1.13 Nickel-Catalyzed Cross Coupling Involving Alkenes
Buch
Herausgeber: Yoshikai, N.
Titel: Base-Metal Catalysis 1
Print ISBN: 9783132453807; Online ISBN: 9783132453821; Buch-DOI: 10.1055/b000000441
1st edition © 2023 Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart
Fachgebiete: Organische Chemie;Chemische Reaktionen, Katalyse;Organometallchemie;Chemische Labormethoden, Stöchiometrie
Science of Synthesis Reference Libraries
Übergeordnete Publikation
Titel: Science of Synthesis
DOI: 10.1055/b-00000101
Reihenherausgeber: 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.
Typ: Mehrbändiges Werk
Abstract
Nickel-catalyzed functionalization of alkenes to give value-added products in a manner that is rapid, selective, and modular has resulted in tremendous advances in synthetic chemistry. Great progress has been achieved in nickel-catalyzed (migratory) hydrofunctionalization and difunctionalization of alkenes over the past few years. In the first half of this chapter, nickel-catalyzed (migratory) hydrofunctionalization of alkenes is described. The second half details nickel-catalyzed difunctionalization of alkenes. Both reductive and redox-neutral reactions are discussed.
Schlüsselwörter
alkenes - asymmetric catalysis - chain-walking - cross-coupling reactions - difunctionalization - hydrofunctionalization - isomerization - metal hydrides - nickel catalysis - regioselectivity - transition-metal catalysis- 18 Kumar GS, Peshkov A, Brzozowska A, Nikolaienko P, Zhu C, Rueping M. Angew. Chem. Int. Ed. 2020; 59: 6513
- 20 Cuesta-Galisteo S, Schörgenhumer J, Wei X, Merino E, Nevado C. Angew. Chem. Int. Ed. 2021; 60: 1605
- 52 Chen Y.-G, Shuai B, Xu X.-T, Li Y.-Q, Yang Q.-L, Qiu H, Zhang K, Fang P, Mei T.-S. J. Am. Chem. Soc. 2019; 141: 3395
- 54 Li Y, Luo Y, Peng L, Li Y, Zhao B, Wang W, Pang H, Deng Y, Bai R, Lan Y, Yin G. Nat. Commun. 2020; 11: 417
- 65 Sardini SR, Lambright AL, Trammel GL, Omer HM, Liu P, Brown MK. J. Am. Chem. Soc. 2019; 141: 9391
- 80 Shu W, García-Domínguez A, Quirós MT, Mondal R, Cárdenas DJ, Nevado C. J. Am. Chem. Soc. 2019; 141: 13812
- 81 Tu H.-Y, Wang F, Huo L, Li Y, Zhu S, Zhao X, Li H, Qing F.-L, Chu L. J. Am. Chem. Soc. 2020; 142: 9604