Аннотация:
The treatment of substituted ethyl 1-(3’,4’-dihydro-3’,3’-dimethylisoquinolyl)-1-oximinoacetates with hydrazine hydrate leads to a 3,4-dihydroisoquinoline ring enlargement with the annulation of a pyrazole ring to form substituted 5,5-dimethyl-2,3,5,6-tetrahydro- 3-oxopyrazolo[3,4-b]benzo-3-azepines.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
Yu. V. Shklyaev, V. A. Glushkov, V. V. Davidov, V. I. Sokol, V. S. Sergienko, “An unusual 3,4-dihydroisoquinoline ring enlargement with the annulation of pyrazole”, Mendeleev Commun., 10:1 (2000), 36–37
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4371
https://www.mathnet.ru/rus/mendc/v10/i1/p36
Эта публикация цитируется в следующих 5 статьяx:
Edgars Abele, Edmunds Lukevics, Patai's Chemistry of Functional Groups, 2010
V. A. Glushkov, V. I. Karmanov, Yu. V. Shklyaev, “Symmetrical and Unsymmetrical Bis-1,1′-(3,4-dihydroisoquinolines)”, Chem Heterocycl Compd, 41:4 (2005), 475
E. Abele, R. Abele, K. Rubina, E. Lukevics, “Quinoline Oximes: Synthesis, Reactions, and Biological Activity. (Review)”, Chem Heterocycl Compd, 41:2 (2005), 137
John B. Bremner, Progress in Heterocyclic Chemistry, 13, A critical review of the 2000 literature preceded by two chapters on current heterocyclic topics, 2001, 340
Yurii V. Shklyaev, Vladimir A. Glushkov, Viktor V. Davidov, Valentina I. Sokol, Vladimir S. Sergienko, “ChemInform Abstract: An Unusual 3,4‐Dihydroisoquinoline Ring Enlargement with the Annulation of Pyrazole.”, ChemInform, 31:24 (2000)
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