Synthesis of 3β,14-dihydroxy-5β,14β-pregnan-20-one C-3 derivatives: ozonolysis of digitoxin and digitoxigenin and their derivatives followed by zinc–acetic acid reduction to the C-21 methyl ketone-Reference-Cited by-同舟云学术

Synthesis of 3β,14-dihydroxy-5β,14β-pregnan-20-one C-3 derivatives: ozonolysis of digitoxin and digitoxigenin and their derivatives followed by zinc–acetic acid reduction to the C-21 methyl ketone

Published:1991 Issue:4 Volume: Page:823-829
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Templeton John F.,Ling Yangzhi,Jin Jichun,Boehmer Mark A.,Zeglam Talal H.,LaBella Frank S.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1991/P1/P19910000823

Reference27 articles.

1. Cardiac glycoside-like structure and function of 5.beta.,14.beta.-pregnanes

2. Digitalis-like pregnanes. Cardiac and renal effects of a glycoside of 14β-hydroxyprogesterone

3. Progesterone derivatives that bind to the digitalis receptor: synthesis of 14.beta.-hydroxyprogesterone: a novel steroid with positive inotropic activity

4. Ozonolyse von Diacetylgitoxigenin Untersuchung des Verlaufs der alkalischen Hydrolyse bei einigen 14?-Hydroxy�tians�uren und ihren Methylestern I. Mitteilung

5. Ozonolyse von Di-O-acetyl-gitoxigenin. II. Mitteilung

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