Cleavage vs. Beckmann Rearrangement in α-Oximino Ketones

Alfred Hassner, W. A. Wentworth, I. H. Pomerantz

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

Certain cyclic α-oximino ketones under Beckmann rearrangement conditions yield the expected rearrangement products (imides), but it can be shown that the reaction proceeds first by cleavage followed by ring closure to the imides.

Original languageEnglish
Pages (from-to)304-306
Number of pages3
JournalJournal of Organic Chemistry
Volume28
Issue number2
DOIs
StatePublished - 1 Feb 1963
Externally publishedYes

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