1,3-Dipolar Cycloaddition of Benzofuranone Derivatives and Azomethine Ylides Promoted by Simple Functional Ionic Liquids: Direct Access to Highly Substituted Pyrrolidine and Spirocyclic Benzofuranone-Reference-Cited by-同舟云学术

1,3-Dipolar Cycloaddition of Benzofuranone Derivatives and Azomethine Ylides Promoted by Simple Functional Ionic Liquids: Direct Access to Highly Substituted Pyrrolidine and Spirocyclic Benzofuranone

Published:2016-09-16 Issue:15 Volume:1 Page:4403-4407
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Zhang Chuan-Bao¹,Dou Pei-Hao¹,Zhang Jun¹,Wei Qiang-Qiang¹,Wang Yan-Bo¹²,Zhu Jun-Yan¹²,Fu Ji-Ya¹²,Ding Tao¹²

Affiliation:

1. College of Chemistry and Chemical Engineering; Henan University, Kaifeng; Henan 475004 China

2. Henan Engineering Laboratory of Flame-Retardant and Functional Materials, College of Chemistry and Chemical Engineering; Henan University, Kaifeng; Henan 475004 China

Publisher

Wiley

Subject

General Chemistry

Reference66 articles.

1. Catalytic Asymmetric 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides—A Simple Approach to Optically Active Highly Functionalized Proline Derivatives

2. Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Azomethine Ylides for Biology-Oriented Synthesis

3. Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides

4. Construction of Enantiopure Pyrrolidine Ring System via Asymmetric [3+2]-Cycloaddition of Azomethine Ylides

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