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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Autori principali:	Anna Nefedova, Darya Tretyakova, Dilyara Mingazhetdinova, Artem Agarkov, Alexander Ovsyannikov, Igor Litvinov, Svetlana Solovieva, Igor Antipin
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	MDPI AG 2024-11-01
Serie:	Chemistry Proceedings
Soggetti:	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
Accesso online:	https://www.mdpi.com/2673-4583/16/1/24
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