One pot synthesis of 2-vinyl-1-azadienes and divinylketones
✍ Scribed by José Barluenga; Isabel Merino; Francisco Palacios
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 224 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
## Abstract A synthetic route that allows modification of 1‐vinyl‐2‐pyrrolidone with an alcohol or thiol group in its 3‐position in a one‐pot reaction without using protecting groups is described. The strategy used to achieve this goal is the reaction of the carboxamide anion of 1‐vinyl‐2‐pyrrolido
1997 organo-selenium compounds, isocyclic C derivatives organo-selenium compounds, isocyclic C derivatives S 0134 ## 25 -172 Convenient One-Pot Synthesis of Vinyl Selenides. -A convenient one-pot procedure for the synthesis of vinyl selenides ( IV) (7 examples) based on a modified Horner-Emmons r