Asymmetric dearomative cyclopropanation of naphthalenes to construct polycyclic compounds-Reference-Cited by-同舟云学术

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Asymmetric dearomative cyclopropanation of naphthalenes to construct polycyclic compounds

Published:2022 Issue:44 Volume:13 Page:13015-13019
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Guan Fujun¹,Zhou Rong¹,Ren Xiaoyu²,Guo Zhen²^ORCID,Wang Chengming¹^ORCID,Zhou Cong-Ying¹^ORCID

Affiliation:

1. College of Chemistry and Materials Science, Guangdong Provincial Key Laboratory of Functional Supramolecular Coordination Materials and Applications, Jinan University, Guangzhou 510632, People's Republic of China

2. College of Materials Science & Engineering, Key Laboratory of Interface Science and Engineering in Advanced Materials, Ministry of Education, Taiyuan University of Technology, Shanxi 030024, People's Republic of China

Abstract

An enantioselective dearomative cyclopropanation of naphthalenes has been developed, which constructed a range of tetracyclic compounds bearing multichiral centers in high enantioselectivity.

Funder

Natural Science Foundation of Shanxi Province

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/SC/D2SC04509E

Reference51 articles.

1. Catalytic Asymmetric Dearomatization Reactions

2. Strategies for the asymmetric functionalization of indoles: an update

3. Catalytic asymmetric dearomatization (CADA) reactions of phenol and aniline derivatives

4. Catalytic Asymmetric Dearomatization by Transition-Metal Catalysis: A Method for Transformations of Aromatic Compounds

5. Progresses in organocatalytic asymmetric dearomatization reactions of indole derivatives

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1. A Desymmetric Dearomatization Cyclopropanation of [2.2]Paracyclophane;CCS Chemistry;2024-08-05

2. Pd-Catalyzed Intramolecular Dearomative [4 + 2] Cycloaddition of Naphthalenes with Arylalkynes;Organic Letters;2023-11-07

3. Three-component redox-neutral 1,2-alkylarylation of vinylarenes involving C–H functionalization enabled by copper catalysis;Organic Chemistry Frontiers;2023

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