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Palladium-Catalyzed Cross-Coupling of α-Diazocarbonyl Compounds with Arylboronic Acids
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Abstract
Pd(PPh3)4-catalyzed reaction between α−diazocarbonyl compounds and arylboronic acids leads to the formation of cross-coupling products in good yields.
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This article has been cited by 14 ACS Journal articles (5 most recent appear below).
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Well-Defined Binuclear Chiral Spiro Copper Catalysts for Enantioselective N–H Insertion
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Pd-Catalyzed Carbonylation of Diazo Compounds at Atmospheric Pressure: A Catalytic Approach to Ketenes
Zhenhua Zhang, Yiyang Liu, Lin Ling, Yuxue Li, Yian Dong, Mingxing Gong, Xiaokun Zhao, Yan Zhang, and Jianbo WangJournal of the American Chemical Society2011 133 (12), 4330-4341Pd-Catalyzed Carbonylation of Diazo Compounds at Atmospheric Pressure: A Catalytic Approach to Ketenes
Zhenhua Zhang, Yiyang Liu, Lin Ling, Yuxue Li, Yian Dong, Mingxing Gong, Xiaokun Zhao, Yan Zhang, and Jianbo WangJournal of the American Chemical Society2011 133 (12), 4330-4341The carbonylation of carbenes through catalytic cycles is highly desirable due to the importance of ketene-mediated reactions in organic synthesis. In this investigation, a highly efficient and mild catalytic approach toward ketene intermediates has been ...
Transmetalation of Unsaturated Carbon Nucleophiles from Boron-Containing Species to the Mid to Late d-Block Metals of Relevance to Catalytic C−X Coupling Reactions (X = C, F, N, O, Pb, S, Se, Te)
David V. PartykaChemical Reviews2011 111 (3), 1529-1595Transmetalation of Unsaturated Carbon Nucleophiles from Boron-Containing Species to the Mid to Late d-Block Metals of Relevance to Catalytic C−X Coupling Reactions (X = C, F, N, O, Pb, S, Se, Te)
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Catalytic Thia-Sommelet−Hauser Rearrangement: Application to the Synthesis of Oxindoles
Yuye Li, Yi Shi, Zhongxing Huang, Xinhu Wu, Pengfei Xu, Jianbo Wang, and Yan ZhangOrganic Letters2011 13 (5), 1210-1213Catalytic Thia-Sommelet−Hauser Rearrangement: Application to the Synthesis of Oxindoles
Yuye Li, Yi Shi, Zhongxing Huang, Xinhu Wu, Pengfei Xu, Jianbo Wang, and Yan ZhangOrganic Letters2011 13 (5), 1210-1213A series of 3-arylthio-1,3-disubstituted-oxindoles were prepared in good yields by the reaction of α-diazocarbonyl compounds and sulfenamides. The reaction involves a Rh-catalyzed thia-Sommelet−Hauser-type rearrangement.
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History
- Published In Issue February 06, 2008
- Received October 27, 2007
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