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Volumn 53, Issue 38, 1997, Pages 13009-13026

Enantioselective conjugate additions of silylketene acetals to 2-carboxycyclopentenones promoted by chiral Ti complexes

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPENTENONE DERIVATIVE;

EID: 0030768261     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00825-9     Document Type: Article
Times cited : (58)

References (112)
  • 5
    • 0025854912 scopus 로고
    • Otera, J.; Wakahara, Y.; Kamei, H.; Sato, T.; Nosaki, H.; Fukuzumi, S. Tetrahedron Lett. 1991, 32, 2405-2408; Mikami, K.; Terada, M.; Nakai, T. J.Org.Chem. 1991, 56, 5456-5459; Kobayashi, S.; Hachiya, I.; Takahori, T.; Araki, M.; Ishitani, H. Tetrahedron Lett. 1992, 33, 6815-6818; DuBay, W.J.; Grieco, P.A.; Todd, L.J. J.Org.Chem. 1994, 59, 6898-6899.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 2405-2408
    • Otera, J.1    Wakahara, Y.2    Kamei, H.3    Sato, T.4    Nosaki, H.5    Fukuzumi, S.6
  • 6
    • 33751499216 scopus 로고
    • Otera, J.; Wakahara, Y.; Kamei, H.; Sato, T.; Nosaki, H.; Fukuzumi, S. Tetrahedron Lett. 1991, 32, 2405-2408; Mikami, K.; Terada, M.; Nakai, T. J.Org.Chem. 1991, 56, 5456-5459; Kobayashi, S.; Hachiya, I.; Takahori, T.; Araki, M.; Ishitani, H. Tetrahedron Lett. 1992, 33, 6815-6818; DuBay, W.J.; Grieco, P.A.; Todd, L.J. J.Org.Chem. 1994, 59, 6898-6899.
    • (1991) J.Org.Chem. , vol.56 , pp. 5456-5459
    • Mikami, K.1    Terada, M.2    Nakai, T.3
  • 7
    • 0026486293 scopus 로고
    • Otera, J.; Wakahara, Y.; Kamei, H.; Sato, T.; Nosaki, H.; Fukuzumi, S. Tetrahedron Lett. 1991, 32, 2405-2408; Mikami, K.; Terada, M.; Nakai, T. J.Org.Chem. 1991, 56, 5456-5459; Kobayashi, S.; Hachiya, I.; Takahori, T.; Araki, M.; Ishitani, H. Tetrahedron Lett. 1992, 33, 6815-6818; DuBay, W.J.; Grieco, P.A.; Todd, L.J. J.Org.Chem. 1994, 59, 6898-6899.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 6815-6818
    • Kobayashi, S.1    Hachiya, I.2    Takahori, T.3    Araki, M.4    Ishitani, H.5
  • 8
    • 0001332793 scopus 로고
    • Otera, J.; Wakahara, Y.; Kamei, H.; Sato, T.; Nosaki, H.; Fukuzumi, S. Tetrahedron Lett. 1991, 32, 2405-2408; Mikami, K.; Terada, M.; Nakai, T. J.Org.Chem. 1991, 56, 5456-5459; Kobayashi, S.; Hachiya, I.; Takahori, T.; Araki, M.; Ishitani, H. Tetrahedron Lett. 1992, 33, 6815-6818; DuBay, W.J.; Grieco, P.A.; Todd, L.J. J.Org.Chem. 1994, 59, 6898-6899.
    • (1994) J.Org.Chem. , vol.59 , pp. 6898-6899
    • DuBay, W.J.1    Grieco, P.A.2    Todd, L.J.3
  • 17
    • 0004218246 scopus 로고
    • Ed. Baldwin, J.E., FRS & Magnus, P.D., FRS, Pergamon Press: Oxford
    • 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) Tetrahedron Organic Chemistry Series. Vol. 9: Conjugate Addition Reactions in Organic Synthesis , vol.9
    • Perlmutter, P.1
  • 18
    • 85050326125 scopus 로고
    • 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.
