Characterizationf of autoxidation products of retinoic acid

A. R. Oyler, M. G. Motto, R. E. Naldi, K. L. Facchine, P. F. Hamburg, D. J. Burinsky, R. Dunphy, M. L. Cotter

Research output: Contribution to journalArticlepeer-review

37 Scopus citations

Abstract

Retinoic acid underwent autoxidation in 90% ethanol at 25-85.5 °C to give epoxides, dioxetanes, an endoperoxide, and double-bond cleavage products. The majority of these products appear to have resulted from the initial direct oxidation of the olefinic carbons rather than from the expected allylic α oxidation process.

Original languageEnglish (US)
Pages (from-to)7679-7694
Number of pages16
JournalTetrahedron
Volume45
Issue number24
DOIs
StatePublished - 1989

Fingerprint Dive into the research topics of 'Characterizationf of autoxidation products of retinoic acid'. Together they form a unique fingerprint.

Cite this