The specific reactivity of 3,4,5-trinitro-1H-pyrazole

The specific reactivity of 3,4,5-trinitro-1H-pyrazole Full article

Journal

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

Output data

Year: 2010, Volume: 20, Number: 5, Pages: 253-254 Pages count : 2 DOI: 10.1016/j.mencom.2010.09.003

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

Nitration of 3,5-dinitropyrazole with HNO3–H2SO4 mixture gives 3,4,5-trinitro-1H-pyrazole, which in reaction with ammonia, amines or thiols under mild conditions undergoes regioselective nucleophilic substitution of the 4-positioned nitro group.

Dalinger I.L. , Vatsadze I.A. , Shkineva T.K. , Popova G.P. , Shevelev S.A.
The specific reactivity of 3,4,5-trinitro-1H-pyrazole
Mendeleev Communications. 2010. V.20. N5. P.253-254. DOI: 10.1016/j.mencom.2010.09.003 WOS Scopus OpenAlex

≡ Web of science:	WOS:000283695500003
≡ Scopus:	2-s2.0-77958043041
≡ OpenAlex:	W2952768027