Metal-catalyzed highly Markovnikov-type selective hydrofunctionalization of terminal alkynes
provides a straightforward and atom-economical route to access 1, 1-disubstituted alkenes …

Herein, we have developed an efficient and green method for the synthesis of various alkyl
amines via the C (sp3)–S bond cleavage of vinylsulfonium salts. The reaction proceeds …

Herein, we report a facile and efficient synthetic method to construct azepino [1, 2-a] indoles
through a novel gold (I)-catalyzed intramolecular hydroarylation of alkynylindoles. A wide …

Herein, we describe a convenient protocol for the synthesis of N-alkenylated heterocycles
using abundant ketone electrophiles and T3P as a water scavenger under microwave …

A protocol for the synthesis of terminal N‐vinylazoles from aromatic aldehydes, DMSO, and
azoles has been reported. In this strategy, DMSO was involved in the construction of the C …

The Zn (OTf) 2-catalyzed hydroamination of ynamides 2a–2l with aromatic amines 1a–1r
was developed. This protocol features broad substrate scope of aromatic amines, good …

N-Vinylcarbazoles are important skeletons for photoluminescent materials. Herein, a
transition metal-free, B (C6F5) 3 mediated carbazolation reaction of alkynes is reported …

The effect of chemical element on the reactivity for carbazolation reaction of phenylacetylene
utilizing G13 (C6F5) 3 (Lewis acid) and G15-carbazole (Lewis base) was theoretically …

Herein, we report a reaction protocol for the construction of benzo [a] carbazole and dibenzo
[c, g] carbazole frameworks. The detailed gold catalytic reaction conditions developed for the …

A Cu (I)‐catalyzed three‐component reaction of 2‐iodo‐2, 2‐difluoroacetophenones,
alkynes, and TMSCN is described. The reaction provided a facile method for the synthesis of …