Diels-alder cycloaddition reactions of αβ-unsaturated aldehyde acylhydrazones
✍ Scribed by Sylvia J. Allock; Thomas L. Gilchrist; Frank D. King
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 232 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
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).
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## Abstract For Abstract see ChemInform Abstract in Full Text.
Diels-Alder Reactions of α,β-Unsaturated Thioesters and α,β-Unsaturated Selenoesters. -The regio-and exo/endo-selectivity of Diels-Alder reactions of thio-and selenoesters (II) with dienes is investigated. In general, thermal reactions show only low selectivities as expected. The selectivity improv