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  Synthese 5′-substituierter Adenosinderivate

Jahn, W. (1965). Synthese 5′-substituierter Adenosinderivate. Chemische Berichte, 98(6), 1705-1708. doi:10.1002/cber.19650980604.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-002D-3B62-0 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-002D-3B63-E
Genre: Journal Article

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ChemBerichte_98_1965_1705.pdf (Any fulltext), 241KB
 
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http://onlinelibrary.wiley.com/doi/10.1002/cber.19650980604/epdf (Any fulltext)
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 Creators:
Jahn, Werner1, Author           
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1Emeritus Group Biophysics, Max Planck Institute for Medical Research, Max Planck Society, ou_1497712              

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 Abstract: Die bei nucleophilen Substitutionen störende Umlagerung des 5′-O-Tosyl-2′.3′-O-isopropyliden-adenosins zu einem „Cyclo-nucleosid-Salz” läßt sich durch N-Acylierung vermeiden. Damit werden verschiedene bisher nicht durchführbare Austauschreaktionen möglich.

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Language(s): deu - German
 Dates: 1964-10-052006-01-211965-06
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/cber.19650980604
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Title: Chemische Berichte
  Other : Chem. Ber.
Source Genre: Journal
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Publ. Info: Weinheim : VCH Verlagsgesellschaft mbH
Pages: - Volume / Issue: 98 (6) Sequence Number: - Start / End Page: 1705 - 1708 Identifier: ISSN: 0009-2940
CoNE: https://pure.mpg.de/cone/journals/resource/954926940716