    • (1989) Top.Stereochem. , vol.19 , pp. 227-407
    • Oare, D.A.1    Heathcock, C.H.2
  • 19
    • 0026692815 scopus 로고
    • 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) Tetrahedron Letters , vol.33 , pp. 4397
    • Schultz, A.G.1    Lee, H.2
  • 20
    • 0025777337 scopus 로고
    • 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) J.Am.Chem.Soc. , vol.113 , pp. 4695
    • Yamada, F.1    Kozikoswki, A.P.2    Reddy, E.R.3    Pang, Y.-P.4    Miller, J.H.5    McKinney, M.6
  • 21
    • 33748242344 scopus 로고
    • 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) Angew.Chem.Int.Ed.Engl. , vol.31 , pp. 1651
    • Ouvrard, N.1    Rodriguez, J.2    Santelli, M.3
  • 22
    • 0028073786 scopus 로고
    • 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 Letters , vol.35 , pp. 7509
    • Hanessian, S.1    Gomstyan, A.2
  • 23
    • 84989530386 scopus 로고
    • 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) Chem.eur .J . , vol.1 , pp. 236
    • Barluenga, J.1    Montserrat, J.M.2    Florez, J.3    Garcia-Granda, S.4    Martin, E.5
  • 24
    • 0003112096 scopus 로고
    • 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) Chem.Lett. , pp. 2175
    • Yamazaki, T.1    Haga, J.2    Kitazume, T.3
  • 25
    • 84986685629 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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) Liebigs Ann. Chem. , pp. 259
    • Angert, H.1    Czerwonka, R.2    Reissig, H.U.3
  • 36
    • 49649133588 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986,51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1975) Tetrahedron Lett. , vol.16 , pp. 4057-4060
    • Wynberg, H.1    Helder, R.2
  • 37
    • 0000688857 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1979) J.Org.Chem. , vol.44 , pp. 2238-2244
    • Herman, K.1    Wynberg, H.2
  • 38
    • 0000867232 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1986) J.Org.Chem. , vol.51 , pp. 4710
    • Conn, R.S.E.1    Lovell, A.V.2    Karady, S.3    Weinstock, L.M.4
  • 39
    • 0001086513 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1987) Bull.Chem.Soc.Jpn. , vol.60 , pp. 4121
    • Inagaki, M.1    Hiratake, J.2    Yamamoto, Y.3    Oda, J.4
  • 40
    • 84985507254 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1984) Angew.Chem. Int.Ed.Engl. , vol.23 , pp. 312-313
    • Brünner, H.1    Hammer, B.2
  • 41
    • 0001236767 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1990) Tetrahedron , vol.46 , pp. 2927-2934
    • Desirnoni, G.1    Quadrelli, P.2    Righetti, P.P.3
  • 42
    • 0026156344 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1991) J.Mol.Catal. , vol.66 , pp. 7-21
    • Botteghi, C.1    Schionato, A.2    Boga, C.3    Fava, A.4
  • 43
    • 37049104245 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1981) J.Chem.Soc.Chem.Commun. , pp. 625-628
    • Cram, D.J.1    Sogah, G.D.Y.2
  • 44
    • 0000277569 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1986) Tetrahedron Lett. , vol.27 , pp. 3551-3554
    • Alonso-Lòpez, M.1    Martin-Lomas, M.2    Penadés, S.3
  • 45
    • 0011429737 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1988) Tetrahedron , vol.44 , pp. 1535-1543
    • Alonso-Lòpez, M.1    Jimenez-Barbero, J.2    Martin-Lomas, M.3    Penadés, S.4
  • 46
    • 0000860118 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 6943-6946
    • Takasu, M.1    Wakabayashi, H.2    Furuta, K.3    Yamamoto, H.4
  • 47
    • 0024843407 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 7229-7230
    • Aoki, S.1    Sasaki, S.2    Koga, K.3
  • 48
    • 0001414167 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1992) Heterocycles , vol.33 , pp. 493-495
    • Aoki, S.1    Sasaki, S.2    Koga, K.3
  • 49
    • 0027980834 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M.
