Convenient generation of 1,3-dipolar nitrilimines and [3 + 2] cycloaddition for the synthesis of spiro compounds-Reference-Cited by-同舟云学术

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Convenient generation of 1,3-dipolar nitrilimines and [3 + 2] cycloaddition for the synthesis of spiro compounds

Published:2022-11 Issue: Volume:110 Page:154186
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Zhu Mei-Jun,Ye Rong,Shi Wen-Jing,Sun Jing,Yan Chao-Guo

Funder

National Natural Science Foundation of China

Priority Academic Program Development of Jiangsu Higher Education Institutions

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference66 articles.

1. Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides

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

3. Enantioselective Copper-Catalyzed 1,3-Dipolar Cycloadditions

4. Asymmetric organocatalytic cycloadditions

5. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

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1. Strategies and Methods for the Synthesis of 2‐Pyrazolines: Recent Developments (2012–2022);Advanced Synthesis & Catalysis;2023-06-02

2. A one-pot, multicomponent tandem synthesis of fused polycyclic pyrrolo[3,2-c]quinolinone/pyrrolizino[2,3-c]quinolinone hybrid heterocycles via environmentally benign solid state melt reaction;Green Processing and Synthesis;2023-01-01

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