1H and 13C NMR Study of Tautomerism of 9-Hydroxy-3-methylphenalen-1-ones

Tautomeric equilibria in the series of substituted 9-hydroxy-3-melhylphenalen-1-ones involve proton transfer from the hydroxy to the carbonyl group. The state of the equilibria is determined by the position of the methoxy groups. The relations between the heats of formation of tautomers, calculated by the AMI method, are consistent with the 1H and 13C NMR data.

Номер выпуска
3
Язык
Английский
Страницы
401-406
Статус
Опубликовано
Том
32
Год
1996
Организации
  • 1 Russ. Univ. of Peoples' Friendship, ul. M.-Maklaya 6, 117198 GSP Moscow, Russian Federation
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/829/