Gold-catalyzed cycloisomerization of 1,5-allenynes via dual activation of an ene reaction.
نویسندگان
چکیده
Tris(triphenylphosphinegold) oxonium tetrafluoroborate, [(Ph3PAu)3O]BF4, catalyzes the rearrangement of 1,5-allenynes to produce cross-conjugated trienes. Experimental and computational evidence shows that the ene reaction proceeds through a unique nucleophilic addition of an allene double bond to a cationic phosphinegold(I)-complexed phosphinegold(I) acetylide, followed by a 1,5-hydrogen shift.
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عنوان ژورنال:
- Journal of the American Chemical Society
دوره 130 13 شماره
صفحات -
تاریخ انتشار 2008