Solution conformation of three steroid 19-nor-4-en-3-ones determined from two-dimensional nuclear magnetic resonance spectroscopy, coupling constant calculations, and circular dichroism-Reference-Cited by-同舟云学术

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Solution conformation of three steroid 19-nor-4-en-3-ones determined from two-dimensional nuclear magnetic resonance spectroscopy, coupling constant calculations, and circular dichroism

Published:1988 Issue:5 Volume: Page:765-771
ISSN:0300-9580
Container-title:J. Chem. Soc., Perkin Trans. 2
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 2

Author:

Wong Tuck C.,Guo Wei,Bohl Martin,Hübner Michael,Luck Gerhard,Steiger Thomas,Reck Gunter

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1988/P2/P29880000765

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Angular dependence of spin–spin coupling constants;Progress in Nuclear Magnetic Resonance Spectroscopy;2000-11-27

2. 1H–1H long range couplings in fused cyclopropanes. NMR spectral assignment and conformation of 17,18-cyclosteroids;J. Chem. Soc., Perkin Trans. 2;1996

3. Advances in Theoretical and Physical Aspects of Spin-Spin Coupling Constants;Annual Reports on NMR Spectroscopy;1993

4. Conformational analysis of ring A and total assignment of 19-functionalized 4-en-3-one steroids. Applicability of 2D NOE as a crucial technique;The Journal of Organic Chemistry;1991-07

5. Conjugation of spirocyclopropane with the carbonyl group. Conformational analysis of spiro [cyclopropane-1,2′-steroids];Magnetic Resonance in Chemistry;1991-02

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