Nucleophilic substitution in 1-methyl-3,4,5-trinitro-1H-pyrazole

Nucleophilic substitution in 1-methyl-3,4,5-trinitro-1H-pyrazole Full article

Journal

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Output data

Year: 2011, Volume: 21, Number: 3, Pages: 149-150 Pages count : 2 DOI: 10.1016/j.mencom.2011.04.012

Authors

Dalinger Igor L. ¹ , Vatsadze Irina A. ¹ , Shkineva Tatyana K. ¹ , Popova Galina P. ¹ , Shevelev Svyatoslav A. ¹

Affiliations

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

1-Methyl-3,4,5-trinitropyrazole in reaction with thiols, phenols, oximes, ammonia, amines and NH-azoles gives substitution products of the 5-positioned nitro group.

Dalinger I.L. , Vatsadze I.A. , Shkineva T.K. , Popova G.P. , Shevelev S.A.
Nucleophilic substitution in 1-methyl-3,4,5-trinitro-1H-pyrazole
Mendeleev Communications. 2011. V.21. N3. P.149-150. DOI: 10.1016/j.mencom.2011.04.012 WOS Scopus OpenAlex

≡ Web of science:	WOS:000292227900012
≡ Scopus:	2-s2.0-79957559977
≡ OpenAlex:	W2949618607