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Tobisu, Mamoru, Nakamura, Keisuke, Chatani, Naoto (2014) Nickel-Catalyzed Reductive and Borylative Cleavage of Aromatic Carbon–Nitrogen Bonds in N-Aryl Amides and Carbamates. Journal Of The American Chemical Society, 136 (15) 5587-5590 doi:10.1021/ja501649a

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Reference TypeJournal (article/letter/editorial)
TitleNickel-Catalyzed Reductive and Borylative Cleavage of Aromatic Carbon–Nitrogen Bonds in N-Aryl Amides and Carbamates
JournalJournal Of The American Chemical Society
AuthorsTobisu, MamoruAuthor
Nakamura, KeisukeAuthor
Chatani, NaotoAuthor
Year2014 (April 16)Volume136
Issue15
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja501649aSearch in ResearchGate
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Mindat Ref. ID1763669Long-form Identifiermindat:1:5:1763669:4
GUID0
Full ReferenceTobisu, Mamoru, Nakamura, Keisuke, Chatani, Naoto (2014) Nickel-Catalyzed Reductive and Borylative Cleavage of Aromatic Carbon–Nitrogen Bonds in N-Aryl Amides and Carbamates. Journal Of The American Chemical Society, 136 (15) 5587-5590 doi:10.1021/ja501649a
Plain TextTobisu, Mamoru, Nakamura, Keisuke, Chatani, Naoto (2014) Nickel-Catalyzed Reductive and Borylative Cleavage of Aromatic Carbon–Nitrogen Bonds in N-Aryl Amides and Carbamates. Journal Of The American Chemical Society, 136 (15) 5587-5590 doi:10.1021/ja501649a
In(2014, April) Journal Of The American Chemical Society Vol. 136 (15) American Chemical Society (ACS)

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Tobisu, Mamoru, Nakamura, Ryo, Kita, Yusuke, Chatani, Naoto (2009) Rhodium-Catalyzed Reductive Cleavage of Carbon−Cyano Bonds with Hydrosilane: A Catalytic Protocol for Removal of Cyano Groups. Journal Of The American Chemical Society, 131 (9) 3174-3175 doi:10.1021/ja810142v
Kinuta, Hirotaka, Tobisu, Mamoru, Chatani, Naoto (2015) Rhodium-Catalyzed Borylation of Aryl 2-Pyridyl Ethers through Cleavage of the Carbon–Oxygen Bond: Borylative Removal of the Directing Group. Journal Of The American Chemical Society, 137 (4) 1593-1600 doi:10.1021/ja511622e
Tobisu, Mamoru, Yamakawa, Ken, Shimasaki, Toshiaki, Chatani, Naoto (2011) Nickel-catalyzed reductive cleavage of aryl–oxygen bonds in alkoxy- and pivaloxyarenes using hydrosilanes as a mild reducing agent. Chemical Communications, 47 (10). 2946pp. doi:10.1039/c0cc05169a
Morioka, Toshifumi, Nishizawa, Akihiro, Nakamura, Keisuke, Tobisu, Mamoru, Chatani, Naoto (2015) Nickel-catalyzed Cross-coupling of Anisole Derivatives with Trimethylaluminum through the Cleavage of Carbon–Oxygen Bonds. Chemistry Letters, 44 (12). 1729-1731 doi:10.1246/cl.150936
Nishizawa, Akihiro, Takahira, Tsuyoshi, Yasui, Kosuke, Fujimoto, Hayato, Iwai, Tomohiro, Sawamura, Masaya, Chatani, Naoto, Tobisu, Mamoru (2019) Nickel-Catalyzed Decarboxylation of Aryl Carbamates for Converting Phenols into Aromatic Amines. Journal Of The American Chemical Society, 141 (18) 7261-7265 doi:10.1021/jacs.9b02751
Tobisu, Mamoru, Morioka, Toshifumi, Ohtsuki, Akimichi, Chatani, Naoto (2015) Nickel-catalyzed reductive cleavage of aryl alkyl ethers to arenes in absence of external reductant. Chemical Science, 6. 3410-3414 doi:10.1039/c5sc00305a
Shimasaki, Toshiaki, Tobisu, Mamoru, Chatani, Naoto (2010) Nickel-Catalyzed Amination of Aryl Pivalates by the Cleavage of Aryl CO Bonds. Angewandte Chemie, 122 (16). 2991-2994 doi:10.1002/ange.200907287
Tobisu, Mamoru, Kita, Yusuke, Chatani, Naoto (2006) Rh(I)-Catalyzed Silylation of Aryl and Alkenyl Cyanides Involving the Cleavage of C−C and Si−Si Bonds. Journal Of The American Chemical Society, 128 (25) 8152-8153 doi:10.1021/ja062745w
Nakamura, Keisuke, Tobisu, Mamoru, Chatani, Naoto (2015) Nickel-Catalyzed Formal Homocoupling of Methoxyarenes for the Synthesis of Symmetrical Biaryls via C–O Bond Cleavage. Organic Letters, 17. 6142-6145 doi:10.1021/acs.orglett.5b03151
Shimasaki, Toshiaki, Tobisu, Mamoru, Chatani, Naoto (2010) Nickel-Catalyzed Amination of Aryl Pivalates by the Cleavage of Aryl CO Bonds. Angewandte Chemie International Edition, 49 (16). 2929-2932 doi:10.1002/anie.200907287
Tobisu, Mamoru, Xu, Tian, Shimasaki, Toshiaki, Chatani, Naoto (2011) Nickel-Catalyzed Suzuki–Miyaura Reaction of Aryl Fluorides. Journal Of The American Chemical Society, 133 (48) 19505-19511 doi:10.1021/ja207759e
 
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