10 Palladium in Photocatalysis
Book
Editor: König, B.
Title: Photocatalysis in Organic Synthesis
Print ISBN: 9783132417021; Online ISBN: 9783132417069; Book DOI: 10.1055/b-006-161273
1st edition © 2019 Georg Thieme Verlag KG
Georg Thieme Verlag KG, Stuttgart
Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry
Science of Synthesis Reference Libraries
Parent publication
Title: Science of Synthesis
DOI: 10.1055/b-00000101
Series Editors: Fürstner (Editor-in-Chief), A.; Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.
Type: Multivolume Edition
Abstract
The concept of photoredox/transition-metal dual catalysis has been validated as a powerful platform for the construction of carbon–carbon and carbon–heteroatom bonds, and it illustrates the power of rational design in catalysis and the strategic use of mechanistic knowledge and manipulation for the development of novel synthetic methods. This chapter describes recent progress in the combination of visible-light photoredox catalysis with palladium catalysis, highlighting this as a valuable synthetic tool in accessing complex molecules in a rapid and modular fashion.
Key words
Keywords: - photocatalysis - palladium - visible light - photoredox - dual catalysis - C–H functionalization - C(sp2)–H arylation - C(sp2)–H acylation - intramolecular alkenation - intramolecular C–H amination - oxidative carbonylation - α-allylation of amines - decarboxylative allylation - acceptorless dehydrogenation-
15 Chiusoli G. P, Catellani M, Costa M, Motti E, Della Caʼ N, Maestri G. Coord. Chem. Rev 2010; 254: 456
-
23 Tredwell M. J, Gulias M, Gaunt Bremeyer N, Johansson C. C. C, Collins B. S. L, Gaunt M. J. Angew. Chem. Int. Ed 2011; 50: 1076
-
44 Boele M. D. K, van Strijdonck G. P. F, de Vries A. H. M, Kamer P. C. J, de Vries J. G, van Leeuwen P. W. N. M. J. Am. Chem. Soc 2002; 124: 1586
-
55 Jordan-Hore J. A, Johansson C. C. C, Gulias M, Beck E. M, Gaunt M. J. J. Am. Chem. Soc 2008; 130: 16184
-
64 Orito K, Horibata A, Nakamura T, Ushito H, Nagasaki H, Yuguchi M, Yamashita S, Tokuda M. J. Am. Chem. Soc 2004; 126: 14342
-
75 Xuan J, Zeng T.-T, Feng Z.-J, Deng Q.-H, Chen J.-R, Lu L.-Q, Xiao W.-J, Alper H. Angew. Chem. Int. Ed 2015; 54: 1625
-
87 Chowdhury A. D, Weding N, Julis J, Franke R, Jackstell R, Beller M. Angew. Chem. Int. Ed 2014; 53: 6477
-
92 Kato S, Saga Y, Kojima M, Fuse H, Matsunaga S, Fukatsu A, Kondo M, Masaoka S, Kanai M. J. Am. Chem. Soc 2017; 139: 2204
-
93 Ragauskas A. J, Beckham G. T, Biddy M. J, Chandra R, Chen F, Davis M. F, Davison B. H, Dixon R. A, Gilna P, Keller M, Langan P, Naskar A. K, Saddler J. N, Tschaplinski T. J, Tuskan G. A, Wyman C. E. Science (Washington, D. C.) 2014; 344: 709
-
95 Rinaldi R, Jastrzebski R, Clough M. T, Ralph J, Kennema M, Bruijnincx P. C. A, Weckhuysen B. M. Angew. Chem. Int. Ed 2016; 55: 8164
-
98 Parsell T. H, Owen B. C, Klein I, Jarrell T. M, Marcum C. L, Haupert L. J, Amundson L. M, Kenttämaa H. I, Ribeiro F, Miller J. T, Abu-Omar M. M. Chem. Sci 2013; 4: 806