Novel synthesis of (+/-)-cis-4-amino-2-cyclopentene-1-methanol, a key intermediate in the preparation of carbocyclic 2',3'-didehydro-2',3'-dideoxy nucleosides

Article abstract of DOI:10.1080/00397919208021133

Novel synthetic routes directed toward the preparation of (+/-)-cis-4-amino-2-cyclopentene-1-methanol are described. The routes investigated involve azide openings of chiral and non-chiral cyclopentyl epoxides.

Full text of DOI:10.1080/00397919208021133

This article was downloaded by: [University of Auckland Library]
On: 07 December 2014, At: 13:26
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
Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
Publication details, including instructions for
authors and subscription information:
http://www.tandfonline.com/loi/lsyc20
Novel Synthesis of (+/-)-cis-4-
Amino-2-cyclopentene-1-
methanol, a Key Intermediate
in the Preparation
of Carbocyclic 2′,3′-
Didehydro-2′,3′-dideoxy
Nucleosides
Mark H. Norman a , Merrick R. Almond a , Barbara E.
Reitter a & S. George Rahim b
a Division of Organic Chemistry , Burroughs
Wellcome Co. , Research Triangle Park, NC, 27709
b Medicinal Chemistry Department , Wellcome
Research Laboratories Beckenham , Kent, England ,
BR3 3BS
Published online: 23 Sep 2006.
To cite this article: Mark H. Norman , Merrick R. Almond , Barbara E. Reitter &
S. George Rahim (1992) Novel Synthesis of (+/-)-cis-4-Amino-2-cyclopentene-1-
methanol, a Key Intermediate in the Preparation of Carbocyclic 2′,3′-
Didehydro-2′,3′-dideoxy Nucleosides, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 22:22, 3197-3204,
DOI: 10.1080/00397919208021133
To link to this article: http://dx.doi.org/10.1080/00397919208021133

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