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Yoshikai, N. : 2023 Science of Synthesis, 2022/5: Base-Metal Catalysis 1 DOI: 10.1055/sos-SD-238-00208
Base-Metal Catalysis 1

1.11 Nickel-Catalyzed Enantioselective Reductive Cross-Coupling Reactions

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Editor: Yoshikai, N. 

Authors: Chatani, N. ; Chemler, S. R. ; Chen, P. ; Dai, H.-X. ; Delcaillau, T.; Fujihara, T. ; Huang, J. ; Iwabuchi, Y. ; Kennedy-Ellis, J. J. ; Ko, C.; Koh, M. J. ; Lee, B. C.; Li, Y.; Lin, L.; Liu, G. ; Ma, D. ; Morandi, B. ; Nakao, Y. ; Ouyang, Y. ; Pang, X.; Qing, F.-L. ; Ren, Y. ; Sasano, Y. ; Shang, Y. ; Shou, J.-Y.; Shu, X.-Z. ; Su, W. ; Tobisu, M. ; Wang, C. ; Xiong, T. ; Xu, H.; Yang, F.; Yoshida, T.; Zhu, S. 

Title: Base-Metal Catalysis 1

Print ISBN: 9783132453807; Online ISBN: 9783132453821; Book DOI: 10.1055/b000000441

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

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Abstract

Nickel-catalyzed enantioselective reductive cross-coupling reactions enable simple and efficient synthesis of enantioenriched compounds, with high functionality tolerance, through circumventing the use of pregenerated organometallics. In this chapter, the most quintessential examples of the recent advances in this field have been summarized, and the contents are organized according to the reaction types.

Key words

nickel catalysis - reductive cross coupling - cross-electrophile coupling - asymmetric catalysis - ring-opening reactions - dicarbofunctionalization - Heck reaction - arylation - alkylation - carbamoylation - acylation - vinylation - organohalides - epoxides - aziridines - cyclobutanones - alkenes - oxindoles - indanes - indanones
 
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