Sciact
  • EN
  • RU

Functionalization of 4,6-dinitro-2-phenylindole at position 7 Full article

Journal Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Output data Year: 2008, Volume: 57, Number: 7, Pages: 1539-1542 Pages count : 4 DOI: 10.1007/s11172-008-0198-1
Authors Bastrakov M.A. 1 , Starosotnikov A.M. 1 , Shakhnes A.Kh. 1 , Shevelev S.A. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: Transformation of the amino group in 7-amino-1-methyl-4,6-dinitro-2-phenylindole afforded a number of new 7-R-4,6-dinitroindoles and a first representative of a novel tricyclic heteroaromatic system of [1,2,5]oxadiazolo[4,3-g]indole.
Cite: Bastrakov M.A. , Starosotnikov A.M. , Shakhnes A.K. , Shevelev S.A.
Functionalization of 4,6-dinitro-2-phenylindole at position 7
Russian Chemical Bulletin. 2008. V.57. N7. P.1539-1542. DOI: 10.1007/s11172-008-0198-1 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000266456700025
Scopus: 2-s2.0-67650503670
OpenAlex: W2033576277
Citing:
DB Citing
OpenAlex 7
Scopus 4
Web of science 4
Altmetrics: