The reactions of arylazasydnones with S- and O-nucleophiles

The reactions of arylazasydnones with S- and O-nucleophiles Full article

Journal

Chemistry of Heterocyclic Compounds
ISSN: 1573-8353 , E-ISSN: 0009-3122

Output data

Year: 2023, Volume: 59, Number: 4-5, Pages: 289-298 Pages count : 10 DOI: 10.1007/s10593-023-03195-x

Authors

Kormanov Alexandr V. ¹ , Shkineva Tatyana K. ¹ , Dalinger Igor L. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia

A series of 3-arylazasydnone derivatives containing a chlorine atom and nitro group at various phenyl ring locations were functionalized by a method developed on the basis of reactions with different S- and O-nucleophiles. In all cases, an SNAr reaction was shown to occur where the leaving group could be either a halogen or azasydnone moiety, depending on their mutual position.

Kormanov A.V. , Shkineva T.K. , Dalinger I.L.
The reactions of arylazasydnones with S- and O-nucleophiles
Chemistry of Heterocyclic Compounds. 2023. V.59. N4-5. P.289-298. DOI: 10.1007/s10593-023-03195-x WOS Scopus OpenAlex

≡ Web of science:	WOS:001019068600008
≡ Scopus:	2-s2.0-85162248412
≡ OpenAlex:	W4381490567