Synthesis and antiviral evaluation of 3'-deoxy-β-L-erythro- pentofuranosyl nucleosides of the five naturally occurring nucleic acid bases

Article abstract of DOI:10.1080/15257779508012424

The hitherto unknown title compounds were stereospecifically synthesized by glycosylation of pyrimidine and purine aglycons with a suitably peracylated 3'-deoxy-β-L-erythro-pentofuranose, followed by removal of the protecting groups. All the prepared comp

Full text of DOI:10.1080/15257779508012424

This article was downloaded by: [University North Carolina - Chapel Hill]
On: 01 December 2014, At: 07:53
Publisher: Taylor & Francis
Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered
office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK
Nucleosides and Nucleotides
Publication details, including instructions for authors and
subscription information:
http://www.tandfonline.com/loi/lncn19
Synthesis and Antiviral Evaluation of
3′-Deoxy-β-L-erythro-pentofuranosyl
Nucleosides of the Five Naturally
Occurring Nucleic Acid Bases
C. Mathé a , G. Gosselin a , M.-C. Bergogne a , A.-M. Aubertin b , G.
Obert b , A. Kirn b & J.-L. Imbach a
a Laboratoire de Chimie Bio-Organique, U.R.A. 488 du C.N.R.S. ,
Universitéa Montpellier II , 34095, Montpellier Céadex, 5, France
b Universitéa Louis Pasteur , I.N.S.E.R.M. U 74, 3 Rue Koeberléa,
67000, Strasbourg, France
Published online: 16 Feb 2007.
To cite this article: C. Mathé , G. Gosselin , M.-C. Bergogne , A.-M. Aubertin , G. Obert , A. Kirn
& J.-L. Imbach (1995) Synthesis and Antiviral Evaluation of 3′-Deoxy-β-L-erythro-pentofuranosyl
Nucleosides of the Five Naturally Occurring Nucleic Acid Bases, Nucleosides and Nucleotides, 14:3-5,
549-550
To link to this article: http://dx.doi.org/10.1080/15257779508012424
PLEASE SCROLL DOWN FOR ARTICLE
Taylor & Francis makes every effort to ensure the accuracy of all the information (the
“Content”) contained in the publications on our platform. However, Taylor & Francis,
our agents, and our licensors make no representations or warranties whatsoever as to
the accuracy, completeness, or suitability for any purpose of the Content. Any opinions
and views expressed in this publication are the opinions and views of the authors,
and are not the views of or endorsed by Taylor & Francis. The accuracy of the Content
should not be relied upon and should be independently verified with primary sources
of information. Taylor and Francis shall not be liable for any losses, actions, claims,
proceedings, demands, costs, expenses, damages, and other liabilities whatsoever or
howsoever caused arising directly or indirectly in connection with, in relation to or arising
out of the use of the Content.
This article may be used for research, teaching, and private study purposes. Any
substantial or systematic reproduction, redistribution, reselling, loan, sub-licensing,
systematic supply, or distribution in any form to anyone is expressly forbidden. Terms &

Conditions of access and use can be found at http://www.tandfonline.com/page/terms-
and-conditions