    • (1994) Tetrahedron Asymm. , vol.5 , pp. 1431
    • Kumamoto, T.1    Aoki, S.2    Nakajima, M.3    Koga, K.4
  • 50
    • 33748247624 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1993) Angew.Chem. Int.Ed.Engl. , vol.32 , pp. 1176-1178
    • Yamaguchi, M.1    Shiraishi, T.2    Hirama, M.3
  • 51
    • 0027993384 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 8233-8236
    • Yamaguchi, M.1    Shiraishi, T.2    Igarashi, Y.3    Hirama, M.4
  • 52
    • 0027943133 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1994) Tetrahedron Lett. , vol.55 , pp. 8805-8808
    • Kawara, A.1    Taguci, T.2
  • 53
    • 0028377975 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1994) J.Am.Chem.Soc. , vol.116 , pp. 1571-1572
    • Sasai, H.1    Arai, T.2    Shibasaki, M.3
  • 54
    • 11944252146 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1995) J.Am.Chem.Soc. , vol.117 , pp. 6194-6198
    • Sasai, H.1    Arai, T.2    Satow, Y.3    Houk, K.N.4    Shibasaki, M.5
  • 55
    • 0028302405 scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1994) Tetrahedron , vol.50 , pp. 4439-4454
    • Sawamura, M.1    Hamashima, H.2    Ito, Y.3
  • 56
    • 0030605817 scopus 로고    scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 5561-5564
    • Sasai, H.1    Emori, E.2    Arai, T.3    Shibasaki, M.4
  • 57
    • 33748240969 scopus 로고    scopus 로고
    • Wynberg, H.; Helder, R. Tetrahedron Lett. 1975, 16, 4057-4060; Herman, K.; Wynberg, H. J.Org.Chem. 1979, 44, 2238-2244; Conn, R.S.E., Lovell, A.V.; Karady, S.; Weinstock, L.M. J.Org.Chem. 1986, 51,4710; Inagaki, M.; Hiratake, J.; Yamamoto, Y.; Oda, J. Bull.Chem.Soc.Jpn. 1987, 60, 4121; Brünner, H.; Hammer, B. Angew.Chem. Int.Ed.Engl. 1984, 23, 312-313; Desirnoni, G.; Quadrelli, P.; Righetti, P.P. Tetrahedron 1990, 46, 2927-2934; Botteghi, C.; Schionato, A.; Boga, C., Fava, A. J.Mol.Catal. 1991, 66, 7-21; Cram, D.J.; Sogah, G.D.Y. J.Chem.Soc.Chem.Commun. 1981, 625-628; Alonso-Lòpez, M.; Martin-Lomas M.; Penadés, S. Tetrahedron Lett. 1986, 27, 3551-3554; Alonso-Lòpez, M.; Jimenez-Barbero, J.; Martin-Lomas, M.; Penadés, S. Tetrahedron 1988, 44, 1535-1543; Takasu, M.; Wakabayashi, H.; Furuta, K.; Yamamoto, H. Tetrahedron Lett. 1988, 29, 6943-6946; Aoki, S.; Sasaki, S.; Koga, K. Tetrahedron Lett. 1989, 30, 7229-7230; Aoki, S.; Sasaki, S.; Koga, K. Heterocycles 1992, 33, 493-495; Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Tetrahedron Asymm. 1994, 5, 1431; Yamaguchi, M.; Shiraishi, T.; Hirama, M. Angew.Chem. Int.Ed.Engl. 1993, 32, 1176-1178; Yamaguchi, M.; Shiraishi, T.; Igarashi, Y.; Hirama, M. Tetrahedron Lett. 1994, 35, 8233-8236; Kawara, A.; Taguci, T. Tetrahedron Lett. 1994, 55, 8805-8808; Sasai, H.; Arai, T.; Shibasaki, M. J.Am.Chem.Soc. 1994, 116, 1571-1572; Sasai, H.; Arai, T.; Satow, Y.; Houk, K.N.; Shibasaki, M. J.Am.Chem.Soc. 1995, 117, 6194-6198; Sawamura, M.; Hamashima, H.; Ito, Y. Tetrahedron 1994, 50, 4439-4454; Sasai, H.; Emori, E.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1996, 37, 5561-5564; Arai, T.; Sasai, H.; Aoe, K.; Okamura, K.; Date, T.; Shibasaki, M. Angew.Chem.Int.Ed, Engl 1996, 35, 104.
