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  Efficient enantioselective synthesis of a beta-hydroxyepoxide building block for the construction of macrocyclic natural products

Schlede, U., Nazare, M., & Waldmann, H. (1998). Efficient enantioselective synthesis of a beta-hydroxyepoxide building block for the construction of macrocyclic natural products. TETRAHEDRON LETTERS, 39(10), 1143-1144. doi:10.1016/S0040-4039(97)10874-7.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-71B8-D Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-71D6-9
Genre: Journal Article

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 Creators:
Schlede, U1, Author
Nazare, M1, Author
Waldmann, Herbert2, Author           
Affiliations:
1external, ou_persistent22              
2Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753290              

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Free keywords: POLYENE MACROLIDE ANTIBIOTICS; METABOLITES
 Abstract: The synthesis of a protected beta-hydroxyepoxide macrolide building block in seven steps from commercially available (R)-3-hydroxybutyric acid methyl ester in 68% overall yield is described. (C) 1998 Elsevier Science Ltd. All rights reserved.

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Language(s): eng - English
 Dates: 1998
 Publication Status: Issued
 Pages: 2
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: ISI: 000071994100017
DOI: 10.1016/S0040-4039(97)10874-7
 Degree: -

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Title: TETRAHEDRON LETTERS
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: KIDLINGTON, OXFORD : PERGAMON-ELSEVIER SCIENCE
Pages: - Volume / Issue: 39 (10) Sequence Number: - Start / End Page: 1143 - 1144 Identifier: ISSN: 0040-4039