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For the use of sulfones possessing an acidic α-C-H bond see :(a) Fuchs, P. L.; Braish, T. F. Chem. Rev. 1986, 86, 903.
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12344296105
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A variety of transformations using sulfones lacking an acidic α-C-H bond have been reported, e.g., conjugate addition of Grignard reagents: (a) Julia, M.; Righini, A.; Verpeaux, J.-N. Tetrahedron 1979, 26, 2393.
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A variety of transformations using sulfones lacking an acidic α-C-H bond have been reported, e.g., conjugate addition of Grignard reagents: (a) Julia, M.; Righini, A.; Verpeaux, J.-N. Tetrahedron 1979, 26, 2393.
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(c) Plietker, B.; Dieskau, A.; Mows, K.; Jatsch, A. Angew. Chem., Int. Ed. 2008, 47, 198.
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33750950658
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Although not in the focus of the present study vinyl sulfones are imporant building blocks in medicinal chemistry, for a review see: Meadows, D. C, Gervay-Hague, J. Med. Res. Rev. 2006, 26, 793. Investigations on the scope of the allylic sulfonation, isomerization are currently being carried out in our laboratories
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Although not in the focus of the present study vinyl sulfones are imporant building blocks in medicinal chemistry, for a review see: Meadows, D. C.; Gervay-Hague, J. Med. Res. Rev. 2006, 26, 793. Investigations on the scope of the allylic sulfonation - isomerization are currently being carried out in our laboratories.
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A metal-by-metal displacement was observed in the related Rhcatalyzed allylic substitution: Wucher, B.; Moser, M.; Schumacher, S. A.; Rominger, F.; Kunz, D. Angew. Chem., Int. Ed. 2009, 48, 4417.
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A metal-by-metal displacement was observed in the related Rhcatalyzed allylic substitution: Wucher, B.; Moser, M.; Schumacher, S. A.; Rominger, F.; Kunz, D. Angew. Chem., Int. Ed. 2009, 48, 4417.
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