Gold-Catalyzed Synthesis of Dibenzopentalenes - Evidence for Gold Vinylidenes

被引:221
|
作者
Hashmi, A. Stephen K. [1 ]
Wieteck, Marcel [1 ]
Braun, Ingo [1 ]
Noesel, Pascal [1 ]
Jongbloed, Linda [1 ]
Rudolph, Matthias [1 ]
Rominger, Frank [1 ]
机构
[1] Heidelberg Univ, Inst Organ Chem, D-69120 Heidelberg, Germany
关键词
alkynes; dibenzopentalenes; digold compounds; extended p-systems; gold catalysis; gold vinylidenes; vinylgold intermediates; GOLD(I)-CATALYZED CYCLOISOMERIZATION; HYDRATIVE CARBOCYCLIZATION; ORGANOGOLD COMPOUNDS; TANDEM REACTIONS; CYCLIZATION; DERIVATIVES; 1,6-DIYNES; ACCESS; ALKYNE; REARRANGEMENT;
D O I
10.1002/adsc.201200086
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of easily accessible arene-1,2-diynes, bearing one aryl substituent on one of the alkynyl groups, is readily converted to dibenzopentalenes in good yields by gold(I) catalysts. The participation of gold acetylides could be proven by the direct conversion to the corresponding gem-diaurated dibenzopentalenes with a gold catalyst. From an experiment with a gold acetylide complex and stoichiometric amounts of the gold catalyst the corresponding gem-diaurated complex of a dibenzopentalene could be obtained and characterized by X-ray crystal structure analysis. Labelling studies with deuterated alkynes show the expected deuteration of the two remaining positions of the pentalene core. All this provides evidence for a dual activation mode of the reaction and gold(I) vinylidene complexes as intermediates of the catalytic cycle.
引用
收藏
页码:555 / 562
页数:8
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