Stereocontrolled Synthesis Of Enantiomerically Pure 2-Dienyl Sulfoxides Via Palladium-Catalyzed Coupling Reactions
Document Type
Article
Publication Date
5-22-1995
Published In
Tetrahedron Letters
Abstract
Enantiopure 2-sulfinyl dienes can be prepared via regio- and stereoselective hydrostannylation of alkynylsulfoxides; after conversion to the corresponding vinyliodides these substrates may be coupled with vinylstannanes via Stille methodology in the presence of BHT.
Recommended Citation
Robert S. Paley, H. L. Weers, P. Fernández, R. F. De La Pradilla, and S. Castro.
(1995).
"Stereocontrolled Synthesis Of Enantiomerically Pure 2-Dienyl Sulfoxides Via Palladium-Catalyzed Coupling Reactions".
Tetrahedron Letters.
Volume 36,
Issue 21.
3605-3608.
DOI: 10.1016/0040-4039(95)00604-B
https://works.swarthmore.edu/fac-chemistry/62