Standard

Study of regioselectivity of reaction 3(5)-aminopyrazoles with 2-acylcycloakanones. / Petrov, A.A.; Kasatochkin, A.N.; Emelina, E.E.

в: Russian Journal of Organic Chemistry, Том 48, № 8, 2012, стр. 1111-1120.

Результаты исследований: Научные публикации в периодических изданиях › статья

Harvard

Petrov, AA, Kasatochkin, AN & Emelina, EE 2012, 'Study of regioselectivity of reaction 3(5)-aminopyrazoles with 2-acylcycloakanones', Russian Journal of Organic Chemistry, Том. 48, № 8, стр. 1111-1120.

APA

Petrov, A. A., Kasatochkin, A. N., & Emelina, E. E. (2012). Study of regioselectivity of reaction 3(5)-aminopyrazoles with 2-acylcycloakanones. Russian Journal of Organic Chemistry, 48(8), 1111-1120.

Vancouver

Petrov AA, Kasatochkin AN, Emelina EE. Study of regioselectivity of reaction 3(5)-aminopyrazoles with 2-acylcycloakanones. Russian Journal of Organic Chemistry. 2012;48(8):1111-1120.

Author

Petrov, A.A. ; Kasatochkin, A.N. ; Emelina, E.E. / Study of regioselectivity of reaction 3(5)-aminopyrazoles with 2-acylcycloakanones. в: Russian Journal of Organic Chemistry. 2012 ; Том 48, № 8. стр. 1111-1120.

BibTeX

@article{187cc0dc824d4f40b7d9bdef17a1bf44,
title = "Study of regioselectivity of reaction 3(5)-aminopyrazoles with 2-acylcycloakanones",
abstract = "Regioselectivity was examined of reactions between nine 3(5)-aminopyrazoles and 2-acetylcyclopentanone and 2-acetylcyclohexanone under various conditions. A series of cyclopenta[e]pyrazolo-[1,5-a]pyrimidines was obtained. The highest regioselectivity of the reaction was observed in alcohol at 20°С in the presence of a catalytic quantity of trifl uoroacetic acid. The regiostructure of compounds was established by 1Н and 13С NMR spectroscopy.",
keywords = "pyrazolo[1, 5-a]pyrimidine, 5-aminopyrazole C",
author = "A.A. Petrov and A.N. Kasatochkin and E.E. Emelina",
year = "2012",
language = "English",
volume = "48",
pages = "1111--1120",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "8",

}

RIS

TY - JOUR

T1 - Study of regioselectivity of reaction 3(5)-aminopyrazoles with 2-acylcycloakanones

AU - Petrov, A.A.

AU - Kasatochkin, A.N.

AU - Emelina, E.E.

PY - 2012

Y1 - 2012

N2 - Regioselectivity was examined of reactions between nine 3(5)-aminopyrazoles and 2-acetylcyclopentanone and 2-acetylcyclohexanone under various conditions. A series of cyclopenta[e]pyrazolo-[1,5-a]pyrimidines was obtained. The highest regioselectivity of the reaction was observed in alcohol at 20°С in the presence of a catalytic quantity of trifl uoroacetic acid. The regiostructure of compounds was established by 1Н and 13С NMR spectroscopy.

AB - Regioselectivity was examined of reactions between nine 3(5)-aminopyrazoles and 2-acetylcyclopentanone and 2-acetylcyclohexanone under various conditions. A series of cyclopenta[e]pyrazolo-[1,5-a]pyrimidines was obtained. The highest regioselectivity of the reaction was observed in alcohol at 20°С in the presence of a catalytic quantity of trifl uoroacetic acid. The regiostructure of compounds was established by 1Н and 13С NMR spectroscopy.

KW - pyrazolo[1

KW - 5-a]pyrimidine

KW - 5-aminopyrazole C

M3 - Article

VL - 48

SP - 1111

EP - 1120

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 8

ER -

ID: 5327161