Nickel-Catalyzed Cross-Coupling of Aryltrimethylammonium Iodides with Organozinc Reagents
Broad scope and good tolerance: An efficient cross‐coupling of aryltrimethylammonium iodide salts with aryl‐, methyl‐, and benzylzinc chlorides catalyzed by [Ni(PCy3)2Cl2] has been achieved (see scheme). The reaction involves cleavage of the CN bond and displays broad substrate scope and good funct...
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Published in | Angewandte Chemie International Edition Vol. 50; no. 21; pp. 4901 - 4904 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
16.05.2011
WILEY‐VCH Verlag Wiley Wiley Subscription Services, Inc |
Edition | International ed. in English |
Subjects | |
Online Access | Get full text |
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Summary: | Broad scope and good tolerance: An efficient cross‐coupling of aryltrimethylammonium iodide salts with aryl‐, methyl‐, and benzylzinc chlorides catalyzed by [Ni(PCy3)2Cl2] has been achieved (see scheme). The reaction involves cleavage of the CN bond and displays broad substrate scope and good functional group tolerance. NMP=N‐methylpyrrolidine. |
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Bibliography: | istex:5593FD19115AECB9F95CD63145BBB1BE32BECE9C ArticleID:ANIE201100683 National Basic Research Program of China - No. 2009CB825300 ark:/67375/WNG-DPCXPKL8-N National Natural Science Foundation of China - No. 20772119 This research was supported by the National Basic Research Program of China (grant no. 2009CB825300) and the National Natural Science Foundation of China (grant no. 20772119). ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201100683 |