Eine Reihe von donatorsubstitulerten Monoolefinen addieren sich an Azodlcarbonylverblndungen unter Bildung von Cycloaddukten. Dabei entstehen entweder 1.2-Diazetldine (l,2,3) durch 2+2-oder aber 5,6-Dlhydro-1,3,4-oxadiazine (4,5) durch 2+4-Cycloaddition. Anders als in den bisher bekannten Ftillen e
Konkurrenz zwischen 2+2- und 2+4-cycloaddition bei der umsetzung von p-substituierten arylvinyläthern mit azodicarbonsäuredimethylester
✍ Scribed by Joachim Firl; Sven Sommer
- Book ID
- 104248974
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 203 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
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