Atroposelective Access to Oxindole-Based Axially Chiral Styrenes via the Strategy of Catalytic Kinetic Resolution-Reference-Cited by-同舟云学术

Atroposelective Access to Oxindole-Based Axially Chiral Styrenes via the Strategy of Catalytic Kinetic Resolution

Published:2020-08-26 Issue:37 Volume:142 Page:15686-15696
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ma Chun¹,Sheng Feng-Tao¹,Wang Hai-Qing¹,Deng Shuang²,Zhang Yu-Chen¹,Jiao Yinchun²^ORCID,Tan Wei¹,Shi Feng¹^ORCID

Affiliation:

1. School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, China

2. Key Laboratory of Theoretical Organic Chemistry and Functional Molecule, Ministry of Education, School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China

Funder

Government of Jiangsu Province

National Natural Science Foundation 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.0c00208

Reference160 articles.

1. Privileged Chiral Ligands and Catalysts

2. New Approaches for Biaryl-Based Phosphine Ligand Synthesis via P═O Directed C–H Functionalizations

3. Natural Bridged Biaryls with Axial Chirality and Antimitotic Properties

4. Knipholone and related 4-phenylanthraquinones: structurally, pharmacologically, and biosynthetically remarkable natural products

5. Total synthesis of chiral biaryl natural products by asymmetric biaryl coupling

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