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For a review, see: Parenty, A.; Moreau, X.; Campagne, J. M. Chem. Rev. 2006, 106, 911.
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For a review, see: Fu, G. C. In Modern Rhodium-Catalyzed Reactions; Evans, P. A., Ed.; Wiley-VCH: New York, 2005; pp 79-91 and references therein.
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Fu, G.C.1
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To our knowledge, there are no other transition metal-catalyzed ketone hydroacylations. For Rh- and Ru-catalyzed aldehyde hydroacylation, see: a
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To our knowledge, there are no other transition metal-catalyzed ketone hydroacylations. For Rh- and Ru-catalyzed aldehyde hydroacylation, see: (a) Fuji, K.; Morimoto, T.; Tsutsumi K.; Kakiuchi, K. Chem. Commun. 2005, 3295.
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(a) Moxham, G. L.; Randell-Sly, H. E.; Brayshaw, S. K.; Woodward, R. L.; Weller, A. S.; Willis, M. C. Angew. Chem., Int. Ed. 2006, 45, 7618.
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(b) Mail, R. E.; Garralda, M. A.; Hernández, R.; Ibarlucea, L. Organomet. 2000, 19, 5310.
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(a) For a Tishchenko review, see: Mahrwald, R. Curr. Org. Chem. 2003, 7, 1713.
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For an asymmetric Tishchenko, see
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(b) For an asymmetric Tishchenko, see: Hsu, J. L.; Fang, J. M. J. Org. Chem. 2001, 66, 8573.
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Fang, J.M.2
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For reviews on the benzoin reaction, see: a
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For reviews on the benzoin reaction, see: (a) Ide, W. S.; Buck, J. S. Org. React. 1948, 4, 269.
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Org. React
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For enantioselective NHC-catalyzed benzoin reactions, see: a
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For enantioselective NHC-catalyzed benzoin reactions, see: (a) Takikawa, H.; Hachisu, Y.; Bode, J. W.; Suzuki, K. Angew. Chem., Int. Ed. 2006, 45, 3492.
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(b) Enders, D.; Niemeier, O.; Balensiefer, T. Angew. Chem., Int. Ed. 2006, 45, 1463.
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Enders, D.1
Niemeier, O.2
Balensiefer, T.3
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41449091301
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Chelation has been proposed to stabilize Rh(III)-acyl intermediates and suppress decarbonylation; see: (a) ref 5a.
-
Chelation has been proposed to stabilize Rh(III)-acyl intermediates and suppress decarbonylation; see: (a) ref 5a.
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19
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(b) Imai, M.; Tanaka, M.; Nagumo, S.; Kawahara, N.; Suemune, H. J. Org. Chem. 2007, 72, 2543.
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(c) Jun, C.-H.; Moon, C. W.; Lee, D.-Y. Chem. - Eur. J. 2002, 8, 2422 and references cited therein.
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