Acetonylation of 5(3)-(1 H -tetrazol-1-yl)-3(5)-nitro-1 H -pyrazole

Acetonylation of 5(3)-(1 H -tetrazol-1-yl)-3(5)-nitro-1 H -pyrazole Full article

Journal

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

Output data

Year: 2017, Volume: 27, Number: 5, Pages: 462-463 Pages count : 2 DOI: 10.1016/j.mencom.2017.09.010

Authors

Kormanov Alexandr V. ¹ , Shkineva Tatyana K. ¹ , Dalinger Igor L. ¹

Affiliations

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

N-Acetonylation of 5(3)-(1H-tetrazol-1-yl)-3(5)-nitro-1H-pyrazole with bromoacetone in the presence of NaHCO3 at 60 °C gave, along with expected isomeric N-acetonyl derivatives, a tricyclic product of the intramolecular electrophilic attack at the carbon atom of the tetrazole cycle.

Kormanov A.V. , Shkineva T.K. , Dalinger I.L.
Acetonylation of 5(3)-(1 H -tetrazol-1-yl)-3(5)-nitro-1 H -pyrazole
Mendeleev Communications. 2017. V.27. N5. P.462-463. DOI: 10.1016/j.mencom.2017.09.010 WOS Scopus OpenAlex

≡ Web of science:	WOS:000413618800010
≡ Scopus:	2-s2.0-85030091259
≡ OpenAlex:	W2759457419