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(Z)-Selective Takai olefination of salicylaldehydes
- 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.
- Subjects :
- Takai olefination
010405 organic chemistry
Stereochemistry
Chemistry
Organic Chemistry
010402 general chemistry
stereoselectivity
transition state
01 natural sciences
Combinatorial chemistry
salicylaldehydes
0104 chemical sciences
lcsh:QD241-441
chemistry.chemical_compound
Key factors
alkenyl iodides
Salicylaldehyde
lcsh:Organic chemistry
Organic synthesis
lcsh:Q
Selectivity
lcsh:Science
Subjects
Details
- Language :
- English
- ISSN :
- 18605397
- Volume :
- 13
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Beilstein Journal of Organic Chemistry
- Accession number :
- edsair.doi.dedup.....9e8cbbf5aa26faaa2d3be540e3f510cd