5-Diazo Dihydrouracils: Preparation and Some Transformations.


Journal

The Journal of organic chemistry
ISSN: 1520-6904
Titre abrégé: J Org Chem
Pays: United States
ID NLM: 2985193R

Informations de publication

Date de publication:
29 Sep 2024
Historique:
medline: 30 9 2024
pubmed: 30 9 2024
entrez: 30 9 2024
Statut: aheadofprint

Résumé

An approach to a new type of diazo reagents─diazo dihydrouracils─has been developed, and various transformations of the obtained diazo heterocycles have been studied, demonstrating their high synthetic potential for obtaining structurally diverse derivatives based on the privileged dihydrouracil scaffold. The X-H insertion reactions provide high yields of a variety of 5-substituted dihydrouracils. Cyclopropanation and 1,3-dipolar cycloaddition reactions involving a carbonyl ylide intermediate have been carried out to give spiro-annulated derivatives. The limitations of the modification methods with respect to the nature of substituents on the nitrogen atoms of the diazo heterocycle have been outlined.

Identifiants

pubmed: 39344186
doi: 10.1021/acs.joc.4c01973
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Grigory Kantin (G)

Saint Petersburg State University, Saint Petersburg 199034, Russian Federation.

Alexander Sapegin (A)

Saint Petersburg State University, Saint Petersburg 199034, Russian Federation.

Dmitry Dar'in (D)

Saint Petersburg State University, Saint Petersburg 199034, Russian Federation.
Saint Petersburg Research Institute of Phthisiopulmonology, Saint Petersburg 191036, Russian Federation.

Classifications MeSH