1314243-08-7Relevant articles and documents
Electrochemical Oxidative Cross-Coupling between Vinyl Azides and Thiophenols: Synthesis ofgem-Bisarylthio Enamines
Li, Guodong,Yu, Ke,Yang, Jiajun,Xu, Bo,Chen, Qianjin
, p. 15946 - 15952 (2021/07/20)
An electrochemical radical strategy involving alkene substrates provides a powerful approach for alkene functionalization. Herein, we described the first electrochemical synthesis ofgem-bisarylthio enamines from vinyl azides and thiophenols through the C-
A sustainable strategy for the straightforward preparation of 2H-azirines and highly functionalized NH-aziridines from vinyl azides using a single solvent flow-batch approach
Andresini, Michael,Degannaro, Leonardo,Luisi, Renzo
, p. 203 - 209 (2021/02/26)
The reported flow-batch approach enables the easy preparation of 2H-azirines and their stereoselective transformation into highly functionalized NH-aziridines, starting from vinyl azides and organolithium compounds. The protocol has been developed using c
Zn-ProPhenol Catalyzed Enantioselective Mannich Reaction of 2 H-Azirines with Alkynyl Ketones
Trost, Barry M.,Zhu, Chuanle
, p. 9683 - 9687 (2020/12/21)
The enantioselective Mannich reaction of 2H-azirines with alkynyl ketones is achieved under Zn-ProPhenol catalysis, delivering various aziridines with vicinal tetrasubstituted stereocenters in high yields with excellent enantioselectivities. The bimetalli
