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  An enzymatic protecting group strategy for the synthesis of nucleopeptides

Jungmann, V., & Waldmann, H. (1998). An enzymatic protecting group strategy for the synthesis of nucleopeptides. TETRAHEDRON LETTERS, 39(10), 1139-1142. doi:10.1016/S0040-4039(97)10873-5.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0014-71B6-2 Version Permalink: http://hdl.handle.net/11858/00-001M-0000-0014-71D7-7
Genre: Journal Article

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 Creators:
Jungmann, V1, Author
Waldmann, Herbert2, Author              
Affiliations:
1external, escidoc:persistent22              
2Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society, escidoc:1753290              

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Free keywords: SOLID-PHASE SYNTHESIS; ADENOVIRUS-2 NUCLEOPROTEIN; L-SERINE; PEPTIDES; HYDROLYSIS; PROTEINS; ESTER
 Abstract: Enzymatic protecting group techniques are used for the selective synthesis of acid-and base labile multifunctional nucleopeptides under mild conditions. (C) 1998 Elsevier Science Ltd. All rights reserved.

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Language(s): eng - English
 Dates: 1998
 Publication Status: Published in print
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Method: Peer
 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: 1139 - 1142 Identifier: ISSN: 0040-4039