Catalytic functionalization of alkynes with organoboron reagents provides a straightforward
access to stereochemically defined multisubstituted alkenes, which are structural motifs …

The use of arylboron reagents in metal‐catalyzed domino addition–cyclization reactions is a
well‐established strategy for the preparation of diverse, highly functionalized carbo‐and …

Achieving complex molecular assemblies in modular modes is always one of the top
priorities of the organic chemist. Cyclization/annulation of functionalized alkynes through …

The development of synthetic methods to produce highly functionalized chiral 3‐pyrrolines is
of indisputable importance because of their prevalence in natural and synthetic bioactive …

A Ni (II)-catalyzed unconventional Meyer–Schuster rearrangement (MSR) is paired with
cross-coupling through inner-sphere acyloxy migration. Various propargyl acetates react …

A nickel-catalyzed reductive desymmetrizing annulation of alkyne-tethered malononitriles
and (hetero) aryl iodides is reported for the access of cyclohexenones containing an α-all …

[4+ 2] oxidative Diels–Alder reaction of readily available alkynols with maleimide is achieved
for the rapid access of pthalimide-fused multicyclic compounds. The reaction is proposed to …

Domino reactions involving nickel‐catalyzed additions of (hetero) arylboronic acids to
alkynes, followed by cyclization of the alkenylnickel intermediates onto tethered acyclic …

Boron-containing organometallic compounds had been always fascinated organic chemists
because it has been widely used in carbon-carbon bond formation reactions such as the …

Enantioselective nickel-catalyzed anti -arylmetallative cyclizations onto acyclic electron-deficient
alkenes - Chemical Communications (RSC Publishing) DOI:10.1039/D1CC01166A Royal …