Enantioselective synthesis and conformational analysis of cyclohexene carbocyclic nucleosides

Article abstract of DOI:10.1080/15257779908041505

An enantioselective approach towards the synthesis of optically pure cyclohexene nucleosides 3 has been developed starting from (R)-carvone. The key steps are the regio- and stereoselective hydroboration of an exo double bond, the selective reduction of a

Full text of DOI:10.1080/15257779908041505

This article was downloaded by: [George Mason University]
On: 21 December 2014, At: 16:25
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
Enantioselective Synthesis and
Conformational Analysis of Cyclohexene
Carbocyclic Nucleosides
Jing Wang a & Piet Herdewijn a
a Laboratory of Medicinal Chemistry , Rega Institute for Medical
Research, K. U. Leuven , Minderbroedersstraat 10, B-3000, Leuven,
Belgium
Published online: 04 Oct 2006.
To cite this article: Jing Wang & Piet Herdewijn (1999) Enantioselective Synthesis and Conformational
Analysis of Cyclohexene Carbocyclic Nucleosides, Nucleosides and Nucleotides, 18:4-5, 593-594, DOI:
10.1080/15257779908041505
To link to this article: http://dx.doi.org/10.1080/15257779908041505
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