Journal article
Unsaturated nitriles: Optimized coupling of the chloroprene Grignard reagent with omega-brominitriles
Journal of organic chemistry, Vol.62(22), p7890
31 Oct 1997
Abstract
The Diels-alder reaction is a powerful organic synthesis reaction. An effective synthesis of dienes for type II intramolecular Diels-Alder (IMDA) reactions involves coupling electrophiles with 1-methylene-2-propenylmagnesium chloride, or chloroprene Grignard reagent. The coupling of 1-methylene-2-propenylmagnesium chloride with omega-bromonitriles achieved good yields of unsaturated nitriles.
Metrics
3 Record Views
Details
- Title
- Unsaturated nitriles: Optimized coupling of the chloroprene Grignard reagent with omega-brominitriles
- Creators
- Fraser F FlemingTao Jiang
- Publication Details
- Journal of organic chemistry, Vol.62(22), p7890
- Publisher
- American Chemical Society
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Chemistry
- Identifiers
- 991020898500304721