Vicarious nucleophilic amination of five-membered 4,6-dinitrobenzoheterocycles

Vicarious nucleophilic amination of five-membered 4,6-dinitrobenzoheterocycles Full article

Journal

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

Output data

Year: 2020, Volume: 69, Number: 2, Pages: 390-393 Pages count : 4 DOI: 10.1007/s11172-020-2773-z

Authors

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

Affiliations

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

Reactions of isomeric 4,6-dinitro-1- and 4,6-dinitro-2-phenylindazoles, as well as 4,6-dinitro-2-phenylbenzo[b]furan, with various aminating agents were studied under the vicarious nucleophilic substitution conditions. It was found that depending on the aminating system, the starting compounds undergo either selective mono-amination at position 7 or double amination.

Starosotnikov A.M. , Bastrakov M.A. , Kachala V.V. , Fedyanin I.V. , Shevelev S.A.
Vicarious nucleophilic amination of five-membered 4,6-dinitrobenzoheterocycles
Russian Chemical Bulletin. 2020. V.69. N2. P.390-393. DOI: 10.1007/s11172-020-2773-z WOS Scopus OpenAlex

Web of science:	WOS:000523019700027
Scopus:	2-s2.0-85083102984
OpenAlex:	W3014327870

DB	Citing
OpenAlex	2
Scopus	3
Web of science	3