Molander, G. A.: 2020 Science of Synthesis, 2019/4: Dual Catalysis in Organic Synthesis 1 DOI: 10.1055/sos-SD-231-00100
Dual Catalysis in Organic Synthesis 1

1.2.2 Nickel/Photocatalyst Dual Catalysis

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Book

Editor: Molander, G. A.

Authors: Barriault, L.; Bhoyare, V. W.; Hashmi, A. S. K.; He, R.; Huo, X.; Kim, U B.; Lee, S.-g.; Molander, G. A.; Muralirajan, K.; Nakao, Y.; Patil, N. T.; Primer, D. N.; Riant, O.; Rohe, S.; Rout, S. K.; Rueping, M.; Shi, X.; Tathe, A. G.; Tellis, J. C.; Wang, J.; Zhang, W.; Zidan, M.

Title: Dual Catalysis in Organic Synthesis 1

Print ISBN: 9783132429765; Online ISBN: 9783132429802; Book DOI: 10.1055/b-006-164899

Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry

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Parent publication

Title: Science of Synthesis

DOI: 10.1055/b-00000101

Series Editors: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.

Type: Multivolume Edition

 


Abstract

This chapter outlines the broad scope of photoredox/nickel dual catalysis. Among the newer approaches to organic synthesis that engender the concept of dual catalysis, photoredox/nickel dual-catalytic cross-coupling reactions comprise one of the most rapidly developing and powerful tactics. Taken as a whole, these transformations enable novel carbon–carbon and carbon–heteroatom bond constructions that were previously challenging, if not impossible, to carry out. Most remarkably, these processes are most often carried out under near-neutral reaction conditions at ambient temperatures, with the energy to drive the reactions being provided solely by visible-light sources, thus enabling the incorporation of a broad range of diverse functional groups. As described, the development of these processes therefore provides one means to address the longstanding challenge of late-stage assembly of highly functionalized molecules via cross-coupling strategies.

 
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