AbstractÐDeprotonation of Boc-protected amines with sec-BuLi or transmetallation of a-aminostannanes with n-BuLi affords a-aminoalkyllithium reagents which can be converted into a-aminoalkylcuprate reagents with CuCN or THF soluble CuCN´2LiCl. These reagents undergo conjugate addition reactions with
New methods for β-conjugate addition and β-hydroxyalkylation of enones
✍ Scribed by Sunggak Kim; Phil Ho Lee
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 223 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
S-Conjugate addition and 5-hydroxyalkylation of enones have been accomplished by the reaction of ylides, derivated from enones via phosphoniosilylation, with activated olefins and aldehydes in the presence of trimethylsilyl triflate in tetrahydrofuran at -78 OC and subsequent elimination of phosphonium salts by one-pot procedure.
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
Reaction of indoles with electron deficient olefins under the influence of bismuth triflate has been studied at ambient temperature and affords the corresponding 3-alkylated indoles in excellent yields.