    • (1996) Angew.Chem.Int.Ed, Engl , vol.35 , pp. 104
    • Arai, T.1    Sasai, H.2    Aoe, K.3    Okamura, K.4    Date, T.5    Shibasaki, M.6
  • 64
    • 33845283322 scopus 로고
    • Loncharich, R.J.; Schwartz, R.T.; Houk, K.N. J.Am.Chem.Soc. 1987, 709, 14-23; Ruiz-Lopez, M.F.; Assfeld, X.; García, J.I.; Mayoral,. J.A.; Salvatella, L. J.Am.Chem.Soc. 1993, 115, 8780-8787; Chamberlin, R.A.; Reich, S.H. J.Am.Chem.Soc. 1985, 107, 1440-1441; Shida, N.; Kabuto, C.; Niwa, T.; Ebata, T.; Yamamoto, Y. J.Org.Chem. 1994,59, 4068-4075; Gung, B.W. Yanik, M.M. J.Org.Chem. 1996, 67, 947.
    • (1987) J.Am.Chem.Soc. , vol.709 , pp. 14-23
    • Loncharich, R.J.1    Schwartz, R.T.2    Houk, K.N.3
  • 65
    • 0001431384 scopus 로고
    • Loncharich, R.J.; Schwartz, R.T.; Houk, K.N. J.Am.Chem.Soc. 1987, 709, 14-23; Ruiz-Lopez, M.F.; Assfeld, X.; García, J.I.; Mayoral,. J.A.; Salvatella, L. J.Am.Chem.Soc. 1993, 115, 8780-8787; Chamberlin, R.A.; Reich, S.H. J.Am.Chem.Soc. 1985, 107, 1440-1441; Shida, N.; Kabuto, C.; Niwa, T.; Ebata, T.; Yamamoto, Y. J.Org.Chem. 1994,59, 4068-4075; Gung, B.W. Yanik, M.M. J.Org.Chem. 1996, 67, 947.
    • (1993) J.Am.Chem.Soc. , vol.115 , pp. 8780-8787
    • Ruiz-Lopez, M.F.1    Assfeld, X.2    García, J.I.3    Mayoral, J.A.4    Salvatella, L.5
  • 66
    • 0001030975 scopus 로고
    • Loncharich, R.J.; Schwartz, R.T.; Houk, K.N. J.Am.Chem.Soc. 1987, 709, 14-23; Ruiz-Lopez, M.F.; Assfeld, X.; García, J.I.; Mayoral,. J.A.; Salvatella, L. J.Am.Chem.Soc. 1993, 115, 8780-8787; Chamberlin, R.A.; Reich, S.H. J.Am.Chem.Soc. 1985, 107, 1440-1441; Shida, N.; Kabuto, C.; Niwa, T.; Ebata, T.; Yamamoto, Y. J.Org.Chem. 1994,59, 4068-4075; Gung, B.W. Yanik, M.M. J.Org.Chem. 1996, 67, 947.
    • (1985) J.Am.Chem.Soc. , vol.107 , pp. 1440-1441
    • Chamberlin, R.A.1    Reich, S.H.2
  • 67
    • 0000765196 scopus 로고
    • Loncharich, R.J.; Schwartz, R.T.; Houk, K.N. J.Am.Chem.Soc. 1987, 709, 14-23; Ruiz-Lopez, M.F.; Assfeld, X.; García, J.I.; Mayoral,. J.A.; Salvatella, L. J.Am.Chem.Soc. 1993, 115, 8780-8787; Chamberlin, R.A.; Reich, S.H. J.Am.Chem.Soc. 1985, 107, 1440-1441; Shida, N.; Kabuto, C.; Niwa, T.; Ebata, T.; Yamamoto, Y. J.Org.Chem. 1994,59, 4068-4075; Gung, B.W. Yanik, M.M. J.Org.Chem. 1996, 67, 947.
