Cycloadditions of diazoesters to α,β-unsaturated aldehydes
✍ Scribed by A.F. Noels; J.N. Braham; A.J. Hubert; Ph. Teyssié
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- French
- Weight
- 236 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Pyridine 9b was isolated in 92% yield and had np. 'te 1W19loC). 10 11 The phenylhydmzone. 2,4dinitrophenylhydrszone and tosylhydrazone of methacrolein also react with Nphenylmaleimide as 1-azadienes (experiments by S. J. Shuttlewotth).
## Abstract For Abstract see ChemInform Abstract in Full Text.
The oxidation of aldehydes to a@-unsaturated aldehydes has been performed by a sequence of reactions involving conversion into aldimines, chlorination at the a-position to form a-chloroaldimines, base-induced dehydrochlorination and h drol sis The four-step transformation can be executed without iso