| Synthesis and revision of stereochemistry of rubescensin S. | |
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MedLine Citation:
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PMID: 21584305 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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An effective two step transformation of oridonin to 15,16-seco-ent-kaurane skeleton is reported. We also achieved the conversion of one intermediate to natural product rubescensin S and revised its structure as a 13S configuration although 13R is reported in the literature. |
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Authors:
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Mei Zhang; Yangming Zhang; Wei Lu; Fa-Jun Nan |
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Publication Detail:
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Type: JOURNAL ARTICLE Date: 2011-5-16 |
Journal Detail:
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Title: Organic & biomolecular chemistry Volume: - ISSN: 1477-0539 ISO Abbreviation: - Publication Date: 2011 May |
Date Detail:
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Created Date: 2011-5-17 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 101154995 Medline TA: Org Biomol Chem Country: - |
Other Details:
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Languages: ENG Pagination: - Citation Subset: - |
Affiliation:
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Department of Chemistry and Institute of Medicinal Chemistry, East China Normal University, 3663 North Zhong Shan Road, Shanghai, 200062, China. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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