Conspectus Inter-or intramolecular hydroamination reactions are a paradigmatic example of
modern sustainable organic chemistry, as they are a catalytic, 100% atom-economical, and …

The pyrido [1, 2-a] indole unit found in many organic compounds such as natural products,
pharmaceuticals, and materials, has intensively stimulated the research of new synthetic …

A highly efficient and mild palladium‐catalyzed cross‐coupling of sodium sulfinates and
alkynes for the selective synthesis of unsymmetrical internal alkynes and vinyl sulfones has …

Alkyne hydroamination is an effective approach for the production of enamines and enamine‐
containing N‐heterocycles. However, stereoselectivity control is a considerable challenge in …

A base promoted, protection-free, and regioselective synthesis of highly functionalized
quinolines via [4+ 2] cycloaddition of azadienes (generated in situ from o-aminobenzyl …

The main advances in the chemistry of acetylene in superbasic media achieved over the last
five years are analyzed. Particular emphasis is placed on the ethynylation of aldehydes and …

An intramolecular transition-metal-free base-mediated hydroamination of propargylamine
with isothiocyanates has been achieved. This atom-economical, regioselective …

The endo-cyclic ring closure of 1-(2-(substituted ethynyl) phenyl)-1 H-pyrroles 3a–t and 1-(2-
(substituted ethynyl) phenyl)-H-indole 4a–o mediated by Lewis acid (I2) under mild …

A highly efficient metal and protection-free approach for the regioselective synthesis of C-3-
functionalized quinolines from azadienes (in situ generated from 2-aminobenzyl alcohol) …

Cleavage of Carbon–Carbon Triple Bond: Direct Transformation of Alkynes to Nitriles | Organic
Letters ACS ACS Publications C&EN CAS Find my institution Log In Organic Letters ACS …