8-R-5,7-Dinitroquinolines in [3+2] cycloaddition reactions with N-methylazomethine ylide

8-R-5,7-Dinitroquinolines in [3+2] cycloaddition reactions with N-methylazomethine ylide Full article

Journal

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

Output data

Year: 2013, Volume: 62, Number: 4, Pages: 1052-1059 Pages count : 8 DOI: 10.1007/s11172-013-0141-y

Authors

Bastrakov M.A. ¹ , Leonov A.I. ¹ , Starosotnikov A.M. ¹ , Fedyanin I.V. ² , Shevelev S.A. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation
2	A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991 Moscow, Russian Federation.

Novel derivatives of isoindole and dihydroisoindole fused to the pyridine ring were obtained by 1,3-dipolar cycloaddition reactions of N-methylazomethine ylide with substituted 5,7-dinitroquinolines. The substituents in the benzene ring were found to affect the cycloaddition outcome.

Bastrakov M.A. , Leonov A.I. , Starosotnikov A.M. , Fedyanin I.V. , Shevelev S.A.
8-R-5,7-Dinitroquinolines in [3+2] cycloaddition reactions with N-methylazomethine ylide
Russian Chemical Bulletin. 2013. V.62. N4. P.1052-1059. DOI: 10.1007/s11172-013-0141-y WOS Scopus OpenAlex

Web of science:	WOS:000331392200024
Scopus:	2-s2.0-84897692682
OpenAlex:	W2086470366

DB	Citing
OpenAlex	13
Scopus	15
Web of science	15