C-nucleoside analogues of nicotinamide mononucleotide (NMN) Conference Paper

  


Authors: Pankiewicz, K.; Kabat, M. M.; Sochacka, E.; Ciszewski, L.; Zeidler, J.; Watanabe, K. A.
Title: C-nucleoside analogues of nicotinamide mononucleotide (NMN)
Conference Title: 2nd Swedish-German Workshop on Modern Aspects of Chemistry and Biochemistry of Nucleic Acids and their Components
Abstract: 5-(β-D-Ribofuranosyl)nicotinamide (IIc) and 6-(β-D-ribo-furanosyl) picolinamide (lid) and their corresponding α-isomers (III) were synthesized from ribonolactone. The C-nucleoside IIc was further converted to its 5′-monophosphate IIp which is isosteric to NMN (Ip). © 1988, Taylor & Francis Group, LLC. All rights reserved.
Journal Title Nucleosides & Nucleotides
Volume: 7
Issue: 5-6
Conference Dates: 1988 Mar 24-27
Conference Location: Ulm, West Germany
ISBN: 0732-8311
Publisher: Taylor & Francis Inc.  
Date Published: 1988-10-01
Start Page: 589
End Page: 593
Language: English
DOI: 10.1080/07328318808056291
PROVIDER: scopus
DOI/URL:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-3142767228&doi=10.1080%2f07328318808056291&partnerID=40&md5=43fa3e2d59226e1e0ed1ded80e082b61
Notes: Article -- Export Date: 6 August 2020 -- Source: Scopus
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MSK Authors
  1. Kyoichi A Watanabe
    125 Watanabe
  2. Krzystof W. Pankiewicz
    43 Pankiewicz
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