Hydrogen bond-promoted regio- and stereoselective synthesis of isoindoline derivatives through Pd-catalyzed isocyanide insertion reaction involving aziridines-Reference-Cited by-同舟云学术

Hydrogen bond-promoted regio- and stereoselective synthesis of isoindoline derivatives through Pd-catalyzed isocyanide insertion reaction involving aziridines

Published:2024 Issue:6 Volume:11 Page:1775-1781
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Zheng Shuang¹,Fan Hao-Jie¹,Liu Shan-Shan¹²,Xu Yang¹,Zhao Zhi-Wen¹,Kong Han-Han²,He Ping¹³,Wang Long²^ORCID,Ren Zhi-Lin¹²³^ORCID

Affiliation:

1. College of Chemical Engineering, Hubei University of Arts and Science, Xiangyang, 441053, Hubei, China

2. Key Laboratory of Inorganic Nonmetallic Crystalline and Energy Conversion Materials, College of Materials and Chemical Engineering, China Three Gorges University, Yichang, Hubei Province, 443002, P. R. China

3. Hubei Longzhong Laboratory, Xiangyang, 441000, Hubei, China

Abstract

We have successfully demonstrated an efficient and practical Pd-catalyzed reaction between aziridine and isocyanide, leading to the synthesis of isoindoline derivatives in moderate to good yields.

Funder

National College Students Innovation and Entrepreneurship Training Program

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO02079G

Reference62 articles.

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3. Synthesis of Unsaturated N-Heterocycles by Cycloadditions of Aziridines and Alkynes

4. Cycloaddition Reactions of Azides and Electron‐Deficient Alkenes in Deep Eutectic Solvents: Pyrazolines, Aziridines and Other Surprises

5. Eco-friendly co-catalyst-free cycloaddition of CO2 and aziridines activated by a porous MOF catalyst

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