Synthesis and molecular structure of substituted 2-hydroxyperhydro-[1,3,2] dioxaborinino[5,4-c]pyridines, perhydro[1,3]dioxano[5,4-c]pyridine, and their precursor-4-hydroxy-3-(α-hydroxybenzyl)-1-methyl-4-phenylpiperidine

4,8a-Diphenyl-substituted 2-(2-propoxy)perhydro[1,3,2]dioxaborinino[5.4-c] pyridine was obtained by the condensation of 4-hydroxy-3-(α-hydroxybenzyl) -1-methyl-4-phenylpiperidine with triisopropyl borate, and its 2-hydroxysubstituted analog in the presence of water. 1-Methyl-4,8a-diphenyl- perhidro[1,3]dioxano[5,4-c]pyridine was synthesized by the reaction of the same piperidol with formaldehyde. A comparative study of the molecular structures of the three products was carried out by X-ray crystallography. © 2008 Springer Science+Business Media, Inc.

Авторы
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
11
Язык
Английский
Страницы
1404-1412
Статус
Опубликовано
Том
44
Год
2008
Организации
  • 1 People's Friendship University of Russia, Moscow 117198, Russian Federation
  • 2 Université d'Adobo-Adjamé 02, Abidjan 02, Cote d'Ivoire
  • 3 Chem-Bridge Corporation, Moscow 119048, Russian Federation
  • 4 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Moscow 119991, Russian Federation
Ключевые слова
4-hydroxy-3-(α-hydroxybenzyl)-1-methyl-4-phenylpiperidine; Molecular structures; Perhydro[1,3,2]dioxaborinino-[5,4-c]pyridines; Perhydro[1,3]dioxano[5,4-c] pyridine; Triisopropyl borate
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/3050/
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