    • (1994) J.Org.Chem. , vol.59 , pp. 4068-4075
    • Shida, N.1    Kabuto, C.2    Niwa, T.3    Ebata, T.4    Yamamoto, Y.5
  • 68
    • 0000363586 scopus 로고    scopus 로고
    • Loncharich, R.J.; Schwartz, R.T.; Houk, K.N. J.Am.Chem.Soc. 1987, 709, 14-23; Ruiz-Lopez, M.F.; Assfeld, X.; García, J.I.; Mayoral,. J.A.; Salvatella, L. J.Am.Chem.Soc. 1993, 115, 8780-8787; Chamberlin, R.A.; Reich, S.H. J.Am.Chem.Soc. 1985, 107, 1440-1441; Shida, N.; Kabuto, C.; Niwa, T.; Ebata, T.; Yamamoto, Y. J.Org.Chem. 1994,59, 4068-4075; Gung, B.W. Yanik, M.M. J.Org.Chem. 1996, 67, 947.
    • (1996) J.Org.Chem. , vol.67 , pp. 947
    • Gung, B.W.1    Yanik, M.M.2
  • 72
    • 0000244225 scopus 로고
    • Ireland, R.E.; Mueller, R.H.; Williard, A.K. J.Am.Chem.Soc. 1976, 95, 2868; Evans, D.A.; McGee, L.R. Tetrahedron Lett. 1980, 21, 3975.
    • (1980) Tetrahedron Lett. , vol.21 , pp. 3975
    • Evans, D.A.1    McGee, L.R.2
  • 73
    • 0000389195 scopus 로고
    • Seebach, D.; Plattner, D.A.; Beck, A.K.; Wang, Y.M.; Hunziker, D.Helv.Chim.Acta 1992, 75, 2171; Beck, A.K.; Bastani, B.; Plattner, D.A.; Petter, W.; Seebach, D.; Braun Schweiger, H.; Gysi, P.; La Vecchia, L. Chimia 1991, 45, 238; Seebach, D.; Beck, A.K.; Imwinkelried, R.; Roggo, S.; Wonnacott, A. Helv.Chim.Acta 1987, 70, 954; Weber, E.; Dorpinghaus, N.; Golberg, I. J.Chem.Soc.Chem.Commun. 1988, 1566; Irurre, J.; Alonso-Alija, C.; Piniella, J.F.; Alvarez-Larena, A. Tetrahedron:Asymmetry 1992, 3, 1591; Bussche-Hunnefeld, Ch.v.d.; Beck, A.K.; Lengweiler, U.; Seebach, D. Helv.Chim.Acta 1992, 75, 438.
    • (1992) Helv.Chim.Acta , vol.75 , pp. 2171
    • Seebach, D.1    Plattner, D.A.2    Beck, A.K.3    Wang, Y.M.4    Hunziker, D.5
  • 74
    • 0001570290 scopus 로고
    • Seebach, D.; Plattner, D.A.; Beck, A.K.; Wang, Y.M.; Hunziker, D.Helv.Chim.Acta 1992, 75, 2171; Beck, A.K.; Bastani, B.; Plattner, D.A.; Petter, W.; Seebach, D.; Braun Schweiger, H.; Gysi, P.; La Vecchia, L. Chimia 1991, 45, 238; Seebach, D.; Beck, A.K.; Imwinkelried, R.; Roggo, S.; Wonnacott, A. Helv.Chim.Acta 1987, 70, 954; Weber, E.; Dorpinghaus, N.; Golberg, I. J.Chem.Soc.Chem.Commun. 1988, 1566; Irurre, J.; Alonso-Alija, C.; Piniella, J.F.; Alvarez-Larena, A. Tetrahedron:Asymmetry 1992, 3, 1591; Bussche-Hunnefeld, Ch.v.d.; Beck, A.K.; Lengweiler, U.; Seebach, D. Helv.Chim.Acta 1992, 75, 438.
