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  Enantioselective Aldol Cyclodehydrations Catalyzed by Antibody 38C2

List, B., Lerner, R. A., & Barbas III, C. F. (1999). Enantioselective Aldol Cyclodehydrations Catalyzed by Antibody 38C2. Organic Letters, 1(1), 59-62. doi:10.1021/ol9905405.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-A4F0-B Version Permalink: https://hdl.handle.net/21.11116/0000-0008-38C4-C
Genre: Journal Article

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 Creators:
List, Benjamin1, Author           
Lerner, Richard A.1, Author
Barbas III, Carlos F.1, Author
Affiliations:
1The Skaggs Institute for Chemical Biology and the 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: Aldolase antibody 38C2 catalyzes the enantioselective aldol cyclodehydration of 4-substituted-2,6-heptanediones (3) to give enantiomerically enriched 5-substituted-3-methyl-2-cyclohexen-1-ones (4). Yields, enantioselectivities, and product purities are markedly increased compared to the l-proline-catalyzed reactions.

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Language(s): eng - English
 Dates: 1999-03-261999-07-01
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/ol9905405
 Degree: -

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Title: Organic Letters
  Abbreviation : Org. Lett.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 1 (1) Sequence Number: - Start / End Page: 59 - 62 Identifier: ISSN: 1523-7060
CoNE: https://pure.mpg.de/cone/journals/resource/954925626338