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01735 am a22003613u 4500 |
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99484 |
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|a Fors, Brett P.
|e author
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|a Massachusetts Institute of Technology. Department of Chemistry
|e contributor
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|a Fors, Brett P.
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|a Dooleweerdt, Karin
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|a Zeng, Qingle
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|a Buchwald, Stephen Leffler
|e contributor
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|a Dooleweerdt, Karin
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|a Zeng, Qingle
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|a Buchwald, Stephen Leffler
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|a An efficient system for the Pd-catalyzed cross-coupling of amides and aryl chlorides
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|b Elsevier,
|c 2015-10-28T12:51:22Z.
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| 856 |
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|z Get fulltext
|u http://hdl.handle.net/1721.1/99484
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|a A catalyst based on a new biarylphosphine ligand (3) for the Pd-catalyzed cross-coupling reactions of amides and aryl chlorides is described. This system shows the highest turnover frequencies reported to date for these reactions, especially for aryl chloride substrates bearing an ortho substituent. An array of amides and aryl chlorides were successfully reacted in good to excellent yields.
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|a National Institutes of Health (U.S.) (Grant GM-58160)
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|a Merck & Co., Inc.
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|a BASF
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|a Chemetall
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|a Nippon Chemical Industrial Co.
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|a William Asbornsen Albert Memorial Fund (Fellowship)
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|a University of Aarhus. Department of Chemistry
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|a University of Aarhus. Interdisciplinary Nanoscience Centre
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|a China Scholarship Council
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|a National Natural Science Foundation (China) (Grant 20672088)
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|a en_US
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|a Article
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|t Tetrahedron
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