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Exo- and endo-palladacycles derived from (4R)-phenyl-2-oxazolinesстатья
Информация о цитировании статьи получена из
Web of Science,
Scopus
Дата последнего поиска статьи во внешних источниках: 25 декабря 2013 г.
- Авторы: Gorunova O.N., Keuseman K.J., Goebel B.M., Kataeva N.A., Churakov A.V., Kuz'mina L.G., Dunina V.V., Smoliakova I.P.
- Журнал: J.Organometallic Chemistry
- Том: 689
- Год издания: 2004
- Первая страница: 2382
- Последняя страница: 2394
- DOI: 10.1016/j.jorganchem.2004.04.029
- Аннотация: Two novel oxazoline-derived palladacycles bearing an endo- or exo-C=N bond were prepared by direct ortho-palladation of (R)-2,4-diphenyl- or (R)-2-methyl-4-phenyl-2-oxazolines, respectively. The structures of the palladacycles’ dimeric forms and corresponding mononuclear PPh3-derivatives were confirmed by IR, 1H, 13C and 2D NMR spectroscopy. An X-ray diffraction study of the l-chloro-dimeric cyclopalladated derivative of (R)-2,4-diphenyl-2-oxazoline proved the endo structure of the palladacycle.
- Добавил в систему: Дунина Валерия Владимировна