1,3-Dipolar Cycloaddition Reactions of 2-Arylmethylidentiazolo[3,2-<i>a</i>]pyrimidines with Azomethinylides: Studying the Supramolecular Organization of Products in the Crystalline Phase

1,3-Dipolar Cycloaddition Reactions of 2-Arylmethylidentiazolo[3,2-<i>a</i>]pyrimidines with Azomethinylides: Studying the Supramolecular Organization of Products in the Crystalline Phase

The [3+2]-cycloaddition of azomethinylides formed in situ to dipolarophiles is a promising approach for the synthesis of dispyroderivatives of oxindole and acenaphthenedione. In the course of our studies, it was shown that the cycloaddition of azomethinylides occurs specifically through the exocycli...

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Bibliographic Details
Main Authors: Anna Nefedova, Darya Tretyakova, Dilyara Mingazhetdinova, Artem Agarkov, Alexander Ovsyannikov, Igor Litvinov, Svetlana Solovieva, Igor Antipin
Format: Article
Language:English
Published: MDPI AG 2024-11-01
Series:Chemistry Proceedings
Subjects:
thiazolo[3,2-<i>a</i>]pyrimidines
2-arylmethylidene derivatives of thiazolo[3,2-<i>a</i>]pyrimidines
dispyrocompounds
[3+2]-cycloaddition
azomethinylides
supramolecular chemistry
Online Access:https://www.mdpi.com/2673-4583/16/1/24
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