885722-38-3Relevant academic research and scientific papers
Substrate-controlled and site-selective [3+2] cycloadditions of N-heterocyclic carbene derived ambident dipoles
Cheng, Ying,Liu, Mei-Fang,Fang, De-Cai,Lei, Xue-Mei
, p. 4282 - 4292 (2008/02/08)
2-Aryl thiocarbamoyl benzimidazolium and imidazolinium inner salts derived from benzimidazole and imidazoline carbenes are unique ambident C-C-S and C-C-N 1,3-dipolar systems, which undergo highly efficient and site-selective cycloaddition reactions with
A N-heterocyclic carbene derived highly regioselective ambident C-C-S and C-C-N 1,3-dipolar system
Liu, Mei-Fang,Wang, Bo,Cheng, Ying
, p. 1215 - 1217 (2008/02/03)
N-Heterocyclic carbene derived 2-phenylthiocarbamoyl benzimidazolium and imidazolinium inner salts are a unique ambident C-C-S and C-C-N 1,3-dipolar system able to undergo highly efficient and regioselective cycloaddition with dimethyl acetylenedicarboxyl
