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Search for a Nonelectrocyclic Cyclization of Nitrosostyrene: Rearrangements of Michael Adducts from DMAD and a-Dialkylamino Oximes
Nonelectrocyclic Cyclization of Nitrosostyrene DMAD a-Dialkylamino Oximes
2010/4/21
The aza-Claisen rearrangement product of the Michael adducts 2 from a-dialkylaminoacetophenone oximes and DMAD underwent fragmentation to give dialkylaminomaleate, and benzonitrile at reflux in aceton...