The unprecedented transformation of a sterically crowded cyclopalladated secondary benzylamine including (sp(3))C-C(sp(3)) bond activation under mild conditionsстатья
Информация о цитировании статьи получена из
Web of Science,
Scopus
Статья опубликована в журнале из списка Web of Science и/или Scopus
Дата последнего поиска статьи во внешних источниках: 18 июля 2013 г.
Аннотация:An unusual process of palladium mediated cleavage of an (sp3)C-C(sp3) bond between two non-activated carbon atoms in a sterically crowded secondary benzylamine is discovered. It includes the conversion of cyclopalladated N-methyl-alpha-tert-butylbenzylamine formed at the first stage into the ortho-palladated N-methylbenzylidenamine.