New procedures for selectively protected cholic acid derivatives. Regioselective protection of the 12α-OH group, and t-butyl esterification of the carboxyl group-Reference-Cited by-同舟云学术

New procedures for selectively protected cholic acid derivatives. Regioselective protection of the 12α-OH group, and t-butyl esterification of the carboxyl group

Published:1990 Issue:8 Volume: Page:2245-2250
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Bonar-Law Richard P.,Davis Anthony P.,Sanders Jeremy K. M.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1990/P1/P19900002245

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1. NMR studies of the binding of sodium and calcium ions to the bile salts glycocholate and taurocholate in dilute solution, as probed by the paramagnetic lanthanide dysprosium

2. Potential bile acid metabolites. 8. 7,12-Dihydroxy- and 7.beta.-hydroxy-5.beta.-cholanic acids

3. An approach to bufadienolides from deoxycholic acid-1

4. Synthesis of 3?-Hydroxy[21-14C]-5?-pregn-8(14)-en-20-one from Chenodeoxycholic Acid

5. A very short degradation of the bile acid side chain

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