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An efficient protocol for the stereoselective construction of multisubstituted fluorine-containing alkenes. a palladium-catalyzed bisstannylation of fluorinated internal alkynes
- Source :
- Journal of Organic Chemistry. Nov 6, 2009, Vol. 74 Issue 21, 8456-8459
- Publication Year :
- 2009
-
Abstract
- The bisstannylation has produced the corresponding bisstannylated cis-adducts by treating various fluorinated internal alkynes with hexabutylditin under the affect of Pd[(t-BuNC).sub.2][Cl.sub.2] in THF at room temperature. These adducts are subjected to the Stille cross-coupling reaction to give the corresponding tetrasubstituted fluorine-containing alkenes with defined stereochemistry.
- Subjects :
- Olefins -- Chemical properties
Olefins -- Structure
Fluorine compounds -- Chemical properties
Fluorine compounds -- Structure
Palladium catalysts -- Chemical properties
Palladium catalysts -- Structure
Tetrahydrofuran -- Chemical properties
Tetrahydrofuran -- Structure
Biological sciences
Chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 00223263
- Volume :
- 74
- Issue :
- 21
- Database :
- Gale General OneFile
- Journal :
- Journal of Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- edsgcl.213841950