Rhodium-Catalyzed Regioselective C–H Chlorination of 7‑Azaindoles Using 1,2-Dichloroethane
An unexpected rhodium-catalyzed regioselective C–H chlorination of 7-azaindoles was developed using 1,2-dichloroethane (DCE) as a chlorinating agent and 7-azaindole as the directing group. This protocol provides an efficient access to ortho-chlorinated azaindoles with operational simplicity, good fu...
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| Published in | Organic letters Vol. 16; no. 20; pp. 5294 - 5297 |
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| Main Authors | , , , , |
| Format | Journal Article |
| Language | English |
| Published |
WASHINGTON
American Chemical Society
17.10.2014
Amer Chemical Soc |
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| Online Access | Get full text |
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| Abstract | An unexpected rhodium-catalyzed regioselective C–H chlorination of 7-azaindoles was developed using 1,2-dichloroethane (DCE) as a chlorinating agent and 7-azaindole as the directing group. This protocol provides an efficient access to ortho-chlorinated azaindoles with operational simplicity, good functional group tolerance, and a wide substrate scope. |
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| AbstractList | An unexpected rhodium-catalyzed regioselective C–H chlorination of 7-azaindoles was developed using 1,2-dichloroethane (DCE) as a chlorinating agent and 7-azaindole as the directing group. This protocol provides an efficient access to ortho-chlorinated azaindoles with operational simplicity, good functional group tolerance, and a wide substrate scope. |
| Author | Xu, Bin Hong, Xiaohu Mao, Hong Liu, Bingxin Qian, Guangyin |
| AuthorAffiliation | Chinese Academy of Sciences Shanghai University East China Normal University State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry Department of Chemistry, Innovative Drug Research Center Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Department of Chemistry |
| AuthorAffiliation_xml | – name: State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry – name: East China Normal University – name: Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Department of Chemistry – name: Shanghai University – name: Chinese Academy of Sciences – name: Department of Chemistry, Innovative Drug Research Center |
| Author_xml | – sequence: 1 givenname: Guangyin surname: Qian fullname: Qian, Guangyin – sequence: 2 givenname: Xiaohu surname: Hong fullname: Hong, Xiaohu – sequence: 3 givenname: Bingxin surname: Liu fullname: Liu, Bingxin email: bxliu@shu.edu.cn – sequence: 4 givenname: Hong surname: Mao fullname: Mao, Hong – sequence: 5 givenname: Bin surname: Xu fullname: Xu, Bin email: xubin@shu.edu.cn |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25251224$$D View this record in MEDLINE/PubMed |
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| Copyright | Copyright © 2014 American Chemical Society |
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| Keywords | FUNCTIONALIZATION RECEPTOR ANTAGONISTS ARYLATION ISOCYANIDES CYANATION OXIDATIVE ANNULATION BONDS EFFICIENT ACCESS HALOGENATION ALKYNES SP |
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| Snippet | An unexpected rhodium-catalyzed regioselective C–H chlorination of 7-azaindoles was developed using 1,2-dichloroethane (DCE) as a chlorinating agent and... An unexpected rhodium-catalyzed regioselective C-H chlorination of 7-azaindoles was developed using 1,2-dichloroethane (DCE) as a chlorinating agent and... |
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| SubjectTerms | Chemistry Chemistry, Organic Physical Sciences Science & Technology |
| Title | Rhodium-Catalyzed Regioselective C–H Chlorination of 7‑Azaindoles Using 1,2-Dichloroethane |
| URI | http://dx.doi.org/10.1021/ol502447w http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000343526200017 https://www.ncbi.nlm.nih.gov/pubmed/25251224 https://search.proquest.com/docview/1613941307 |
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