A straightforward entry to chiral carbocyclic nucleoside analogues via the enantioselective [3+2] cycloaddition of α-nucleobase substituted acrylates1. Issue 62 (11th August 2015)

Record Type:: Journal Article
Title:: A straightforward entry to chiral carbocyclic nucleoside analogues via the enantioselective [3+2] cycloaddition of α-nucleobase substituted acrylates1. Issue 62 (11th August 2015)
Main Title:: A straightforward entry to chiral carbocyclic nucleoside analogues via the enantioselective [3+2] cycloaddition of α-nucleobase substituted acrylates1
Authors:: Xie, Ming-Sheng
Wang, Yong
Li, Jian-Ping
Du, Cong
Zhang, Yan-Yan
Hao, Er-Jun
Zhang, Yi-Ming
Qu, Gui-Rong
Guo, Hai-Ming
Abstract:: <abstract abstract-type="toc"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <graphic position="anchor" id="ga" xlink:href="ark:/27927/pgj2b31nwwr" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" />A straightforward entry to chiral carbocyclic nucleoside analogues is achieved <italic>via</italic> the enantioselective [3+2] cycloaddition of α-nucleobase substituted acrylates to vinyl cyclopropanes.</p> </abstract>
Is Part Of:: Chemical communications. Volume 51:Issue 62(2015)
Journal:: Chemical communications
Issue:: Volume 51:Issue 62(2015)
Issue Display:: Volume 51, Issue 62 (2015)
Year:: 2015
Volume:: 51
Issue:: 62
Issue Sort Value:: 2015-0051-0062-0000
Page Start:: 12451
Page End:: 12454
Publication Date:: 2015-08-11
Subjects:: Chemistry -- Periodicals
540
Journal URLs:: http://pubs.rsc.org/en/journals/journalissues/cc ↗
http://www.rsc.org/ ↗
DOI:: 10.1039/c5cc04832j ↗
Languages:: English
ISSNs:: 1359-7345
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3139.350000
British Library DSC - BLDSS-3PM
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Ingest File:: 3448.xml