Gold-Catalyzed Cycloisomerization of 1,5-Allenynes via Dual Activation of an Ene Reaction
摘要:
Tris(triphenylphosphinegold) oxonium tetrafluoroborate, [(Ph(3)PAU)(3)O]BF(4), 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 14 a cationic phosphinegold(l)-complexed phosphinegold(l) acetylide, followed by a 1,5-hydrogen shift.
Gold-Catalyzed Cycloisomerization of 1,5-Allenynes via Dual Activation of an Ene Reaction
作者:Paul Ha-Yeon Cheong、Philip Morganelli、Michael R. Luzung、K. N. Houk、F. Dean Toste
DOI:10.1021/ja711058f
日期:2008.4.1
Tris(triphenylphosphinegold) oxonium tetrafluoroborate, [(Ph(3)PAU)(3)O]BF(4), 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 14 a cationic phosphinegold(l)-complexed phosphinegold(l) acetylide, followed by a 1,5-hydrogen shift.