An enzymatic protecting group strategy for the synthesis of nucleopeptides

Jungmann, V; Waldmann, Herbert

doi:10.1016/S0040-4039(97)10873-5

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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: https://hdl.handle.net/11858/00-001M-0000-0014-71B6-2 Version Permalink: https://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, ou_persistent22
2Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_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: Date issued: 1998

Publication Status: Issued

Pages: 4

Publishing info: -

Table of Contents: -

Rev. Type: Peer

Identifiers: ISI: 000071994100016
DOI: 10.1016/S0040-4039(97)10873-5

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Title: TETRAHEDRON LETTERS

Source Genre: Journal

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Publ. Info: KIDLINGTON, OXFORD : PERGAMON-ELSEVIER SCIENCE

Pages: - Volume / Issue: 39 (10) Sequence Number: - Start / End Page: 1139 - 1142 Identifier: ISSN: 0040-4039