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A3 coupling reaction (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "A3 coupling reaction" in English language version.

refsWebsite
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13doi.org
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1nih.gov
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1semanticscholar.org
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doi.org

  • W.-J. Yoo, L. Zhao, C.-J. Li, Aldrichimica Acta 2011, 44, 43–51. The A3-coupling (aldehyde-alkyne-amine) reaction: a versatile method for the preparation of propargylamines; C. Wei, C.-J. Li, J. Am. Chem. Soc. 2002, 124, 5638-5639. Enantioselective Direct Addition of Alkynes to Imines Catalyzed by Copper(I)pybox Complex in Water and in Toluene doi:10.1021/ja026007t; C. Wei, C.-J. Li, J. Am. Chem. Soc. 2003, 125, 9584-9585. A Highly Efficient Three-Component Coupling of Aldehyde, Alkyne, and Amines via C-H Activation Catalyzed by Gold in Waterdoi:10.1021/ja0359299
  • A walk around the A3-coupling Vsevolod A. Peshkov , Olga P. Pereshivkoa and Erik V. Van der Eycken Chem. Soc. Rev., 2012,41, 3790-3807 doi:10.1039/C2CS15356D
  • The Development of A3-Coupling (Aldehyde-Alkyne-Amine) and AA3-Coupling (Asymmetric Aldehyde-Alkyne-Amine) Chunmei Wei, Zigang Li, Chao-Jun Li Synlett 2004(9): 1472-1483 doi:10.1055/s-2004-829531
  • Rokade, Balaji V.; Barker, James; Guiry, Patrick J. (2019). "Development of and recent advances in asymmetric A3 coupling". Chemical Society Reviews. 48 (18): 4766–4790. doi:10.1039/C9CS00253G. PMID 31465045. S2CID 201665168.
  • Sakaguchi, S., Kubo, T. and Ishii, Y. (2001), A Three-Component Coupling Reaction of Aldehydes, Amines, and Alkynes. Angew. Chem. Int. Ed., 40: 2534–2536. doi:10.1002/1521-3773(20010702)40:13<2534::AID-ANIE2534>3.0.CO;2-2
  • Direct Addition of TMS-acetylene to Aldimines Catalyzed by a Simple, Commercially Available Ir(I) Complex Christian Fischer and Erick M. Carreira Organic Letters 2001 3 (26), 4319-4321 doi:10.1021/ol017022q
  • Highly efficient Grignard-type imine additions via C–H activation in water and under solvent-free conditions Chao-Jun Li and Chunmei Wei Chem. Commun., 2002, 268-269 doi:10.1039/B108851N
  • The redox-A3 reaction Daniel Seidel Org. Chem. Front., 2014, 1, 426 doi:10.1039/c4qo00022f
  • "Copper-Catalyzed Decarboxylative Coupling of sp3-Hybridized Carbons of α-Amino Acids" Hai-Peng Bi, Liang Zhao, Yong-Min Liang, and Chao-Jun Li Angew. Chem. Int. Ed. 2009, 48, 792-795 doi:10.1002/anie.200805122;Aldehyde- and Ketone-Induced Tandem Decarboxylation-Coupling (Csp3−Csp) of Natural α-Amino Acids and Alkynes Hai-Peng Bi, Qingfeng Teng, Min Guan, Wen-Wen Chen, Yong-Min Liang, Xiaojun Yao, and Chao-Jun Li The Journal of Organic Chemistry 2010 75 (3), 783-788 doi:10.1021/jo902319h
  • Nontraditional Reactions of Azomethine Ylides: Decarboxylative Three-Component Couplings of α-Amino Acids Chen Zhang and Daniel Seidel Journal of the American Chemical Society 2010 132 (6), 1798-1799 doi:10.1021/ja910719x
  • Das, D., Sun, A. X. and Seidel, D. (2013), Redox-Neutral Copper(II) Carboxylate Catalyzed α-Alkynylation of Amines. Angew. Chem. Int. Ed., 52: 3765–3769. doi:10.1002/anie.201300021
  • CuI-Catalyzed C1-Alkynylation of Tetrahydroisoquinolines (THIQs) by A3 Reaction with Tunable Iminium Ions Qin-Heng Zheng, Wei Meng, Guo-Jie Jiang, and Zhi-Xiang Yu Organic Letters 2013 15 (23), 5928-5931 doi:10.1021/ol402517e
  • Lin, W., Cao, T., Fan, W., Han, Y., Kuang, J., Luo, H., Miao, B., Tang, X., Yu, Q., Yuan, W., Zhang, J., Zhu, C. and Ma, S. (2014), Enantioselective Double Manipulation of Tetrahydroisoquinolines with Terminal Alkynes and Aldehydes under Copper(I) Catalysis. Angew. Chem. Int. Ed., 53: 277–281. doi:10.1002/anie.201308699

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