Synthesis of chiral N-acyl-2-pyrazolin-5-ols with a modified carane carbon frame

Журнал

Mendeleev Communications
ISSN: 0959-9436

Вых. Данные

Год: 1997, Номер: 4, Страницы: 139-141 Страниц : 3 DOI: 10.1070/MC1997v007n04ABEH000765

Авторы

Popov S.A. ¹ , Tkachev A.V. ¹

Организации

1	Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation

Treatment of bicyclic monoterpene diketone with a modified carane skeleton with acylhydrazines results in stable N-acylpyrazolinols in 26-86% yield.

Popov S.A. , Tkachev A.V.
Synthesis of chiral N-acyl-2-pyrazolin-5-ols with a modified carane carbon frame
Mendeleev Communications. 1997. N4. P.139-141. DOI: 10.1070/MC1997v007n04ABEH000765 WOS Scopus РИНЦ

Опубликована в печати:

1 янв. 1997 г.