| Enantioselective α-hydroxylation of β-ketoamides. | |
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MedLine Citation:
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PMID: 23292494 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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The first enantioselective α-hydroxylation reaction of α-substituted β-ketoamides has been developed by using the commercially available hydroquinine/TBHP system. The tertiary alcohols are obtained in good to high yield and up to 83% ee, which can be improved by a single crystallization. |
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Authors:
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Claudia De Fusco; Sara Meninno; Consiglia Tedesco; Alessandra Lattanzi |
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Publication Detail:
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Type: JOURNAL ARTICLE Date: 2013-1-7 |
Journal Detail:
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Title: Organic & biomolecular chemistry Volume: - ISSN: 1477-0539 ISO Abbreviation: Org. Biomol. Chem. Publication Date: 2013 Jan |
Date Detail:
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Created Date: 2013-1-7 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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Dipartimento di Chimica, Università di Salerno, Via Ponte don Melillo, 84084, Fisciano, Italy. lattanzi@unisa.it. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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