high-spin Co(III) species, which is in solvent- and temperature-dependent equilibrium with the known diamagnetic low-spin Co(III) complex. Combined with quantum chemical DFT calculations, the para- and diamagnetic chemical shifts were used to study the salen ligand conformation of the para- and diamagnetic complexes, resulting in a mechanistic proposal for the enantioselective step in catalysis.