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AlCl3 mediated unexpected migration of sulfonyl groups: regioselective synthesis of 7-sulfonyl indoles of potential pharmacological interestElectronic supplementary information (ESI) available: Experimental procedures, spectral data for all new compounds, results of docking study. CCDC 859365. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2cc35757g
A conceptually new and straightforward introduction of sulfonyl groups at the C-7 position of an indole ring has been achieved via AlCl 3 mediated unexpected regioselective sulfonyl group migration for N -alkyl/aryl/heteroarylsulfonyl indoles affording potential inhibitors of Mycobacterium tuberculo...
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container_issue | 84 |
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container_volume | 48 |
creator | Prasad, Bagineni Adepu, Raju Sandra, Sandhya Rambabu, D Krishna, G. Rama Reddy, C. Malla Deora, Girdhar Singh Misra, Parimal Pal, Manojit |
description | A conceptually new and straightforward introduction of sulfonyl groups at the C-7 position of an indole ring has been achieved
via
AlCl
3
mediated unexpected regioselective sulfonyl group migration for
N
-alkyl/aryl/heteroarylsulfonyl indoles affording potential inhibitors of
Mycobacterium tuberculosis
H37Rv chorismate mutase.
7-Sulfonyl indoles are synthesized
via
a novel sulfonyl group migration strategy as potential inhibitors of chorismate mutase (CM). |
doi_str_mv | 10.1039/c2cc35757g |
format | article |
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via
AlCl
3
mediated unexpected regioselective sulfonyl group migration for
N
-alkyl/aryl/heteroarylsulfonyl indoles affording potential inhibitors of
Mycobacterium tuberculosis
H37Rv chorismate mutase.
7-Sulfonyl indoles are synthesized
via
a novel sulfonyl group migration strategy as potential inhibitors of chorismate mutase (CM).</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/c2cc35757g</identifier><language>eng</language><creationdate>2012-09</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Prasad, Bagineni</creatorcontrib><creatorcontrib>Adepu, Raju</creatorcontrib><creatorcontrib>Sandra, Sandhya</creatorcontrib><creatorcontrib>Rambabu, D</creatorcontrib><creatorcontrib>Krishna, G. Rama</creatorcontrib><creatorcontrib>Reddy, C. Malla</creatorcontrib><creatorcontrib>Deora, Girdhar Singh</creatorcontrib><creatorcontrib>Misra, Parimal</creatorcontrib><creatorcontrib>Pal, Manojit</creatorcontrib><title>AlCl3 mediated unexpected migration of sulfonyl groups: regioselective synthesis of 7-sulfonyl indoles of potential pharmacological interestElectronic supplementary information (ESI) available: Experimental procedures, spectral data for all new compounds, results of docking study. CCDC 859365. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2cc35757g</title><description>A conceptually new and straightforward introduction of sulfonyl groups at the C-7 position of an indole ring has been achieved
via
AlCl
3
mediated unexpected regioselective sulfonyl group migration for
N
-alkyl/aryl/heteroarylsulfonyl indoles affording potential inhibitors of
Mycobacterium tuberculosis
H37Rv chorismate mutase.
