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  Quantum Mechanical Predictions of the Stereoselectivities of Proline-Catalyzed Asymmetric Intermolecular Aldol Reactions

Bahmanyar, S., Houk, K. N., Martin, H. J., & List, B. (2003). Quantum Mechanical Predictions of the Stereoselectivities of Proline-Catalyzed Asymmetric Intermolecular Aldol Reactions. Journal of the American Chemical Society, 125(9), 2475-2479. doi:10.1021/ja028812d.

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 Creators:
Bahmanyar, S.1, Author
Houk, K. N. 1, Author
Martin, Harry J.2, Author
List, Benjamin2, Author           
Affiliations:
1Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569, ou_1445585              
2The Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA., ou_persistent22              

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 Abstract: Quantum mechanical calculations were employed to predict the ratio of four stereoisomeric products expected from two complex reactions involving the aldol reactions of cyclohexanone with benzaldehyde or with isobutyraldehyde catalyzed by (S)-proline. Experimental tests of these predictions provide an assessment of the state-of-the-art in quantum mechanical prediction of products of complex organic reactions in solution.

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Language(s): eng - English
 Dates: 2002-10-042003-02-082003-03-01
 Publication Status: Issued
 Pages: 5
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/ja028812d
 Degree: -

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Title: Journal of the American Chemical Society
  Other : JACS
  Abbreviation : J. Am. Chem. Soc.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 125 (9) Sequence Number: - Start / End Page: 2475 - 2479 Identifier: ISSN: 0002-7863
CoNE: https://pure.mpg.de/cone/journals/resource/954925376870