| Enantioselective conjugate addition of boronic acids to enones catalyzed by O-monoacyltartaric acids. | |
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MedLine Citation:
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PMID: 20852820 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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We have found that O-monoacyltartaric acids catalyze asymmetric conjugate addition of boronic acids to enones with good enantioselectivity, and the 3,5-di(tert-butyl)benzoyl group provides the best results among the acyl groups examined. |
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Authors:
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Masaharu Sugiura; Mirai Tokudomi; Makoto Nakajima |
Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2010-09-20 |
Journal Detail:
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Title: Chemical communications (Cambridge, England) Volume: 46 ISSN: 1364-548X ISO Abbreviation: Chem. Commun. (Camb.) Publication Date: 2010 Nov |
Date Detail:
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Created Date: 2010-10-12 Completed Date: 2011-01-21 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9610838 Medline TA: Chem Commun (Camb) Country: England |
Other Details:
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Languages: eng Pagination: 7799-800 Citation Subset: IM |
Affiliation:
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Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto 862-0973, Japan. msugiura@kumamoto-u.ac.jp |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Alkenes
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chemistry* Boronic Acids / chemistry* Catalysis Ketones / chemistry* Stereoisomerism Substrate Specificity Tartrates / chemistry* |
| Chemical | |
Reg. No./Substance:
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0/Alkenes; 0/Boronic Acids; 0/Ketones; 0/Tartrates; 526-83-0/tartaric acid |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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