Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes-Reference-Cited by-同舟云学术

Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes

Published:2019 Issue:6 Volume:6 Page:863-867
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Hao Er-Jun¹²³⁴⁵,Fu Dan-Dan¹²³⁴⁵,Wang Dong-Chao¹²³⁴⁵^ORCID,Zhang Tao³⁶⁷⁸,Qu Gui-Rong¹²³⁴⁵,Li Gong-Xin¹²³⁴⁵,Lan Yu³⁶⁷⁸⁹^ORCID,Guo Hai-Ming¹²³⁴⁵^ORCID

Affiliation:

1. Henan Key Laboratory of Organic Functional Molecules and Drugs Innovation

2. Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals

3. School of Chemistry and Chemical Engineering

4. Henan Normal University

5. Xinxiang

6. Chongqing University

7. Chongqing 400030

8. China

9. College of Chemistry and Molecular Engineering

Abstract

Chemoselective asymmetric [3 + 2] cycloaddition reactions of purines with aminocyclopropanes for the dearomatization of purines have been successfully developed.

Funder

National Natural Science Foundation of China

Ministry of Education of the People's Republic of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/QO/C9QO00039A

Reference47 articles.

1. Arene–Alkene Cycloaddition

2. Donor−Acceptor-Substituted Cyclopropane Derivatives and Their Application in Organic Synthesis

3. Transition Metal Chemistry of Cyclopropenes and Cyclopropanes

4. Heterocycles from cyclopropanes: applications in natural product synthesis

5. Total Synthesis of Indoline Alkaloids: A Cyclopropanation Strategy

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