C-H functionalization of highly electrophilic azolopyridines as a way to donor-acceptor conjugated indoles

C-H functionalization of highly electrophilic azolopyridines as a way to donor-acceptor conjugated indoles Full article

Journal

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Output data

Year: 2025, Volume: 35, Number: 6, Pages: 648-650 Pages count : 3 DOI: 10.71267/mencom.7793

Authors

Ivanova Victoria V ¹ , Starosotnikov Alexey Mikhailovich ¹ , Minyaev Mikhail Evgenievich ¹ , Kruchinin Andrey A ¹ , Fakhrutdinov Artem Nikolaevich ¹ , Bastrakov Maxim Aleksandrovich ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

The DDQ-assisted oxidative aromatization of 1,4-adducts of indoles to [1,2,5]chalcogenadiazolo[4,3-b]pyridines or 6,8-dinitro[1,2,4]triazolo[1,5-a]pyridines affords the corresponding new indole-type donor–acceptor compounds. Studying their photophysical properties revealed correlations between the substitution pattern and absorption spectra.

Ivanova V.V. , Starosotnikov A.M. , Minyaev M.E. , Kruchinin A.A. , Fakhrutdinov A.N. , Bastrakov M.A.
C-H functionalization of highly electrophilic azolopyridines as a way to donor-acceptor conjugated indoles
Mendeleev Communications. 2025. V.35. N6. P.648-650. DOI: 10.71267/mencom.7793 WOS Scopus OpenAlex

Web of science:	WOS:001629970900008
Scopus:	2-s2.0-105021210802
OpenAlex:	W4415383310

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