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  Synthesis of characteristic lipopeptides of lipid modified proteins employing the allyl ester as protecting group

Schmittberger, T., Cotte, A., & Waldmann, H. (1998). Synthesis of characteristic lipopeptides of lipid modified proteins employing the allyl ester as protecting group. CHEMICAL COMMUNICATIONS, (8), 937-938. doi:10.1039/a708749g.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-71B2-A Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-71D9-3
Genre: Journal Article

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 Creators:
Schmittberger, T1, Author
Cotte, A1, 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: RAS Chemistry
 Abstract: Lipidated peptides which represent characteristic lipid modified substructures of lipidated human G(alpha O) protein and the human N- and R-Ras proteins were built up efficiently by employing the selective Pd-0-mediated removal of allyl esters under very mild conditions as the key step.

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Language(s): eng - English
 Dates: 1998
 Publication Status: Issued
 Pages: 2
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: ISI: 000073297800040
DOI: 10.1039/a708749g
 Degree: -

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Title: CHEMICAL COMMUNICATIONS
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: CAMBRIDGE UK : ROYAL SOC CHEMISTRY
Pages: - Volume / Issue: (8) Sequence Number: - Start / End Page: 937 - 938 Identifier: ISSN: 1359-7345