Stereoselective synthesis of β-L-2',3'- dideoxy- and L-2',3'- didehydro-2',3'-dideoxy purine nucleosides

Article abstract of DOI:10.1080/07328319908044642

β-L-2',3'-Dideoxy- and L-2',Y-didehydro-2',Y-dideoxy purine nucleosides have been synthesized via a highly stereoselective method of glycosylation by the condensation of L-2-(phenylselenyl)-2,3-dideoxyribose derivative with silylated heterocyclic base.

Full text of DOI:10.1080/07328319908044642

This article was downloaded by: [Temple University Libraries]
On: 23 November 2014, At: 14:24
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
Stereoselective Synthesis of β-L-2′, 3′-
Dideoxy-and L-2′,3′-Didehydro-2′,3′-
Dideoxy Purine Nucleosides
Peiyuan Wang a , Pascal J. Bolon a , M. Gary Newton b & Chung K.
Chua a
a Department of Pharmaceutical and Biomedical Sciences , College
of Pharmacy , Athens, Georgia , 30602
b Department of Chemistry , The University of Georgia , Athens,
Georgia , 30602
Published online: 04 Oct 2006.
To cite this article: Peiyuan Wang , Pascal J. Bolon , M. Gary Newton & Chung K. Chua (1999)
Stereoselective Synthesis of β-L-2′, 3′-Dideoxy-and L-2′,3′-Didehydro-2′,3′-Dideoxy Purine
Nucleosides, Nucleosides and Nucleotides, 18:11-12, 2819-2835, DOI: 10.1080/07328319908044642
To link to this article: http://dx.doi.org/10.1080/07328319908044642
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