An Efficient Synthesis of a New Series of Acyclonucleosides Starting from β-Amino Alcohols
Author:
Affiliation:
1. Laboratoire de Synthèse Asymétrique (UMR CNRS 7611), Case courrier 47, Université P. et M. Curie, 4 place Jussieu, 75005 Paris, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo000812d
Reference24 articles.
1. 9-(2-Hydroxyethoxymethyl)guanine activity against viruses of the herpes group
2. 5-fluorouracil derivatives. 1. Acyclonucleosides through a tin (IV) chloride-mediated regiospecific ring opening of alkoxy-1,4-diheteroepanes
3. Chemical modifications on the acyclic moiety of 3-(2-hydroxyethoxy)-1-alkoxypropyl nucleobases. 2. Differentiation and growth inhibition in rhabdomyosarcoma cells after exposure to a novel 5-fluorouracil acyclonucleoside
4. Chemistry and antiviral activities of acyclonucleosides
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