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Stambuli, James P., Kuwano, Ryoichi, Hartwig, John F. (2002) Unparalleled Rates for the Activation of Aryl Chlorides and Bromides: Coupling with Amines and Boronic Acids in Minutes at Room Temperature. Angewandte Chemie, 114 (24). 4940-4942 doi:10.1002/ange.200290035

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Reference TypeJournal (article/letter/editorial)
TitleUnparalleled Rates for the Activation of Aryl Chlorides and Bromides: Coupling with Amines and Boronic Acids in Minutes at Room Temperature
JournalAngewandte Chemie
AuthorsStambuli, James P.Author
Kuwano, RyoichiAuthor
Hartwig, John F.Author
Year2002 (December 16)Volume114
Issue24
PublisherWiley
DOIdoi:10.1002/ange.200290035Search in ResearchGate
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Mindat Ref. ID7299075Long-form Identifiermindat:1:5:7299075:9
GUID0
Full ReferenceStambuli, James P., Kuwano, Ryoichi, Hartwig, John F. (2002) Unparalleled Rates for the Activation of Aryl Chlorides and Bromides: Coupling with Amines and Boronic Acids in Minutes at Room Temperature. Angewandte Chemie, 114 (24). 4940-4942 doi:10.1002/ange.200290035
Plain TextStambuli, James P., Kuwano, Ryoichi, Hartwig, John F. (2002) Unparalleled Rates for the Activation of Aryl Chlorides and Bromides: Coupling with Amines and Boronic Acids in Minutes at Room Temperature. Angewandte Chemie, 114 (24). 4940-4942 doi:10.1002/ange.200290035
In(2002, December) Angewandte Chemie Vol. 114 (24) Wiley

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Stambuli, James P., Kuwano, Ryoichi, Hartwig, John F. (2002) Unparalleled Rates for the Activation of Aryl Chlorides and Bromides: Coupling with Amines and Boronic Acids in Minutes at Room Temperature. Angewandte Chemie International Edition, 41 (24). 4746-4748 doi:10.1002/anie.200290036
Shen, Qilong, Shekhar, Shashank, Stambuli, James P., Hartwig, John F. (2005) Highly Reactive, General, and Long-Lived Catalysts for Coupling Heteroaryl and Aryl Chlorides with Primary Nitrogen Nucleophiles. Angewandte Chemie, 117 (9). 1395-1399 doi:10.1002/ange.200462629
Shen, Qilong, Shekhar, Shashank, Stambuli, James P., Hartwig, John F. (2005) Highly Reactive, General, and Long-Lived Catalysts for Coupling Heteroaryl and Aryl Chlorides with Primary Nitrogen Nucleophiles. Angewandte Chemie International Edition, 44 (9). 1371-1375 doi:10.1002/anie.200462629
Xiao, Yu-Lan, Guo, Wen-Hao, He, Guo-Zhen, Pan, Qiang, Zhang, Xingang (2014) Nickel-Catalyzed Cross-Coupling of Functionalized Difluoromethyl Bromides and Chlorides with Aryl Boronic Acids: A General Method for Difluoroalkylated Arenes. Angewandte Chemie, 126 (37). 10067-10071 doi:10.1002/ange.201405653
Ge, Shaozhong, Hartwig, John F. (2012) Highly Reactive, Single-Component Nickel Catalyst Precursor for Suzuki-Miyuara Cross-Coupling of Heteroaryl Boronic Acids with Heteroaryl Halides. Angewandte Chemie, 124 (51). 13009-13013 doi:10.1002/ange.201207428
Levin, Mark D., Toste, F. Dean (2014) Gold-Catalyzed Allylation of Aryl Boronic Acids: Accessing Cross-Coupling Reactivity with Gold. Angewandte Chemie, 126 (24). 6325-6329 doi:10.1002/ange.201402924
Su, Weiping, Raders, Steven, Verkade, John G., Liao, Xuebin, Hartwig, John F. (2006) Pd-Catalyzed α-Arylation of Trimethylsilyl Enol Ethers with Aryl Bromides and Chlorides: A Synergistic Effect of Two Metal Fluorides as Additives. Angewandte Chemie, 118 (35). 5984-5987 doi:10.1002/ange.200601887
Stambuli, James P., Weng, Zhiqiang, Incarvito, Christopher D., Hartwig, John F. (2007) Reductive Elimination of Ether from T-Shaped, Monomeric Arylpalladium Alkoxides. Angewandte Chemie, 119 (40). 7818-7821 doi:10.1002/ange.200702809
Green, Rebecca A., Hartwig, John F. (2015) Nickel-Catalyzed Amination of Aryl Chlorides with Ammonia or Ammonium Salts. Angewandte Chemie, 127 (12). 3839-3843 doi:10.1002/ange.201500404
Xiao, Yu-Lan, Guo, Wen-Hao, He, Guo-Zhen, Pan, Qiang, Zhang, Xingang (2014) Nickel-Catalyzed Cross-Coupling of Functionalized Difluoromethyl Bromides and Chlorides with Aryl Boronic Acids: A General Method for Difluoroalkylated Arenes. Angewandte Chemie International Edition, 53 (37). 9909-9913 doi:10.1002/anie.201405653
Li, Qiaoli, Xu, Lanting, Ma, Dawei (2022) Cu‐Catalyzed Coupling Reactions of Sulfonamides with (Hetero)Aryl Chlorides/Bromides. Angewandte Chemie, 134 (43) doi:10.1002/ange.202210483
 
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