Manganese catalyzed C–H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity1. Issue 33 (28th April 2015)

Record Type:: Journal Article
Title:: Manganese catalyzed C–H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity1. Issue 33 (28th April 2015)
Main Title:: Manganese catalyzed C–H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity1
Authors:: Shi, Lijun
Zhong, Xiang
She, Houde
Lei, Ziqiang
Li, Fuwei
Abstract:: <abstract abstract-type="toc"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <graphic position="anchor" id="ga" xlink:href="ark:/27927/pgjn2dsjvv" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" />The Mn-catalyzed C–H alkenylations of indole with terminal- and/or internal-alkynes have been developed to selectively yield indolylalkene and carbazole.</p> </abstract>
Is Part Of:: Chemical communications. Volume 51:Issue 33(2015)
Journal:: Chemical communications
Issue:: Volume 51:Issue 33(2015)
Issue Display:: Volume 51, Issue 33 (2015)
Year:: 2015
Volume:: 51
Issue:: 33
Issue Sort Value:: 2015-0051-0033-0000
Page Start:: 7136
Page End:: 7139
Publication Date:: 2015-04-28
Subjects:: Chemistry -- Periodicals
540
Journal URLs:: http://pubs.rsc.org/en/journals/journalissues/cc ↗
http://www.rsc.org/ ↗
DOI:: 10.1039/c5cc00249d ↗
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:: 3158.xml