Nickel-Catalyzed Atroposelective C–H Alkylation Enabled by Bimetallic Catalysis with Air-Stable Heteroatom-Substituted Secondary Phosphine Oxide Preligands-Reference-Cited by-同舟云学术

Nickel-Catalyzed Atroposelective C–H Alkylation Enabled by Bimetallic Catalysis with Air-Stable Heteroatom-Substituted Secondary Phosphine Oxide Preligands

Published:2024-03-21 Issue:13 Volume:146 Page:9172-9180
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Zhang Zi-Jing¹,Simon Matthias M.¹,Yu Shuang²,Li Shu-Wen²,Chen Xinran¹,Cattani Silvia¹,Hong Xin²,Ackermann Lutz¹³^ORCID

Affiliation:

1. Institut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077 Göttingen, Germany

2. Center of Chemistry for Frontier Technologies, Department of Chemistry, Zhejiang University, Hangzhou 310027, China

3. Wöhler Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität Göttingen, Tammannstraße 2, 37077 Göttingen, Germany

Funder

European Research Council

Beijing National Laboratory for Molecular Sciences

National Key Research and Development Program of China

State Key Laboratory of Physical Chemistry of Solid Surfaces, Xiamen University

Deutsche Forschungsgemeinschaft

Science and Technology Department of Zhejiang Province

Fundamental Research Funds for the Central Universities

Alexander von Humboldt-Stiftung

National Natural Science Foundation of China

Chinese Academy of Sciences

Natural Science Foundation of Zhejiang Province

Shanghai Institute for Advanced Study, Zhejiang University

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.3c14600

Reference61 articles.

1. C‐H Activation for Asymmetric Synthesis

2. Catalytic Enantioselective Transformations Involving C–H Bond Cleavage by Transition-Metal Complexes

3. Catalytic Enantioselective Functionalizations of C–H Bonds by Chiral Iridium Complexes

4. Diverse Approaches for Enantioselective C−H Functionalization Reactions Using Group 9 Cp x M III Catalysts

5. Enantioselective C−H Activation with Earth‐Abundant 3d Transition Metals

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