7-Sulfonyl indoles are synthesized
via
a novel sulfonyl group migration strategy as potential inhibitors of chorismate mutase (CM).</description><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFkT1PwzAQhgMCCSgs7EjHBhItLWn6taE0FZ0YYGCrjH1JDY5t2U4hf4DfzSUgOiCBF5_Oz7333jmKTgf93qAfT6_5DedxMk7GxW50OIhHw24ynDztNXEy7Y7jYXIQHXn_0qczSCaHOx-3KlUxlCgkCyig0vhukTdhKQvHgjQaTA6-UrnRtYLCmcr6GTgspPGoiJUbBF_rsEYvfQOPuz-41MIobLPWBNRBMgV2zVzJuFGmkJw1UECHPmSNmjNacupnrcKSCpirCcgNVbRmLrKH5SWwDZOKPSucQUaGnWxRknaGo6hI7Qp8M4ijpGCBASkAUwo0vgE3pTWVFgQRWanQGhSGv0pdgA-VqHuQpvMUJsk0HiU9WFA1NQamBXBXe-pF7h2zazLb6ksN6XIBxBnahAPcDvNlHjwizO-XM_j9W8fRfs6Ux5PvuxOdLbLH9K7rPF9Zmo62sNricSc6_-t9ZUUe_6fxCcxguvQ</recordid><startdate>20120926</startdate><enddate>20120926</enddate><creator>Prasad, Bagineni</creator><creator>Adepu, Raju</creator><creator>Sandra, Sandhya</creator><creator>Rambabu, D</creator><creator>Krishna, G. Rama</creator><creator>Reddy, C. Malla</creator><creator>Deora, Girdhar Singh</creator><creator>Misra, Parimal</creator><creator>Pal, Manojit</creator><scope/></search><sort><creationdate>20120926</creationdate><title>AlCl3 mediated unexpected migration of sulfonyl groups: regioselective synthesis of 7-sulfonyl indoles of potential pharmacological interestElectronic supplementary information (ESI) available: Experimental procedures, spectral data for all new compounds, results of docking study. CCDC 859365. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2cc35757g</title><author>Prasad, Bagineni ; Adepu, Raju ; Sandra, Sandhya ; Rambabu, D ; Krishna, G. Rama ; Reddy, C. Malla ; Deora, Girdhar Singh ; Misra, Parimal ; Pal, Manojit</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c2cc35757g3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prasad, Bagineni</creatorcontrib><creatorcontrib>Adepu, Raju</creatorcontrib><creatorcontrib>Sandra, Sandhya</creatorcontrib><creatorcontrib>Rambabu, D</creatorcontrib><creatorcontrib>Krishna, G. Rama</creatorcontrib><creatorcontrib>Reddy, C. Malla</creatorcontrib><creatorcontrib>Deora, Girdhar Singh</creatorcontrib><creatorcontrib>Misra, Parimal</creatorcontrib><creatorcontrib>Pal, Manojit</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Prasad, Bagineni</au><au>Adepu, Raju</au><au>Sandra, Sandhya</au><au>Rambabu, D</au><au>Krishna, G. Rama</au><au>Reddy, C. Malla</au><au>Deora, Girdhar Singh</au><au>Misra, Parimal</au><au>Pal, Manojit</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>AlCl3 mediated unexpected migration of sulfonyl groups: regioselective synthesis of 7-sulfonyl indoles of potential pharmacological interestElectronic supplementary information (ESI) available: Experimental procedures, spectral data for all new compounds, results of docking study. CCDC 859365. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2cc35757g</atitle><date>2012-09-26</date><risdate>2012</risdate><volume>48</volume><issue>84</issue><spage>1434</spage><epage>1436</epage><pages>1434-1436</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>A conceptually new and straightforward introduction of sulfonyl groups at the C-7 position of an indole ring has been achieved
via
AlCl
3
mediated unexpected regioselective sulfonyl group migration for
N
-alkyl/aryl/heteroarylsulfonyl indoles affording potential inhibitors of
Mycobacterium tuberculosis
H37Rv chorismate mutase.
7-Sulfonyl indoles are synthesized
via
a novel sulfonyl group migration strategy as potential inhibitors of chorismate mutase (CM).</abstract><doi>10.1039/c2cc35757g</doi><tpages>3</tpages></addata></record> |
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source | Royal Society of Chemistry Journals |
title | AlCl3 mediated unexpected migration of sulfonyl groups: regioselective synthesis of 7-sulfonyl indoles of potential pharmacological interestElectronic supplementary information (ESI) available: Experimental procedures, spectral data for all new compounds, results of docking study. CCDC 859365. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2cc35757g |
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