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  SELECTIVE ENZYMATIC REMOVAL OF PROTECTING FUNCTIONS - HEPTYL ESTERS AS CARBOXY PROTECTING GROUPS IN GLYCOPEPTIDE SYNTHESIS

BRAUN, P., Waldmann, H., & KUNZ, H. (1992). SELECTIVE ENZYMATIC REMOVAL OF PROTECTING FUNCTIONS - HEPTYL ESTERS AS CARBOXY PROTECTING GROUPS IN GLYCOPEPTIDE SYNTHESIS. SYNLETT, (1), 39-40.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-9B5D-D Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-9B5F-9
Genre: Journal Article

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 Creators:
BRAUN, P1, Author
Waldmann, Herbert2, Author           
KUNZ, H1, 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: PEPTIDE SYNTHESIS
 Abstract: The selective C-terminal deprotection of acid- and base-labile multifunctional O-glycopeptide heptyl (Hep) esters is achieved under mild conditions (pH 7; 37-degrees-C) by enzymatic hydrolysis with a lipase from Mucor javanicus.

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Language(s): eng - English
 Dates: 1992-01
 Publication Status: Issued
 Pages: 2
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: ISI: A1992HC51600010
 Degree: -

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Title: SYNLETT
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: STUTTGART : GEORG THIEME VERLAG
Pages: - Volume / Issue: (1) Sequence Number: - Start / End Page: 39 - 40 Identifier: ISSN: 0936-5214