Transition Metal Catalyzed Cycloisomerizations of 1,n-Allenynes and -Allenenes

被引:554
作者
Aubert, Corinne [1 ]
Fensterbank, Louis [1 ]
Garcia, Pierre [1 ]
Malacria, Max [1 ]
Simonneau, Antoine [1 ]
机构
[1] Univ Paris 06, UPMC, Inst Parisien Chim Mol, CNRS,UMR 7201, F-75005 Paris, France
关键词
ALDER-ENE REACTION; C-H BOND; GOLD(I)-CATALYZED INTRAMOLECULAR HYDROARYLATION; COBALT(I)-MEDIATED 2+2+2 CYCLIZATION; INTERMOLECULAR 4+2 CYCLOADDITION; ASYMMETRIC TOTAL-SYNTHESIS; FORMAL COPE REARRANGEMENT; RING-CLOSING METATHESIS; FACE-SELECTIVE PLATINUM; PAUSON-KHAND REACTION;
D O I
10.1021/cr100376w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Advances on the transition metal catalyzed cycloisomerizations of 1,n-allenynes and 1,n-allenenes are summarized. Malacria reported the first transition metal-mediated isomerization of allenynes and Brummond proposed the formation of a rhodacyclopentene intermediate, which after β-H and reductive elimination gives the cross-conjugated triene. Hydroxylated 1,5 allenynes were explored by Malacria and Fensterbank in the context of gold and platinum catalysis. In 2008, Akita reported the gold(III)-catalyzed cycloisomerizations of 1-allenyl-1-ethynyl acetates into 4-methylene-2- cyclopentenones. Mascarenas reported the platinum and NHC-gold complexes catalyzed reaction of allenediene to give diastereoselectively 1,4-cycloheptadiene derivatives. The groups of Toste and Iwasawa independently reported respectively the gold- and platinum-catalyzed cyclization of vinylallenes.
引用
收藏
页码:1954 / 1993
页数:40
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