    • (1991) Chimia , vol.45 , pp. 238
    • Beck, A.K.1    Bastani, B.2    Plattner, D.A.3    Petter, W.4    Seebach, D.5    Braun Schweiger, H.6    Gysi, P.7    La Vecchia, L.8
  • 75
    • 84987490954 scopus 로고
    • Seebach, D.; Plattner, D.A.; Beck, A.K.; Wang, Y.M.; Hunziker, D.Helv.Chim.Acta 1992, 75, 2171; Beck, A.K.; Bastani, B.; Plattner, D.A.; Petter, W.; Seebach, D.; Braun Schweiger, H.; Gysi, P.; La Vecchia, L. Chimia 1991, 45, 238; Seebach, D.; Beck, A.K.; Imwinkelried, R.; Roggo, S.; Wonnacott, A. Helv.Chim.Acta 1987, 70, 954; Weber, E.; Dorpinghaus, N.; Golberg, I. J.Chem.Soc.Chem.Commun. 1988, 1566; Irurre, J.; Alonso-Alija, C.; Piniella, J.F.; Alvarez-Larena, A. Tetrahedron:Asymmetry 1992, 3, 1591; Bussche-Hunnefeld, Ch.v.d.; Beck, A.K.; Lengweiler, U.; Seebach, D. Helv.Chim.Acta 1992, 75, 438.
    • (1987) Helv.Chim.Acta , vol.70 , pp. 954
    • Seebach, D.1    Beck, A.K.2    Imwinkelried, R.3    Roggo, S.4    Wonnacott, A.5
  • 76
    • 37049089854 scopus 로고
    • Seebach, D.; Plattner, D.A.; Beck, A.K.; Wang, Y.M.; Hunziker, D.Helv.Chim.Acta 1992, 75, 2171; Beck, A.K.; Bastani, B.; Plattner, D.A.; Petter, W.; Seebach, D.; Braun Schweiger, H.; Gysi, P.; La Vecchia, L. Chimia 1991, 45, 238; Seebach, D.; Beck, A.K.; Imwinkelried, R.; Roggo, S.; Wonnacott, A. Helv.Chim.Acta 1987, 70, 954; Weber, E.; Dorpinghaus, N.; Golberg, I. J.Chem.Soc.Chem.Commun. 1988, 1566; Irurre, J.; Alonso-Alija, C.; Piniella, J.F.; Alvarez-Larena, A. Tetrahedron:Asymmetry 1992, 3, 1591; Bussche-Hunnefeld, Ch.v.d.; Beck, A.K.; Lengweiler, U.; Seebach, D. Helv.Chim.Acta 1992, 75, 438.
    • (1988) J.Chem.Soc.Chem.Commun. , pp. 1566
    • Weber, E.1    Dorpinghaus, N.2    Golberg, I.3
  • 77
    • 0026619595 scopus 로고
    • Seebach, D.; Plattner, D.A.; Beck, A.K.; Wang, Y.M.; Hunziker, D.Helv.Chim.Acta 1992, 75, 2171; Beck, A.K.; Bastani, B.; Plattner, D.A.; Petter, W.; Seebach, D.; Braun Schweiger, H.; Gysi, P.; La Vecchia, L. Chimia 1991, 45, 238; Seebach, D.; Beck, A.K.; Imwinkelried, R.; Roggo, S.; Wonnacott, A. Helv.Chim.Acta 1987, 70, 954; Weber, E.; Dorpinghaus, N.; Golberg, I. J.Chem.Soc.Chem.Commun. 1988, 1566; Irurre, J.; Alonso-Alija, C.; Piniella, J.F.; Alvarez-Larena, A. Tetrahedron:Asymmetry 1992, 3, 1591; Bussche-Hunnefeld, Ch.v.d.; Beck, A.K.; Lengweiler, U.; Seebach, D. Helv.Chim.Acta 1992, 75, 438.
