Influence of the solvent ability to form hydrogen bonds in the crystal structure of ([3β,5β,7α,12α]-3[(norbornyl-2-acetyl)-amino]-7,12-dihydroxycholan-24-oic acid (a norbornyl derivative of cholic acid)-Reference-Cited by-同舟云学术

Influence of the solvent ability to form hydrogen bonds in the crystal structure of ([3β,5β,7α,12α]-3[(norbornyl-2-acetyl)-amino]-7,12-dihydroxycholan-24-oic acid (a norbornyl derivative of cholic acid)

Published:2009-09 Issue:9 Volume:74 Page:735-741
ISSN:0039-128X
Container-title:Steroids
language:en
Short-container-title:Steroids

Author:

Miragaya Javier,Jover Aida,Fraga Francisco,Meijide Francisco,Tato José Vázquez

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry

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4. Functional monomers and polymers. XXXIX. Synthesis of optically active poly(trans-2-methylpentadiene) by asymmetric inclusion polymerization in deoxycholic acid;Miyata;Polym J,1977

5. Functional monomers and polymers. 161. Inclusion polymerization in deoxycholic acid and apocholic acid canals: decisive role of a relative size between a canal and a monomer;Miyata;Makromol Chem Rapid Commun,1988

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