Synthesis of spiropyrrolidine oxindolesviaAg-catalyzed stereo- and regioselective 1,3-dipolar cycloaddition of indole-based azomethine ylides with chalcones-Reference-Cited by-全球学者库

Synthesis of spiropyrrolidine oxindolesviaAg-catalyzed stereo- and regioselective 1,3-dipolar cycloaddition of indole-based azomethine ylides with chalcones

Published:2018 Issue:24 Volume:42 Page:20024-20031
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Yue Guizhou¹²³⁴^ORCID,Wu Yao¹²³⁴,Dou Zhengjie¹²³⁴,Chen Huabao⁵²⁶⁴^ORCID,Yin Zhongqiong⁷²⁶⁴,Song Xu⁷²⁶⁴,He ChangLiang⁷²⁶⁴,Wang Xianxiang¹²³⁴,Feng Juhua¹²³⁴,Zhang Zuming¹²³⁴,Zou Ping¹²³⁴,Lu Cuifen⁸⁹¹⁰⁴

Affiliation:

1. College of Science

2. Sichuan Agricultural University

3. Ya’an

4. China

5. College of Agricultural Sciences

6. Chengdu

7. College of Veterinary Medicine

8. Hubei Collaborative Innovation Center for Advanced Organochemical Materials & Ministry-of-Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules

9. Hubei University

10. Wuhan 430062

Abstract

In excess of 100 new compounds were prepared in moderate to high yields (50–95%) with good to excellent diastereoselectivity (11 : 1 → 20 : 1 dr) by Ag-catalyzed 1,3-dipolar cycloaddition.

Funder

Sichuan Agricultural University

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/NJ/C8NJ04492A

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1. The chemistry of isatins: a review from 1975 to 1999