A concise and stereoselective synthesis of C-glycosyl analogues of β-L-fucopyranosyl phosphate and β-L-rhamnopyranosyl phosphate

Article abstract of DOI:10.1080/07328309908544057

The isosteric C-glycosyl analogues of β-L-fucopyranosyl phosphate 1 and β-L-rhamnopyranosyl phosphate 2 have been stereoselectively synthesized from the corresponding glycono-1,5-lactones 3 and 10 via methylphosphonylation, dehydration and catalytic hydro

Full text of DOI:10.1080/07328309908544057

This article was downloaded by: [Oklahoma State University]
On: 20 December 2014, At: 21:32
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
Journal of Carbohydrate Chemistry
Publication details, including instructions for authors and
subscription information:
http://www.tandfonline.com/loi/lcar20
A Concise and Stereoselective
Synthesis of C-Glycosyl Analogues of
β-L-Fucopyranosyl Phosphate and β-
L-Rhamnopyranosyl Phosphate
Andrew J. Norris & Tatsushi Toyokuni
a Crump Institute for Biological Imaging, Department
of Molecular & Medical Pharmacology, UCLA School of
Medicine , Los Angeles, California 90095-1770, U.S.A.
b Crump Institute for Biological Imaging, Department
of Molecular & Medical Pharmacology, UCLA School of
Medicine , Los Angeles, California 90095-1770, U.S.A.
Published online: 27 Feb 2008.
To cite this article: Andrew J. Norris & Tatsushi Toyokuni (1999) A Concise and
Stereoselective Synthesis of C-Glycosyl Analogues of β-L-Fucopyranosyl Phosphate and β-
L-Rhamnopyranosyl Phosphate, Journal of Carbohydrate Chemistry, 18:9, 1097-1105, DOI:
10.1080/07328309908544057
To link to this article: http://dx.doi.org/10.1080/07328309908544057
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