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pubmed-article:12441189pubmed:dateCreated2002-11-20lld:pubmed
pubmed-article:12441189pubmed:abstractTextWe describe the synthesis of (25R)-cholest-5-en-3beta,26-diol ((25R)-26-hydroxycholesterol) from diosgenin in four steps in 58% overall, yield via a modified Clemmensen reduction followed by a Barton deoxygenation reaction.lld:pubmed
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pubmed-article:12441189pubmed:authorpubmed-author:WilliamsJohn...lld:pubmed
pubmed-article:12441189pubmed:authorpubmed-author:ChaiDepingDlld:pubmed
pubmed-article:12441189pubmed:authorpubmed-author:WrightDominic...lld:pubmed
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pubmed-article:12441189pubmed:pagination1041-4lld:pubmed
pubmed-article:12441189pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:12441189pubmed:articleTitleSynthesis of (25R)-26-hydroxycholesterol.lld:pubmed
pubmed-article:12441189pubmed:affiliationDepartment of Chemistry, Temple University, 13th & Norris Streets, Beury Hall (016-00), Philadelphia, PA 19122-2585, USA. john.r.williams@temple.edulld:pubmed