Formation of lactams via photoelectron-transfer catalyzed reactions of N-allylamines with α,β-unsaturated esters
✍ Scribed by Suresh Das; J.S. Dileep Kumar; Kalchar Shivaramayya; Manapurathu V. George
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- French
- Weight
- 489 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0040-4020
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📜 SIMILAR VOLUMES
The reaction of Ph 3 PסNLi with various ␣,b-unsaturated esters gives access to new N-(␣,b-unsaturated acyl) phosphinimines, which can undergo intramolecular aza-Wittig reactions
e-Acetoxy-8,y-unsaturated nitriles react at room temperature with malonates and acetoacetates in the presence of palladium-phosphine complexes as a catalyst to give y-substituted a,8-unsaturated nitriles selectively. Also yacetoxy-a,8-unsaturated ester was attacked at y-position by malonate.
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