Issue 8, 1990

Oximation of 2-azido-4,4-dimethyl-3-oxo steroids: formation of α-keto oximes and dioximes

Abstract

Treatment of 2-azido-4,4-dimethyl-3-oxo steroids (1a, b) with an excess of hydroxylamine hydrochloride in the presence of sodium acetate give the corresponding 2α-azido-3-hydroxyimino (2a, b) and 2,3-bishydroxyimino derivatives (3a, b). In the case of the Δ5-analogue (1c), the 2-hydroxyimino-3-oxo compound (4c) is formed in addition to the 2-azido-3-hydroxyimino (2c) and 2,3-bishydroxyimino (3c) derivatives. The bishydroxyimino compounds (3) were converted into the oxadiazole (furazan) derivatives (6).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 2277-2280

Oximation of 2-azido-4,4-dimethyl-3-oxo steroids: formation of α-keto oximes and dioximes

T. T. Takahashi, J. Y. Satoh and K. Saitoh, J. Chem. Soc., Perkin Trans. 1, 1990, 2277 DOI: 10.1039/P19900002277

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