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...

Full description

Saved in:
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
Tags: Add Tag
No Tags, Be the first to tag this record!
Login for hold and recall information

Internet

https://www.mdpi.com/2673-4583/16/1/24

Similar Items