Issue 0, 1979

Chemistry of amine–boranes. Part 5. Reduction of oximes, O-acyloximes, and O-alkyl-oximes with pyridine–borane in acid

Abstract

Oximes, O-acyl-oximes, and O-alkyl-oximes were reduced with pyridine–borane in the presence of acid to the corresponding hydroxylamine derivatives without over-reduction. Unstable O-acyl-hydroxylamines were directly synthesized for the first time from the corresponding O-acyl-oximes.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1979, 643-645

Chemistry of amine–boranes. Part 5. Reduction of oximes, O-acyloximes, and O-alkyl-oximes with pyridine–borane in acid

M. Kawase and Y. Kikugawa, J. Chem. Soc., Perkin Trans. 1, 1979, 643 DOI: 10.1039/P19790000643

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