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Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
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Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
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Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
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Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
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Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
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Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
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Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
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Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
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-
-
Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
-
(1992)
Liebigs Ann. Chem.
, pp. 51
-
-
Suzuki, K.1
Seebach, D.2
-
26
-
-
0026317489
-
-
Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
-
(1991)
Tetrahedron :Asymmetry
, vol.2
, pp. 1329
-
-
Annunziata, R.1
Cinquini, M.2
Cozzi, F.3
Raimondi, L.4
Pilati, T.5
-
27
-
-
0001439446
-
-
Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
-
(1993)
J.Org.Chem.
, vol.58
, pp. 4221
-
-
Tatsukawa, A.1
Dan, M.2
Ohbatake, M.3
Kawatake, K.4
Fukata, T.5
Wada, E.6
Kanemasa, S.7
Kakei, S.8
-
28
-
-
0029026897
-
-
Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
-
(1995)
Tetrahedron
, vol.57
, pp. 10463
-
-
Kanemasa, S.1
Nomura, M.2
Yoshinaga, S.3
Yamamoto, H.4
-
29
-
-
0028055289
-
-
Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 143
-
-
Kanemasa, S.1
Nomura, M.2
-
30
-
-
0025916976
-
-
Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
-
(1991)
Synthesis
, pp. 649
-
-
Duhamel, L.1
Duhamel, P.2
Enders, D.3
Karl, W.4
Leger, F.5
Poirier, J.M.6
Raabe, G.7
-
31
-
-
85085671625
-
-
Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
-
(1995)
Synthesis
, pp. 659
-
-
Enders, D.1
Kirchoff, J.2
Mannes, D.3
Raabe, G.4
-
32
-
-
84987319931
-
-
Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
-
(1992)
Synlett
, pp. 895
-
-
Enders, D.1
Karl, W.2
-
33
-
-
0030444826
-
-
and references therein
-
Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
-
(1996)
Synthesis
, pp. 1403
-
-
Enders, D.1
Klatt, M.2
-
34
-
-
0343211264
-
-
and references therein
-
Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
-
(1996)
Synlett
, pp. 827
-
-
Shimizu, M.1
Onogawa, Y.2
Fujisawa, T.3
-
35
-
-
33748912167
-
-
Numerous examples of enantioselective Michael additions of enolates and their synthetic equivalents that use chiral auxiliaries either on the donor or the acceptor have been reported. See, for instance: Perlmutter, P. in Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis, Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford, 1992; Oare, D.A.; Heathcock, C.H. Top.Stereochem. 1989, 19, 227-407. For some more recent examples see also: Schultz, A.G.; Lee, H. Tetrahedron Letters 1992, 33, 4397; Yamada, F.; Kozikoswki, A.P.; Reddy, E.R.; Pang, Y.-P.; Miller, J.H.; McKinney, M. J.Am.Chem.Soc. 1991, 113, 4695; Ouvrard, N.; Rodriguez, J.; Santelli, M. Angew.Chem.Int.Ed.Engl. 1992, 31, 1651; Hanessian, S.; Gomstyan, A. Tetrahedron Letters 1994, 35, 7509; Barluenga, J.; Montserrat, J.M.; Florez, J.; Garcia-Granda, S.; Martin, E. Chem.Eur .J . 1995, 1, 236; Yamazaki, T.; Haga, J.; Kitazume, T. Chem.Lett. 1991, 2175; Suzuki, K.; Seebach, D. Liebigs Ann. Chem. 1992, 51; Annunziata, R.; Cinquini, M.; Cozzi, F.; Raimondi, L.; Pilati, T. Tetrahedron :Asymmetry 1991, 2, 1329; Tatsukawa, A.; Dan, M.; Ohbatake, M.; Kawatake, K.; Fukata, T.; Wada, E.; Kanemasa, S.; Kakei, S. J.Org.Chem. 1993, 58, 4221; Kanemasa, S.; Nomura, M.; Yoshinaga, S.; Yamamoto, H. Tetrahedron 1995, 57, 10463; Kanemasa, S.; Nomura, M. Tetrahedron Lett. 1994, 35, 143; Duhamel, L.; Duhamel, P.; Enders, D.; Karl, W.; Leger, F.; Poirier, J.M.; Raabe, G. Synthesis 1991, 649; Enders, D.; Kirchoff, J.; Mannes, D.; Raabe, G. Synthesis 1995, 659; Enders, D.; Karl, W. Synlett 1992, 895; Enders D., Klatt M. Synthesis 1996, 1403 and references therein; Shimizu, M.; Onogawa, Y.; Fujisawa, T. Synlett 1996, 827 and references therein; Angert H. Czerwonka R. Reissig HU. Liebigs Ann. Chem. 1996, 259.
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0343210669
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note
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2occurs in Ih at -78°C to give 45% of the addition product.
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88
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0343646125
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2 is stable for Ih at -78°C, and 21 appears only after the addition of 2b to the mixture
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90
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0343210667
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note
-
Although the configuration of these compounds was not rigorously established they are likely to be the cis and trans isomers on the cyclopentenone ring, since the reaction of 19 with the acetate equivalent 2a also gives two isomers in 6:1 ratio.
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91
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0342775937
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note
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13C NMR analysis of the resulting glutarates: Bandiera, P. Tesi di Laurea, Universita' di Milano a.a. 1994-95.
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92
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For a discussion on the relative basicity of various carbonyl compounds in Diels-Alder reactions see: Hunt, I.R.; Rogers, C.; Woo, S.; Rauk, A.; Keay, B.A. J.Am.Chem.Soc. 1995, 117, 1049-1056; Rauk, A.; Hunt, I.R.; Keay, B.A. J.Org.Chem. 1994, 59, 6808-6816.
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For a discussion on the relative basicity of various carbonyl compounds in Diels-Alder reactions see: Hunt, I.R.; Rogers, C.; Woo, S.; Rauk, A.; Keay, B.A. J.Am.Chem.Soc. 1995, 117, 1049-1056; Rauk, A.; Hunt, I.R.; Keay, B.A. J.Org.Chem. 1994, 59, 6808-6816.
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0343210665
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note
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2 in the presence of 1 equiv of DIPEA, or filtering off the molecular sieves immediately after the formation of the Ti TADDOLate. In both cases the e.e. of the product was unaffected.
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96
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0343210664
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note
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TBDMSOTf is a good promoter for the addition of 2b to 1b: see ref. 10b .
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-
-
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101
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0342341002
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note
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Substrate 18 was chosen for these studies because of its higher stability compared to 1b.
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102
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0342341000
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note
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1H-NMR spectroscopy: Prof. DiMare, University of California at Santa Barbara, unpublished results, personal communication
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b) Sarko, C.R.; DiMare, M. unpublished results, private communication.
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0000036220
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