Substrate‐Controlled Regioselectivity Switch in a Three‐Component 1,3‐Dipolar Cycloaddition Reaction to Access 3,3′‐Pyrrolidinyl‐Spirooxindoles Derivatives-Reference-Cited by-同舟云学术

Substrate‐Controlled Regioselectivity Switch in a Three‐Component 1,3‐Dipolar Cycloaddition Reaction to Access 3,3′‐Pyrrolidinyl‐Spirooxindoles Derivatives

Published:2022-05-20 Issue:12 Volume:364 Page:2047-2052
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv Synth Catal

Author:

Wang Kai‐Kai¹²^ORCID,Li Yan‐Li³,Chen Rong‐Xiang¹,Sun Ai‐Li²,Wang Zhan‐Yong¹^ORCID,Zhao Ying‐Chao¹,Wang Ming‐Yue¹,Sheng Shi¹

Affiliation:

1. School of Pharmacy Xinxiang University Xinxiang 453000 People's Republic of China

2. Key Laboratory of Nano-carbon Modified Film Technology Engineering of Henan Province Xinxiang 453000 People's Republic of China

3. Medical College Xinxiang University Xinxiang 453000 People's Republic of China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Henan Province

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202200269

Reference65 articles.

1. For reviews see:

2. Recent advances in organocatalytic asymmetric multicomponent cascade reactions for enantioselective synthesis of spirooxindoles

3. Isatins As Privileged Molecules in Design and Synthesis of Spiro-Fused Cyclic Frameworks

4. Catalytic asymmetric synthesis of spirooxindoles: recent developments

5. Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies

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