Synthesis of New [1,2,5]Chalсogenadiazoles Fused With Pyridine Skeleton and Their Reactions With Neutral C‐Nucleophiles

Synthesis of New [1,2,5]Chalсogenadiazoles Fused With Pyridine Skeleton and Their Reactions With Neutral C‐Nucleophiles Full article

Journal

Journal of Heterocyclic Chemistry
ISSN: 0022-152X , E-ISSN: 1943-5193

Output data

Year: 2025, Volume: 62, Number: 10, Pages: 1080-1086 Pages count : 7 DOI: 10.1002/jhet.70053

Authors

Fedorenko Alexey K. ¹ , Ivanova Victoria V. ¹ , Starosotnikov Alexey M. ¹ , Minyaev Mikhail E. ¹ , Bastrakov Maxim A. ¹

Affiliations

1	N.D. Zelinsky Institute of Organic Chemistry RAS Moscow Russia

Reactions of [1,2,5]oxa- and [1,2,5]selenadiazolo[3,4-c]pyridines with neutral carbon nucleophiles such as indoles, pyrrole, polyphenols, and CH-acids have been studied. All reactions proceed under mild conditions. As a result, a number of complex molecules containing structurally diverse fragments were synthesized, and subsequent oxidative aromatization has been demonstrated.

Fedorenko A.K. , Ivanova V.V. , Starosotnikov A.M. , Minyaev M.E. , Bastrakov M.A.
Synthesis of New [1,2,5]Chalсogenadiazoles Fused With Pyridine Skeleton and Their Reactions With Neutral C‐Nucleophiles
Journal of Heterocyclic Chemistry. 2025. V.62. N10. P.1080-1086. DOI: 10.1002/jhet.70053 WOS Scopus OpenAlex

Web of science:	WOS:001546190200001
Scopus:	2-s2.0-105012625072
OpenAlex:	W4413040412

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