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Shang, Rui, Ji, Dong-Sheng, Chu, Ling, Fu, Yao, Liu, Lei (2011) Synthesis of α-Aryl Nitriles through Palladium-Catalyzed Decarboxylative Coupling of Cyanoacetate Salts with Aryl Halides and Triflates. Angewandte Chemie International Edition, 50 (19). 4470-4474 doi:10.1002/anie.201006763

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Reference TypeJournal (article/letter/editorial)
TitleSynthesis of α-Aryl Nitriles through Palladium-Catalyzed Decarboxylative Coupling of Cyanoacetate Salts with Aryl Halides and Triflates
JournalAngewandte Chemie International Edition
AuthorsShang, RuiAuthor
Ji, Dong-ShengAuthor
Chu, LingAuthor
Fu, YaoAuthor
Liu, LeiAuthor
Year2011 (May 2)Volume50
Issue19
PublisherWiley
DOIdoi:10.1002/anie.201006763Search in ResearchGate
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Mindat Ref. ID8598435Long-form Identifiermindat:1:5:8598435:0
GUID0
Full ReferenceShang, Rui, Ji, Dong-Sheng, Chu, Ling, Fu, Yao, Liu, Lei (2011) Synthesis of α-Aryl Nitriles through Palladium-Catalyzed Decarboxylative Coupling of Cyanoacetate Salts with Aryl Halides and Triflates. Angewandte Chemie International Edition, 50 (19). 4470-4474 doi:10.1002/anie.201006763
Plain TextShang, Rui, Ji, Dong-Sheng, Chu, Ling, Fu, Yao, Liu, Lei (2011) Synthesis of α-Aryl Nitriles through Palladium-Catalyzed Decarboxylative Coupling of Cyanoacetate Salts with Aryl Halides and Triflates. Angewandte Chemie International Edition, 50 (19). 4470-4474 doi:10.1002/anie.201006763
In(2011, May) Angewandte Chemie International Edition Vol. 50 (19) Wiley

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Shang, Rui, Ji, Dong-Sheng, Chu, Ling, Fu, Yao, Liu, Lei (2011) Synthesis of α-Aryl Nitriles through Palladium-Catalyzed Decarboxylative Coupling of Cyanoacetate Salts with Aryl Halides and Triflates. Angewandte Chemie, 123 (19). 4562-4566 doi:10.1002/ange.201006763
Shang, Rui, Huang, Zheng, Chu, Ling, Fu, Yao, Liu, Lei (2011) Palladium-Catalyzed Decarboxylative Coupling of Potassium Nitrophenyl Acetates with Aryl Halides. Organic Letters, 13. 4240-4243 doi:10.1021/ol201750s
Shang, Rui, Fu, Yao, Wang, Yan, Xu, Qing, Yu, Hai-Zhu, Liu, Lei (2009) Copper-Catalyzed Decarboxylative Cross-Coupling of Potassium Polyfluorobenzoates with Aryl Iodides and Bromides. Angewandte Chemie International Edition, 48 (49). 9350-9354 doi:10.1002/anie.200904916
LIU, Lei, FU, Yao, JIANG, YuanYe (2012) Mechanism of palladium-catalyzed decarboxylative cross-coupling between cyanoacetate salts and aryl halides. SCIENTIA SINICA Chimica, 42 (10) 1493 doi:10.1360/zb2012-42-10-1493
Yeung, Pui Yee, Chung, Kin Ho, Kwong, Fuk Yee (2011) Palladium-Catalyzed Decarboxylative Arylation of Potassium Cyanoacetate: Synthesis of α-Diaryl Nitriles from Aryl Halides. Organic Letters, 13. 2912-2915 doi:10.1021/ol2009522
Shang, Rui, Fu, Yao, Wang, Yan, Xu, Qing, Yu, Hai-Zhu, Liu, Lei (2009) Copper-Catalyzed Decarboxylative Cross-Coupling of Potassium Polyfluorobenzoates with Aryl Iodides and Bromides. Angewandte Chemie, 121 (49). 9514-9518 doi:10.1002/ange.200904916
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
Liu, Dong, Ma, Hong‐Xing, Fang, Ping, Mei, Tian‐Sheng (2019) Nickel‐Catalyzed Thiolation of Aryl Halides and Heteroaryl Halides through Electrochemistry. Angewandte Chemie International Edition, 58 (15). 5033-5037 doi:10.1002/anie.201900956
Chou, Chih-Ming, Chatterjee, Indranil, Studer, Armido (2011) Stereospecific Palladium-Catalyzed Decarboxylative C(sp3)C(sp2) Coupling of 2,5-Cyclohexadiene-1-carboxylic Acid Derivatives with Aryl Iodides. Angewandte Chemie International Edition, 50 (37). 8614-8617 doi:10.1002/anie.201103450
Shang, Rui, Yang, Zhi-Wei, Wang, Yan, Zhang, Song-Lin, Liu, Lei (2010) Palladium-Catalyzed Decarboxylative Couplings of 2-(2-Azaaryl)acetates with Aryl Halides and Triflates. Journal Of The American Chemical Society, 132 (41) 14391-14393 doi:10.1021/ja107103b
Lindh, Jonas, Sjöberg, Per J. R., Larhed, Mats (2010) Synthesis of Aryl Ketones by Palladium(II)-Catalyzed Decarboxylative Addition of Benzoic Acids to Nitriles. Angewandte Chemie International Edition, 49 (42). 7733-7737 doi:10.1002/anie.201003009
 
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