Expeditious synthesis of bicyclic pyrrolidine/pyrrolizidine/thiazolidine grafted macrocycles through intramolecular 1,3-dipolar cycloaddition of azomethine ylides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference30 articles.
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1. Crystal structure and hirshfeld surface analysis of 1, 2, 3, triazole bridged pyrrolizidine grafted macrocycle;Chemical Data Collections;2020-08
2. Regio- and stereoselective synthesis of spiropyrrolidine-oxindole and bis-spiropyrrolizidine-oxindole grafted macrocycles through [3 + 2] cycloaddition of azomethine ylides;RSC Advances;2020
3. Intramolecular Cycloaddition of Azomethine Ylides Activated by Aromatic Rings: Scope and Limitations;Chemistry of Heterocyclic Compounds;2016-07
4. A theoretical study of the mechanism and selectivity of the intramolecular 1,3-dipolar cycloaddition reaction of the nitrone–alkene derived from 2-allylthiobenzaldehyde for the synthesis of tricyclic isoxazolidines;Tetrahedron Letters;2016-01
5. ChemInform Abstract: Expeditious Synthesis of Bicyclic Pyrrolidine/Pyrrolizidine/Thiazolidine Grafted Macrocycles Through Intramolecular 1,3-Dipolar Cycloaddition of Azomethine Ylides.;ChemInform;2014-03-21
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