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(Z)-Selective Takai olefination of salicylaldehydes

Authors :
Stephen M. Geddis
Hannah F. Sore
Jonathan M. Goodman
Caroline E. Hagerman
David R. Spring
Warren R. J. D. Galloway
Sore, Hannah [0000-0002-6542-0394]
Goodman, Jonathan [0000-0002-8693-9136]
Spring, David [0000-0001-7355-2824]
Apollo - University of Cambridge Repository
Source :
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 323-328 (2017)
Publication Year :
2017
Publisher :
Beilstein-Institut, 2017.

Abstract

The Takai olefination (or Takai reaction) is a method for the conversion of aldehydes to vinyl iodides, and has seen widespread implementation in organic synthesis. The reaction is usually noted for its high (E)-selectivity; however, herein we report the highly (Z)-selective Takai olefination of salicylaldehyde derivatives. Systematic screening of related substrates led to the identification of key factors responsible for this surprising inversion of selectivity, and enabled the development of a modified mechanistic model to rationalise these observations.

Details

Language :
English
ISSN :
18605397
Volume :
13
Issue :
1
Database :
OpenAIRE
Journal :
Beilstein Journal of Organic Chemistry
Accession number :
edsair.doi.dedup.....9e8cbbf5aa26faaa2d3be540e3f510cd