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Journal ArticleDOI

An NMR Technique for Carbon-5 Configurations in 6-Keto-Δ -Steroids

William B. Smith, +1 more
- 01 Apr 1974 - 
- Vol. 23, Iss: 4, pp 579-583
TLDR
In this article, the C-7 proton was used to assess the allylic coupling to the C -5 proton in enol acetates, and the configuration at C-5 in the initial ketone was preserved in the enolacetate, if split into a doublet, then the configuration was α; if a singlet, then it was β.
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This article is published in Steroids.The article was published on 1974-04-01. It has received 2 citations till now. The article focuses on the topics: Enol & Ketone.

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Citations
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Journal ArticleDOI

Fe(II)‐Induced Fragmentation Reaction of γ‐Hydroperoxy‐α,β‐enones. Part 1. Synthesis of 13(14→8)‐abeo‐Steroids

TL;DR: In this article, some steroidal analogues embodying the 13(148)-abeo skeleton have been synthesized by Fe(II)-induced rearrangement (tandem β-fission/reductive alkylation) of 14α-hydroperoxy-7-en-6-ones.
References
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Journal ArticleDOI

Zur Synthese des Ecdysons IX. Mitteilung über Insektenhormone

TL;DR: In this article, a synthesis of ecdysone is described by which the insect moulting hormone can be readily prepared and the side chain was introduced by a Grignard reaction with 2-methyl-3-butyn-2-ol tetrahydropyran-2yl ether and a subsequent reduction of the triple bond.
Journal ArticleDOI

Über einige Eigenschaften von 6‐Keto‐δ7‐Steroiden

TL;DR: In this article, the ORD-, UV- and NMR-spectra of 6-keto-δ7-steroids are discussed and it is shown that there exists a correlation between the configuration of rings A/B and the position of the maxima of the ODE.
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