The [2+2+2] cycloaddition is an elegant, atom-efficient and group tolerant process for the synthesis of carbo-and heterocycles, mostly aromatic, involving the formation of several C-C bonds in a single step. Cyclotrimerisation is catalyzed by a variety of organometallic complexes, including more than 15 different metals. The aim of this tutorial review is to point out the most recent advances in this field and to encourage the use of this reaction enroute to complex molecules. After summarizing the most common catalysts and reaction conditions generally used, we survey the mechanistic features currently accepted for this reaction. Section 4 covers the scope of the different [2+2+2] cycloaddition versions starting with the cyclotrimerisation of three triple bonds, including nitriles, with especial emphasis on asymmetric reactions that create central, axial or planar chirality. Then, reactions that use double bonds are addressed. Finally, the most outstanding examples of natural products synthesis using [2+2+2] cycloadditions as a key step reported recently are shown.
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Boñaga, LVR
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Zhang, HC
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Zhang, HC
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Moretto, AF
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Moretto, AF
;
Ye, H
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Ye, H
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Gauthier, DA
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Gauthier, DA
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Li, J
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Li, J
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Leo, GC
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Leo, GC
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Maryanoff, BE
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
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Univ Paris 06, Chim Organ Lab, UMR 7611, Inst Chim Mol, F-75252 Paris 05, FranceUniv Paris 06, Chim Organ Lab, UMR 7611, Inst Chim Mol, F-75252 Paris 05, France
Phansavath, P
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Aubert, C
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Univ Paris 06, Chim Organ Lab, UMR 7611, Inst Chim Mol, F-75252 Paris 05, FranceUniv Paris 06, Chim Organ Lab, UMR 7611, Inst Chim Mol, F-75252 Paris 05, France
Aubert, C
;
Malacria, M
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Univ Paris 06, Chim Organ Lab, UMR 7611, Inst Chim Mol, F-75252 Paris 05, FranceUniv Paris 06, Chim Organ Lab, UMR 7611, Inst Chim Mol, F-75252 Paris 05, France
机构:
Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Boñaga, LVR
;
Zhang, HC
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Zhang, HC
;
Moretto, AF
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Moretto, AF
;
Ye, H
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Ye, H
;
Gauthier, DA
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Gauthier, DA
;
Li, J
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Li, J
;
Leo, GC
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Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
Leo, GC
;
Maryanoff, BE
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机构:
Johnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USAJohnson & Johnson Pharmaceut, Res & Dev, Drug Discovery, Spring House, PA 19477 USA
机构:
Univ Paris 06, Chim Organ Lab, UMR 7611, Inst Chim Mol, F-75252 Paris 05, FranceUniv Paris 06, Chim Organ Lab, UMR 7611, Inst Chim Mol, F-75252 Paris 05, France
Phansavath, P
;
Aubert, C
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h-index: 0
机构:
Univ Paris 06, Chim Organ Lab, UMR 7611, Inst Chim Mol, F-75252 Paris 05, FranceUniv Paris 06, Chim Organ Lab, UMR 7611, Inst Chim Mol, F-75252 Paris 05, France
Aubert, C
;
Malacria, M
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h-index: 0
机构:
Univ Paris 06, Chim Organ Lab, UMR 7611, Inst Chim Mol, F-75252 Paris 05, FranceUniv Paris 06, Chim Organ Lab, UMR 7611, Inst Chim Mol, F-75252 Paris 05, France