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  Chemo-enzymatic synthesis of the C₁₅-C₂₃ unit of leptomycin B

Scheck, M., & Waldmann, H. (2002). Chemo-enzymatic synthesis of the C₁₅-C₂₃ unit of leptomycin B. Canadian Journal of Chemistry - Revue Canadienne de Chimie, 80(6): 1, pp. 571-576. Retrieved from http://article.pubs.nrc-cnrc.gc.ca/ppv/RPViewDoc?_handler_=HandleInitialGet&journal=cjc&volume=80&calyLang=eng&articleFile=v02-070.pdf.

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Genre: Journal Article
Alternative Title : Can. J. Chem. - Rev. Can. Chim.

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 Creators:
Scheck, Michael1, Author
Waldmann, Herbert2, Author           
Affiliations:
1Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753286              
2Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753290              

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Free keywords: leptomycin; natural product synthesis; enzymatic transformation; Aldol reaction; Pseudomonas fluorescence lipase (PFL)
 Abstract: The asymmetric synthesis of the C-15-C-23 unit of Leptomycin B (LMB) is described. All four stereocenters of the C-15-C-23 unit were prepared from one building block exhibiting only one stereocenter. This building block was synthesized via either an enzymatic transformation or starting from a chiral reagent.

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Language(s): eng - English
 Dates: 2002-05-07
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Degree: -

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Title: Canadian Journal of Chemistry - Revue Canadienne de Chimie
  Alternative Title : Can. J. Chem. - Rev. Can. Chim.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 80 (6) Sequence Number: 1 Start / End Page: 571 - 576 Identifier: -