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Enantioselective dicarbofunctionalization of (E)-alkenyloxindoles with pyridinium salts by chiral Lewis acid/photo relay catalysis.

Authors :
Zhang, Dong
Dong, Shunxi
He, Qianwen
Luo, Yao
Liu, Yun
Liu, Xiaohua
Feng, Xiaoming
Source :
Chemical Communications. 10/28/2020, Vol. 56 Issue 84, p12757-12760. 4p.
Publication Year :
2020

Abstract

A highly efficient enantioselective dicarbofunctionalization reaction of (E)-alkenyloxindoles with pyridinium salts was realized. The process includes the chiral N,N′-dioxide–Sc(III) complex-catalyzed regio-, diastereo-, and enantioselective [3+2] cycloaddition reaction and the following photo-promoted aza-Norrish II type rearrangement. A series of 2-pyridyl substituted oxindole derivatives were obtained in good yields with moderate to good diastereo- and enantioselectivities. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13597345
Volume :
56
Issue :
84
Database :
Academic Search Index
Journal :
Chemical Communications
Publication Type :
Academic Journal
Accession number :
146582045
Full Text :
https://doi.org/10.1039/d0cc05621a