| Exploring the Unique Reactivity of Diazoesters: An Efficient Approach to Chiral β-Amino Acids. | |
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MedLine Citation:
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PMID: 23323996 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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The development of a highly stereospecific process for the C-O to C-N exchange with retention of configuration is described. This transformation enables access to optically enriched β-amido-α-diazoesters. These products are transformed to β-amino acids not readily accessible using known methods. |
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Authors:
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Barry M Trost; Sushant Malhotra; Pascal Ellerbrock |
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Publication Detail:
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Type: JOURNAL ARTICLE Date: 2013-1-16 |
Journal Detail:
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Title: Organic letters Volume: - ISSN: 1523-7052 ISO Abbreviation: Org. Lett. Publication Date: 2013 Jan |
Date Detail:
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Created Date: 2013-1-17 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 100890393 Medline TA: Org Lett Country: - |
Other Details:
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Languages: ENG Pagination: - Citation Subset: - |
Affiliation:
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Department of Chemistry, Stanford University , Stanford, California 94305-5080, United States. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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