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Short-step Synthesis of Chenodiol from Stigmasterol

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 2004 English Publisher:Oxford University Press (OUP)Journal:Bioscience, Biotechnology, and Biochemistry, volume 68, pages 1,332-1,337 (issn: 0916-8451, eissn: 1347-6947, Copyright policy )
Authors: Toru, Uekawa; Ken, Ishigami; Takeshi, Kitahara;

doi: 10.1271/bbb.68.1332

pmid: 15215599

Short-step Synthesis of Chenodiol from Stigmasterol

Abstract

Chenodiol is an important bile acid widely used for gallstone dissolution and cholestatic liver diseases. We succeeded in a short-step synthesis of chenodiol, starting from the safer phytosterol, stigmasterol.

Related Organizations
Keywords

Molecular Structure, Stigmasterol, Phytosterols, Indicators and Reagents, Chenodeoxycholic Acid, Nuclear Magnetic Resonance, Biomolecular

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
8
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