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Nguyen, Bao, Emmett, Edward J., Willis, Michael C. (2010) Palladium-Catalyzed Aminosulfonylation of Aryl Halides. Journal Of The American Chemical Society, 132 (46) 16372-16373 doi:10.1021/ja1081124

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Reference TypeJournal (article/letter/editorial)
TitlePalladium-Catalyzed Aminosulfonylation of Aryl Halides
JournalJournal Of The American Chemical Society
AuthorsNguyen, BaoAuthor
Emmett, Edward J.Author
Willis, Michael C.Author
Year2010 (November 24)Volume132
Issue46
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja1081124Search in ResearchGate
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Mindat Ref. ID1731036Long-form Identifiermindat:1:5:1731036:1
GUID0
Full ReferenceNguyen, Bao, Emmett, Edward J., Willis, Michael C. (2010) Palladium-Catalyzed Aminosulfonylation of Aryl Halides. Journal Of The American Chemical Society, 132 (46) 16372-16373 doi:10.1021/ja1081124
Plain TextNguyen, Bao, Emmett, Edward J., Willis, Michael C. (2010) Palladium-Catalyzed Aminosulfonylation of Aryl Halides. Journal Of The American Chemical Society, 132 (46) 16372-16373 doi:10.1021/ja1081124
In(2010, November) Journal Of The American Chemical Society Vol. 132 (46) American Chemical Society (ACS)

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Emmett, Edward J., Hayter, Barry R., Willis, Michael C. (2014) Palladium-Catalyzed Synthesis of Ammonium Sulfinates from Aryl Halides and a Sulfur Dioxide Surrogate: A Gas- and Reductant-Free Process. Angewandte Chemie, 126 (38). 10368-10372 doi:10.1002/ange.201404527
Emmett, Edward J., Hayter, Barry R., Willis, Michael C. (2014) Palladium-Catalyzed Synthesis of Ammonium Sulfinates from Aryl Halides and a Sulfur Dioxide Surrogate: A Gas- and Reductant-Free Process. Angewandte Chemie International Edition, 53 (38). 10204-10208 doi:10.1002/anie.201404527
Wei, Ming-Kai, Moseley, Daniel F., Bär, Robin M., Sempere, Yeshua, Willis, Michael C. (2024) Palladium-Catalyzed Addition of Aryl Halides to N-Sulfinylamines for the Synthesis of Sulfinamides. Journal of the American Chemical Society, 146 (29) 19690-19695 doi:10.1021/jacs.4c06726
Everson, Daniel A., Shrestha, Ruja, Weix, Daniel J. (2010) Nickel-Catalyzed Reductive Cross-Coupling of Aryl Halides with Alkyl Halides. Journal Of The American Chemical Society, 132 (10) 3636 doi:10.1021/ja100564b
Gandeepan, Parthasarathy, Parthasarathy, Kanniyappan, Cheng, Chien-Hong (2010) Synthesis of Phenanthrone Derivatives fromsec-Alkyl Aryl Ketones and Aryl Halides via a Palladium-Catalyzed Dual C−H Bond Activation and Enolate Cyclization. Journal Of The American Chemical Society, 132 (25) 8569-8571 doi:10.1021/ja1026248
Everson, Daniel A., Shrestha, Ruja, Weix, Daniel J. (2010) Nickel-Catalyzed Reductive Cross-Coupling of Aryl Halides with Alkyl Halides. Journal Of The American Chemical Society, 132 (3) 920-921 doi:10.1021/ja9093956
Trost, Barry M., Czabaniuk, Lara C. (2010) Palladium-Catalyzed Asymmetric Benzylation of 3-Aryl Oxindoles. Journal Of The American Chemical Society, 132 (44) 15534-15536 doi:10.1021/ja1079755
Willis, Michael C. (2007) Palladium-Catalyzed Coupling of Ammonia and Hydroxide with Aryl Halides: The Direct Synthesis of Primary Anilines and Phenols. Angewandte Chemie International Edition, 46 (19). 3402-3404 doi:10.1002/anie.200605071
Wu, Xiao-Feng, Neumann, Helfried, Spannenberg, Anke, Schulz, Thomas, Jiao, Haijun, Beller, Matthias (2010) Development of a General Palladium-Catalyzed Carbonylative Heck Reaction of Aryl Halides. Journal Of The American Chemical Society, 132 (41) 14596-14602 doi:10.1021/ja1059922
Gowrisankar, Saravanan, Sergeev, Alexey G., Anbarasan, Pazhamalai, Spannenberg, Anke, Neumann, Helfried, Beller, Matthias (2010) A General and Efficient Catalyst for Palladium-Catalyzed C−O Coupling Reactions of Aryl Halides with Primary Alcohols. Journal Of The American Chemical Society, 132 (33) 11592-11598 doi:10.1021/ja103248d
de Gombert, Antoine, McKay, Alasdair I., Davis, Christopher J., Wheelhouse, Katherine M., Willis, Michael C. (2020) Mechanistic Studies of the Palladium-Catalyzed Desulfinative Cross-Coupling of Aryl Bromides and (Hetero)Aryl Sulfinate Salts. Journal Of The American Chemical Society, 142 (7) 3564-3576 doi:10.1021/jacs.9b13260
 
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