Stille coupling of l,l-bis(tri-n-butyistannyl)ethenes proceeds in a stereoselective manner to afford the E-vinylstannanes. Repetition of this sequence affords a new route to tri-substituted alkenes. Intramoleeular Stille coupling of a suitable vin~l bromide affords a pyrmlyl-derived vinylstannane. I
β¦ LIBER β¦
The Reaction of 1,1-Bis(diethylamino)ethene with Phenylmethanesulfonyl Chloride
β Scribed by Truce, William E.; Son, Pyong Nae
- Book ID
- 126968863
- Publisher
- American Chemical Society
- Year
- 1965
- Tongue
- English
- Weight
- 534 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0022-3263
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