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  A short enantioselective synthesis of 1-deoxy-L-xylulose by antibody catalysis

Shabat, D., List, B., Lerner, R. A., & Barbas III, C. F. (1999). A short enantioselective synthesis of 1-deoxy-L-xylulose by antibody catalysis. Tetrahedron Letters, 40(8), 1437-1440. doi:10.1016/S0040-4039(98)02699-9.

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 Creators:
Shabat, Doron1, Author
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: A new efficient synthesis of 1-deoxy-l-xylulose (1) is presented. The key step is achieved by a highly enantioselective aldol addition of hydroxyacetone to benzyloxyacetaldehyde via antibody catalysis. The synthesis described here should provide a convenient route to isotopically labeled derivatives.

A two step enantioselective synthesis of 1-deoxy-L-xylulose has been achieved utilizing aldolase antibody 38C2 (Aldrich #47,995-0)

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Language(s): eng - English
 Dates: 1998-10-301999-02-19
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/S0040-4039(98)02699-9
 Degree: -

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Title: Tetrahedron Letters
  Abbreviation : Tetrahedron Lett.
Source Genre: Journal
 Creator(s):
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Publ. Info: Oxford : Pergamon
Pages: - Volume / Issue: 40 (8) Sequence Number: - Start / End Page: 1437 - 1440 Identifier: ISSN: 0040-4039
CoNE: https://pure.mpg.de/cone/journals/resource/954925448772