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For the cyclization of α-diazo-α-aryl ketones with an alkene tether between the ketone and the target C-H, see: (a) Fernández-Mateos, T. A, Pascual, Coca, G, Pérez Alonso, J. J, Rubio González, R, Simmonds, M. S. J, Blaney, W. M. Tetrahedron 1988, 54, 14989
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For the cyclization of α-diazo-α-aryl ketones with an alkene tether between the ketone and the target C-H, see: (a) Fernández-Mateos, T. A.; Pascual, Coca, G.; Pérez Alonso, J. J.; Rubio González, R.; Simmonds, M. S. J.; Blaney, W. M. Tetrahedron 1988, 54, 14989.
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28
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Several general methods have been developed for the preparation of α-aryl ketones. For example: (a) Abramovitch, R. A.; Barton, D. H. R.; Finet, J. P. Tetrahedron 1988, 44, 3039.
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Several general methods have been developed for the preparation of α-aryl ketones. For example: (a) Abramovitch, R. A.; Barton, D. H. R.; Finet, J. P. Tetrahedron 1988, 44, 3039.
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Several of the substances reported here were previously described. (a) 1a: Taber, D. F.; Tian, W. J. Am. Chem. Soc. 2006, 128, 1058.
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Several of the substances reported here were previously described. (a) 1a: Taber, D. F.; Tian, W. J. Am. Chem. Soc. 2006, 128, 1058.
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(b) 1b: Utimoto, K.; Takai, K. NATO AS1 Series, Series, C 1989, 269, 379.
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2b: ref. 9b
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34247596924
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13C multiplicities were determined with the aid of a JVERT pulse sequence, differentiating the signals for methyl and methine carbons as d and for methylene and quaternary carbons as u.
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13C multiplicities were determined with the aid of a JVERT pulse sequence, differentiating the signals for methyl and methine carbons as "d" and for methylene and quaternary carbons as "u".
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