Palladium-catalyzed stereoselective synthesis of E- and Z-1,1-diaryl or triarylolefins
✍ Scribed by Frédéric Liron; Marina Gervais; Jean-François Peyrat; Mouâd Alami; Jean-Daniel Brion
- Book ID
- 104253323
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 863 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A stereoselective and flexible synthesis of various E-and Z-1,1-diaryl and triarylolefins 3 was achieved from readily available vinylstannanes 1 via stereospecific iodo-destannylation and subsequent palladium-catalyzed Negishi-type cross-coupling reaction with arylzinc reagents under mild conditions.
📜 SIMILAR VOLUMES
## Abstract The palladium‐catalyzed haloallylation of alkynes (I) in dichloromethane leads stereoselectively to (E)‐dihalodienes (III), whereas (Z)‐isomers (IV) are readily obtained by the same reaction in acetic acid in the presence of lithium halides.
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