TítuloFerrocenylindium reagents in palladium‐catalyzed cross‐coupling reactions: asymmetric synthesis of planar chiral 2‐aryl oxazolyl and sulfinyl ferrocenes

In this work, we describe the catalytic asymmetric synthesis of chiral BODIPY cyclohexane derivatives, using trienamine aminocatalysis via a Diels–Alder reaction (Scheme 1c)..

Herein we describe a robust and practical method to prepare enantiomerically enriched trisubstituted allenes using alkyl Grignard reagents and bench stable

In summary, we have developed the first catalytic enantioselective synthesis of cyclobutylboronates, catalyzed by a chiral phosphine-copper(I) complex. The method

active esters, which have been successfully used in simple Ni- catalyzed cross-coupling reactions, [7] and to take advantage of the presence of an alkene to realize a cyclization,

Fidelity of Human Immunodeficiency Viruses Type 1 and Type 2 Reverse Transcriptases in DNA Synthesis Reactions using DNA and RNA Templates... Universidad Autónoma de Madrid

Pioneering work has been recently reported on the asymmetric α-allylation of carbonyl compounds [17–27], α-fluorination of acyl derivatives [28–30], decarboxylative protonation

Importantly, this alkenylation method seems to be not very sensitive to steric hindrance imposed by aryl ortho-substitution, as illustrated in smooth reaction

Moreover, the enallene 70 used by Bäckvall and coworkers, 241f was also subjected to the reaction conditions giving rise to a mixture of three alkylboronates (71) located around