Synthetic Applications of the Nickel-Catalyzed Cyclization of Alkynes Combined with Addition Reactions in a Domino Process

被引:40
作者
Durandetti, Muriel [1 ,2 ,3 ]
Hardou, Lucie [1 ,2 ,3 ]
Lhermet, Rudy [1 ,2 ,3 ]
Rouen, Mathieu [1 ,2 ,3 ]
Maddaluno, Jacques [1 ,2 ,3 ]
机构
[1] Univ Rouen, CNRS UMR 6014, IRCOF, Lab Fonct Azotees & Oxygenees Complexes, F-76821 Mont St Aignan, France
[2] Univ Rouen, FR 3038, F-76821 Mont St Aignan, France
[3] INSA Rouen, F-76821 Mont St Aignan, France
关键词
alkynes; carbonickelation; domino reactions; nickel; vinylnickel; CROSS-COUPLING REACTIONS; ARYL HALIDES; STEREOSELECTIVE-SYNTHESIS; RADICAL CYCLIZATION; GRIGNARD-REAGENTS; INTRAMOLECULAR CARBOLITHIATION; EFFICIENT SYNTHESIS; VINYL HALIDES; BENZOFURANS; CHLORIDES;
D O I
10.1002/chem.201100967
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbonickelations of alkynes and functionalization of the resulting vinylnickel moiety have been performed efficiently in a nickel-catalyzed domino cyclization-condensation process. This reaction, which does not require the preparation of any other organometallic reagent, proceeds only by exo-dig cyclization. This convenient and mild method constitutes a one-pot synthesis of substituted dihydrobenzofurans, chromans, isochromans, indoles, or indanes. Theses valuable products are generally obtained in good yields and high stereoselectivity. They are shown to be useful synthons for rapid access to functionalized polycyclic skeletons.
引用
收藏
页码:12773 / 12783
页数:11
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