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Α-AMINOAZOLES IN THE SYNTHESIS OF HETEROCYCLES: V. SYNTHESIS OF AZOLO[1,5-A]PYRIMIDINES FROM 2-ETHOXYVINYL TRIFLUOROMETHYL KETONES AND 2,2-DIETHOXYVINYL TRIFLUOROMETHYL KETONE. / Emelina, E.E.; Petrov, A.A.

In: Russian Journal of Organic Chemistry, Vol. 45, No. 3, 2009, p. 417-420.

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@article{ca6ea80272f5444d8a875c53689f5bcc,
title = "Α-AMINOAZOLES IN THE SYNTHESIS OF HETEROCYCLES: V. SYNTHESIS OF AZOLO[1,5-A]PYRIMIDINES FROM 2-ETHOXYVINYL TRIFLUOROMETHYL KETONES AND 2,2-DIETHOXYVINYL TRIFLUOROMETHYL KETONE",
abstract = "A procedure was proposed for the synthesis of 7-trifluoromethylazolo[1,5-a] pyrimidines by reactions of 2-ethoxyvinyl trifluoromethyl ketones and 2,2-diethoxyvinyl trifluoromethyl ketone with 5(3)-aminoazoles. The reactions occurred under mild conditions, and the products were formed with high yield and regioselectivity. {\textcopyright} 2009 Pleiades Publishing, Ltd.",
author = "E.E. Emelina and A.A. Petrov",
year = "2009",
language = "English",
volume = "45",
pages = "417--420",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "3",

}

RIS

TY - JOUR

T1 - Α-AMINOAZOLES IN THE SYNTHESIS OF HETEROCYCLES: V. SYNTHESIS OF AZOLO[1,5-A]PYRIMIDINES FROM 2-ETHOXYVINYL TRIFLUOROMETHYL KETONES AND 2,2-DIETHOXYVINYL TRIFLUOROMETHYL KETONE

AU - Emelina, E.E.

AU - Petrov, A.A.

PY - 2009

Y1 - 2009

N2 - A procedure was proposed for the synthesis of 7-trifluoromethylazolo[1,5-a] pyrimidines by reactions of 2-ethoxyvinyl trifluoromethyl ketones and 2,2-diethoxyvinyl trifluoromethyl ketone with 5(3)-aminoazoles. The reactions occurred under mild conditions, and the products were formed with high yield and regioselectivity. © 2009 Pleiades Publishing, Ltd.

AB - A procedure was proposed for the synthesis of 7-trifluoromethylazolo[1,5-a] pyrimidines by reactions of 2-ethoxyvinyl trifluoromethyl ketones and 2,2-diethoxyvinyl trifluoromethyl ketone with 5(3)-aminoazoles. The reactions occurred under mild conditions, and the products were formed with high yield and regioselectivity. © 2009 Pleiades Publishing, Ltd.

M3 - Article

VL - 45

SP - 417

EP - 420

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 3

ER -

ID: 5013603