| Catalytic asymmetric protonation of alpha-amino acid-derived ketene disilyl acetals using P-spiro diaminodioxaphosphonium barfates as chiral proton. | |
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MedLine Citation:
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PMID: 20715780 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Chiral diaminodioxaphosphonium salts have been developed and their unique abilities as a chiral proton have been revealed through the establishment of a highly enantioselective protonation of alpha-amino acid-derived ketene disilyl acetals. |
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Authors:
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Daisuke Uraguchi; Natsuko Kinoshita; Takashi Ooi |
Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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Title: Journal of the American Chemical Society Volume: 132 ISSN: 1520-5126 ISO Abbreviation: J. Am. Chem. Soc. Publication Date: 2010 Sep |
Date Detail:
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Created Date: 2010-09-02 Completed Date: 2010-12-23 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 7503056 Medline TA: J Am Chem Soc Country: United States |
Other Details:
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Languages: eng Pagination: 12240-2 Citation Subset: IM |
Affiliation:
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Department of Applied Chemistry, Graduate School of Engineering, Nagoya University, Nagoya 464-8603, Japan. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Acetals
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chemistry* Amino Acids / chemistry* Catalysis Crystallography, X-Ray Esters / chemical synthesis*, chemistry Models, Molecular Molecular Structure Organophosphorus Compounds / chemical synthesis, chemistry* Protons* Silanes / chemistry* |
| Chemical | |
Reg. No./Substance:
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0/Acetals; 0/Amino Acids; 0/Esters; 0/Organophosphorus Compounds; 0/Protons; 0/Silanes |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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