Issue 0, 1971

Retinol analogues. Part I. Synthesis of acyclic analogues of retinoic acid

Abstract

Various C19 analogues of retinoic acid have been prepared from isopropyl t-butyl ketone. Potassium hydrogen sulphate in dimethyl sulphoxide proved an effective reagent for the elimination of water from intermediate hydroxyderivatives, but dehydration of 9-hydroxy-6,10-dimethyl-9-t-butylundeca-3,5,7-trien-2-one yielded 2-methyl-5-(4-isopropyl-1,5,5-trimethylhexa-1,3-dienyl)furan and 9-isopropyl-6,9,10-trimethylundeca-3,5,7,10-tetraen-2-one.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 1878-1884

Retinol analogues. Part I. Synthesis of acyclic analogues of retinoic acid

O. P. H. Augustyn, P. de Wet, C. F. Garbers, L. C. F. Lourens, E. Neuland, D. F. Schneider and K. Steyn, J. Chem. Soc. C, 1971, 1878 DOI: 10.1039/J39710001878

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements