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Mendeleev Communications, 2015,
Volume 25
,
Issue 2
,
Pages
121–123
DOI:
https://doi.org/10.1016/j.mencom.2015.03.014
(Mi mendc2320)
This article is cited in
2
scientific papers (total in
2
papers)
Communications
New cycloheptane nucleoside analogues
A. I. Tsybin
,
V. P. Perevalov
D.Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation
Full-text PDF (420 kB)
Citations (2)
Supplementary materials
DOI:
https://doi.org/10.1016/j.mencom.2015.03.014
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Abstract:
Epoxidation of 1-phenylcyclohept-4-ene-1-carbonitrile gives mostly
E
-isomer of the desired epoxy derivative, whose ring opening with adenine or thymine proceeds stereoselectively providing access to novel cycloheptane nucleoside analogues.
Bibliographic databases:
Document Type:
Article
Language:
English
Supplementary materials:
Supplementary_data_1.pdf
(503.3 Kb)
Citation:
A. I. Tsybin, V. P. Perevalov, “New cycloheptane nucleoside analogues”,
Mendeleev Commun.
,
25
:2 (2015),
121–123
Linking options:
https://www.mathnet.ru/eng/mendc2320
https://www.mathnet.ru/eng/mendc/v25/i2/p121
This publication is cited in the following 2 articles:
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