Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds

Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds Full article

Journal

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

Output data

Year: 2018, Volume: 28, Number: 6, Pages: 638-640 Pages count : 3 DOI: 10.1016/j.mencom.2018.11.025

Authors

Starosotnikov Alexey M. ¹ , Shkaev Dmitry V. ¹ , Bastrakov Maxim A. ¹ , Fedyanin Ivan V. ² , Shevelev Svyatoslav A. ¹ , Dalinger Igor L. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation
2	A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Highly electrophilic 6-nitro-4-azabenzofuroxan and 6-nitro-4-azabenzo[1,2,5]selenadiazole add π-excessive (het)arenes and other neutral nucleophiles at 7-position to give C–C and N–C-bonded adducts, 1,4-dihydropyridines fused with furoxan or selenadiazole ring.

Starosotnikov A.M. , Shkaev D.V. , Bastrakov M.A. , Fedyanin I.V. , Shevelev S.A. , Dalinger I.L.
Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds
Mendeleev Communications. 2018. V.28. N6. P.638-640. DOI: 10.1016/j.mencom.2018.11.025 WOS Scopus OpenAlex

Web of science:	WOS:000455070900025
Scopus:	2-s2.0-85057753380
OpenAlex:	W2903638004

DB	Citing
OpenAlex	21
Scopus	19
Web of science	17