Reactions of highly electrophilic 6,8-dinitro[1,2,4]triazolo[1,5-a]pyridines with C-nucleophiles

Reactions of highly electrophilic 6,8-dinitro[1,2,4]triazolo[1,5-a]pyridines with C-nucleophiles Full article

Journal

Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285

Output data

Year: 2023, Volume: 72, Number: 4, Pages: 960-965 Pages count : 6 DOI: 10.1007/s11172-023-3860-6

Authors

Bastrakov M.A. ¹ , Nadykta V.G. ¹ , Fedorenko A.K. ¹ , Starosotnikov A.M. ¹

Affiliations

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

Reactions of 2-R-6,8-dinitro[1,2,4]triazolo[1,5-a]pyridines with indoles and 1,3-dicarbonyl compounds were studied. It was found that stable products of nucleophilic addition to the pyridine ring were formed under mild conditions in the absence of a base. The new derivatives of 1,5-dihydro[1,2,4]triazolo[1,5-a]pyridine were synthesized in up to 96% yield.

Bastrakov M.A. , Nadykta V.G. , Fedorenko A.K. , Starosotnikov A.M.
Reactions of highly electrophilic 6,8-dinitro[1,2,4]triazolo[1,5-a]pyridines with C-nucleophiles
Russian Chemical Bulletin. 2023. V.72. N4. P.960-965. DOI: 10.1007/s11172-023-3860-6 WOS Scopus OpenAlex

Web of science:	WOS:000986557800015
Scopus:	2-s2.0-85159200974
OpenAlex:	W4376137619

DB	Citing
OpenAlex	7
Scopus	7
Web of science	7