Synthesis of 3-R-2-aryl-4,6-dinitroindoles and specific features of their reactions with anionic nucleophiles

Synthesis of 3-R-2-aryl-4,6-dinitroindoles and specific features of their reactions with anionic nucleophiles Full article

Journal

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

Output data

Year: 2007, Volume: 56, Number: 8, Pages: 1603-1607 Pages count : 5 DOI: 10.1007/s11172-007-0250-6

Authors

Bastrakov M.A. ¹ , Starosotnikov A.M. ¹ , Kachala V.V. ¹ , Nesterova E.N. ¹ , Shevelev S.A. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

Reaction of different anionic S-nucleophiles with 3-R-2-aryl-4,6-dinitroindoles led to a regiospecific nucleophilic substitution of the nitro group in position 4 with 6-NO2 group remaining intact. The representatives of some peri-annulated polycyclic systems were synthesized on the basis of the substitution products.

Bastrakov M.A. , Starosotnikov A.M. , Kachala V.V. , Nesterova E.N. , Shevelev S.A.
Synthesis of 3-R-2-aryl-4,6-dinitroindoles and specific features of their reactions with anionic nucleophiles
Russian Chemical Bulletin. 2007. V.56. N8. P.1603-1607. DOI: 10.1007/s11172-007-0250-6 WOS Scopus OpenAlex

Web of science:	WOS:000252171400022
Scopus:	2-s2.0-37749003077
OpenAlex:	W2952555657

DB	Citing
OpenAlex	8
Scopus	6
Web of science	7