Mild and Regioselective Benzylic C–H Functionalization: Ni-Catalyzed Reductive Arylation of Remote and Proximal Olefins-Reference-Cited by-同舟云学术

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Mild and Regioselective Benzylic C–H Functionalization: Ni-Catalyzed Reductive Arylation of Remote and Proximal Olefins

Published:2017-01-11 Issue:3 Volume:139 Page:1061-1064
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

He Yuli¹,Cai Yalei¹,Zhu Shaolin¹^ORCID

Affiliation:

1. State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China

Funder

Natural Science Foundation of Jiangsu Province

National Natural Science Foundation of China

Central Committee of the Communist Party of China

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.6b11962

Reference43 articles.

1. C–H functionalization logic in total synthesis

2. Recent developments in natural product synthesis using metal-catalysed C–H bond functionalisation

3. CH Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals

4. Total Synthesis of (+)-Lithospermic Acid by Asymmetric Intramolecular Alkylation via Catalytic C−H Bond Activation

5. Total Synthesis and Structural Revision of the Piperarborenines via Sequential Cyclobutane C–H Arylation

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