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Unexpected results in the heterocyclization of 5-acetylenyl-pyrazole-4-carboxylic acid hydrazides under the influence of CuCl: formation of a diazepinone and dehydrodimerization into the corresponding bis(pyrazolo[4,3-d][1,2]diazepinone) Научная публикация

Журнал Tetrahedron Letters
ISSN: 0040-4039
Вых. Данные Год: 2005, Том: 46, Номер: 26, Страницы: 4457-4459 Страниц : 3 DOI: 10.1016/j.tetlet.2005.04.127
Ключевые слова pyrazolopyridines; cross-coupling; hetarylacetylenes; heterocyclization
Авторы Vasilevsky Sergei F. 1 , Mshvidobadze Elena V. 1 , Mamatyuk Victor I. 2 , Romanenko Galina V. 3 , Elguero Jose 4
Организации
1 (Данные Web of science) Russian Acad Sci, Inst Chem Kinet & Combust, Siberian Branch, Novosibirsk 630090, Russia
2 (Данные Web of science) Russian Acad Sci, Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia
3 (Данные Web of science) Russian Acad Sci, Int Tomog Ctr, Siberian Branch, Novosibirsk 630090, Russia
4 (Данные Web of science) CSIC, Inst Quim Med, E-28006 Madrid, Spain

Реферат: The simple reaction of cyclization of hydrazides of vic-acetylenylbenzoic and acetylenylpyrazole carboxylic acid can lead to four different compounds: five-membered N-aminolactams, six-membered N-aminolactams, six-membered diazinones and diazepinones, but only the first three have been described. In this paper we report the unexpected formation of a bis(pyrazolo[4,3-d][1,2]diazepinone, the structure of which has been established by X-ray crystallography. (c) 2005 Elsevier Ltd. All rights reserved.
Библиографическая ссылка: Vasilevsky S.F. , Mshvidobadze E.V. , Mamatyuk V.I. , Romanenko G.V. , Elguero J.
Unexpected results in the heterocyclization of 5-acetylenyl-pyrazole-4-carboxylic acid hydrazides under the influence of CuCl: formation of a diazepinone and dehydrodimerization into the corresponding bis(pyrazolo[4,3-d][1,2]diazepinone)
Tetrahedron Letters. 2005. V.46. N26. P.4457-4459. DOI: 10.1016/j.tetlet.2005.04.127 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 июн. 2005 г.
Идентификаторы БД:
Web of science: WOS:000229844600008
Scopus: 2-s2.0-19544362859
РИНЦ: 13495054
OpenAlex: W2047624456
Цитирование в БД:
БД Цитирований
Web of science 16
Scopus 19
РИНЦ 19
OpenAlex 18
Альметрики: