Amidyl and carbamyl radicals by stannane mediated cleavage of O-benzoyl hydroxamic acid derivatives

Research output: Contribution to journalArticlepeer-review

Abstract

O-Benzoyl hydroxamic acids react with tributylstannane in the presence of AIBN to give amidyl or carbamyl radicals which can be captured by an internal olefin.

Original languageEnglish
Pages (from-to)6109-6112
Number of pages4
JournalTetrahedron Letters
Volume35
Issue number33
DOIs
Publication statusPublished - 15 Aug 1994
Externally publishedYes

Fingerprint

Dive into the research topics of 'Amidyl and carbamyl radicals by stannane mediated cleavage of O-benzoyl hydroxamic acid derivatives'. Together they form a unique fingerprint.

Cite this