Copper-catalyzed enantioselective arylboronation of activated alkenes leading to chiral 3,3′-disubstituted oxindoles-Reference-Cited by-同舟云学术

Copper-catalyzed enantioselective arylboronation of activated alkenes leading to chiral 3,3′-disubstituted oxindoles

Published:2021 Issue:11 Volume:8 Page:2532-2536
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Chen Jiangfei¹²³⁴,Li Jin-Heng¹²³⁴⁵^ORCID,Zhu Yan-Ping⁵⁶⁷⁸⁹^ORCID,Wang Qiu-An¹²³⁴

Affiliation:

1. State Key Laboratory of Chemo/Biosensing and Chemometrics

2. Hunan University

3. Changsha 410082

4. China

5. School of Pharmacy

6. Key Laboratory of Molecular Pharmacology and Drug Evaluation

7. Ministry of Education

8. Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong

9. Yantai University

Abstract

Copper-catalyzed asymmetric arylboronation of activated alkenes for producing highly enantioenriched 3-boroalkyl oxindoles and incorporating pharmacophores is depicted.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO00186H

Reference50 articles.

1. Atroposelective Synthesis of Axially Chiral Biaryl Compounds

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3. Applied Hydroformylation

4. Synthesis of Light-Emitting Conjugated Polymers for Applications in Electroluminescent Devices

5. Atroposelective Total Synthesis of Axially Chiral Biaryl Natural Products

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