Synthesis and oxidative cyclization of 7-amino-3-R-4,6-dinitrobenzo[d]isoxazoles

Synthesis and oxidative cyclization of 7-amino-3-R-4,6-dinitrobenzo[d]isoxazoles Full article

Journal

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

Output data

Year: 2009, Volume: 58, Number: 2, Pages: 426-429 Pages count : 4 DOI: 10.1007/s11172-010-0027-1

Authors

Bastrakov M.A. ¹ , Starosotnikov A.M. ¹ , Glukhov 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

A method was developed for the selective amination of 3-R-4,6-dinitrobenzo[d]isoxazoles at position 7 via the oxidative nucleophilic substitution of hydrogen. The resulting nitroamines were used to synthesize representatives of the previously unknown tricyclic heteroaromatic system, viz., isoxazolo[5,4-e]benzofuroxan.

Bastrakov M.A. , Starosotnikov A.M. , Glukhov I.V. , Shevelev S.A.
Synthesis and oxidative cyclization of 7-amino-3-R-4,6-dinitrobenzo[d]isoxazoles
Russian Chemical Bulletin. 2009. V.58. N2. P.426-429. DOI: 10.1007/s11172-010-0027-1 WOS Scopus OpenAlex

Web of science:	WOS:000275907000002
Scopus:	2-s2.0-77950212514
OpenAlex:	W2090931762

DB	Citing
OpenAlex	6
Scopus	4
Web of science	4