Facile one-pot synthesis of spirooxindole-pyrrolidine derivatives and their antimicrobial and acetylcholinesterase inhibitory activities-Reference-Cited by-同舟云学术

Facile one-pot synthesis of spirooxindole-pyrrolidine derivatives and their antimicrobial and acetylcholinesterase inhibitory activities

Published:2018 Issue:19 Volume:42 Page:16211-16216
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Huang Ying¹²³⁴,Min Wei⁵⁶⁷⁴,Wu Qiu-Wen⁸²⁹⁴,Sun Jing¹²³⁴,Shi Da-Hua⁵⁶⁷⁴,Yan Chao-Guo¹²³⁴^ORCID

Affiliation:

1. College of Chemistry & Chemical Engineering

2. Yangzhou University

3. Yangzhou 225002

4. China

5. Pharmacy School

6. Huaihai Institute of Technology

7. Lianyungang 222005

8. College of Medicine

9. Yangzhou 225001

Abstract

A library of novel spirooxindole-pyrrolidine derivatives were facilely synthesized via 1,3-dipolar cycloaddition of azomethine ylide generated from sarcosine and paraformaldehyde with various 3-methyleneoxindolines.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/NJ/C8NJ03813A

Reference83 articles.

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5. Asymmetric synthesis of chiral oxindoles using isatin as starting material

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