2.15 Manganese-Catalyzed C—H Functionalization
Book
Editor: Yoshikai, N.
Title: Base-Metal Catalysis 2
Print ISBN: 9783132455030; Online ISBN: 9783132455054; Book DOI: 10.1055/b000000440
1st edition © 2023 Thieme. All rights reserved.
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, 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
Manganese-catalyzed directed C—H functionalization is an efficient and straightforward approach for the formation of a variety of C—C and C—heteroatom bonds. In this review, we summarize the most significant advances in manganese-catalyzed C(sp2)—H functionalizations, including C—H alkenylation, alkylation, allylation, cyclization, amination, cyanation, borylation, and hydroxymethylation. The chapter is classified based on the type of newly formed chemical bond (C—C, C—N, C—B, and C—D bonds) and the reacting partner.
Key words
base-metal catalysis - manganese catalysis - C—H functionalization - directing groups - C—C bond formation - C—heteroatom bond formation - C—Mn bonds-
27 Kaplaneris N, Kaltenhuser F, Sirvinskaite G, Fan S, De Oliveira T, Conradi LC, Ackermann L. Sci. Adv. 2021; 7: eabe6202
-
28 Kaplaneris N, Son J, Mendive-Tapia L, Kopp A, Barth ND, Maksso I, Vendrell M, Ackermann L. Nat. Commun. 2021; 12: 3389
-
29 Wang H, Pesciaioli F, Oliveira JCA, Warratz S, Ackermann L. Angew. Chem. Int. Ed. 2017; 56: 15063
-
36 Cai S.-H, Ye L, Wang D.-X, Wang Y.-Q, Lai L.-J, Zhu C, Feng C, Loh T.-P. Chem. Commun. (Cambridge) 2017; 53: 8731
-
43 Kaplaneris N, Rogge T, Yin R, Wang H, Sirvinskaite G, Ackermann L. Angew. Chem. Int. Ed. 2019; 58: 3476
-
54 Lu Q, Cembellín S, Greßies S, Singha S, Daniliuc CG, Glorius F. Angew. Chem. Int. Ed. 2018; 57: 1399
-
57 Lu Q, Greßies S, Cembellín S, Klauck FJR, Daniliuc CG, Glorius F. Angew. Chem. Int. Ed. 2017; 56: 12778
-
64 Liang Y.-F, Müller V, Liu W, Münch A, Stalke D, Ackermann L. Angew. Chem. Int. Ed. 2017; 56: 9415
-
68 Conde A, Sabenya G, Rodríguez M, Postils V, Luis JM, Díaz-Requejo MM, Costas M, Pérez PJ. Angew. Chem. Int. Ed. 2016; 55: 6530
-
81 Kumar S, Parshuram Satpute D, Nikhil Vaidya G, Nagpure M, Kumar Lokhande S, Meena D, Kumar D. Tetrahedron Lett. 2020; 61: 152017