Cycloaddition of. Diphenylketene to Some C=N Heterocycles. Structural Assignment and Reactions of Adducts

Makhluf J. Haddadin, Alfred Hassner

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

The cycloaddition reactions of diphenylketene to some C=N heterocycles have been reexamined and the adducts are assigned oxazinone (3 or 4) rather than amido ketone structures 2. The reaction of 4 with hydrazine yielded pyrazolinone 7, whereas sodium methoxide produced the ring-opened ester 6.

Original languageEnglish
Pages (from-to)2650-2652
Number of pages3
JournalJournal of Organic Chemistry
Volume38
Issue number15
DOIs
StatePublished - 1 Jul 1973
Externally publishedYes

Fingerprint

Dive into the research topics of 'Cycloaddition of. Diphenylketene to Some C=N Heterocycles. Structural Assignment and Reactions of Adducts'. Together they form a unique fingerprint.

Cite this