    • (1992) Tetrahedron:Asymmetry , vol.3 , pp. 1591
    • Irurre, J.1    Alonso-Alija, C.2    Piniella, J.F.3    Alvarez-Larena, A.4
  • 78
    • 84987346056 scopus 로고
    • Seebach, D.; Plattner, D.A.; Beck, A.K.; Wang, Y.M.; Hunziker, D.Helv.Chim.Acta 1992, 75, 2171; Beck, A.K.; Bastani, B.; Plattner, D.A.; Petter, W.; Seebach, D.; Braun Schweiger, H.; Gysi, P.; La Vecchia, L. Chimia 1991, 45, 238; Seebach, D.; Beck, A.K.; Imwinkelried, R.; Roggo, S.; Wonnacott, A. Helv.Chim.Acta 1987, 70, 954; Weber, E.; Dorpinghaus, N.; Golberg, I. J.Chem.Soc.Chem.Commun. 1988, 1566; Irurre, J.; Alonso-Alija, C.; Piniella, J.F.; Alvarez-Larena, A. Tetrahedron:Asymmetry 1992, 3, 1591; Bussche-Hunnefeld, Ch.v.d.; Beck, A.K.; Lengweiler, U.; Seebach, D. Helv.Chim.Acta 1992, 75, 438.
    • (1992) Helv.Chim.Acta , vol.75 , pp. 438
    • Bussche-Hunnefeld, Ch.V.D.1    Beck, A.K.2    Lengweiler, U.3    Seebach, D.4
  • 86
    • 0343210669 scopus 로고    scopus 로고
    • note
    • 2occurs in Ih at -78°C to give 45% of the addition product.
  • 89
    • 0343646125 scopus 로고    scopus 로고
    • note
    • 2 is stable for Ih at -78°C, and 21 appears only after the addition of 2b to the mixture
  • 90
    • 0343210667 scopus 로고    scopus 로고
    • 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.
  • 91
    • 0342775937 scopus 로고    scopus 로고
    • note
    • 13C NMR analysis of the resulting glutarates: Bandiera, P. Tesi di Laurea, Universita' di Milano a.a. 1994-95.
  • 92
    • 0000875294 scopus 로고
    • 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.
    • (1995) J.Am.Chem.Soc. , vol.117 , pp. 1049-1056
    • Hunt, I.R.1    Rogers, C.2    Woo, S.3    Rauk, A.4    Keay, B.A.5
  • 93
    • 33751157459 scopus 로고
    • 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.
    • (1994) J.Org.Chem. , vol.59 , pp. 6808-6816
    • Rauk, A.1    Hunt, I.R.2    Keay, B.A.3
  • 95
    • 0343210665 scopus 로고    scopus 로고
    • note
    • 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.
  • 96
    • 0343210664 scopus 로고    scopus 로고
    • note
    • TBDMSOTf is a good promoter for the addition of 2b to 1b: see ref. 10b .
  • 101
    • 0342341002 scopus 로고    scopus 로고
    • note
    • Substrate 18 was chosen for these studies because of its higher stability compared to 1b.
  • 102
    • 0342341000 scopus 로고    scopus 로고
    • note
    • 1H-NMR spectroscopy: Prof. DiMare, University of California at Santa Barbara, unpublished results, personal communication
  • 106
    • 0342340999 scopus 로고    scopus 로고
    • unpublished results, private communication
    • b) Sarko, C.R.; DiMare, M. unpublished results, private communication.
    • Sarko, C.R.1    DiMare, M.2
  • 108
    • 0000875294 scopus 로고
    • For a discussion of the relative basicity of carbonyl groups, see: Hunt, I.R.; Rogers, C.; Woo, S.; Rauk, A. ; Keay, B.A. J.Am.Chem.Soc. 1995, 117, 1049; Rauk, A.; Hunt, I.R.; Keay, B.A. J.Org.Chem. 1994, 59, 6808.
    • (1995) J.Am.Chem.Soc. , vol.117 , pp. 1049
    • Hunt, I.R.1    Rogers, C.2    Woo, S.3    Rauk, A.4    Keay, B.A.5
  • 109
    • 33751157459 scopus 로고
    • For a discussion of the relative basicity of carbonyl groups, see: Hunt, I.R.; Rogers, C.; Woo, S.; Rauk, A. ; Keay, B.A. J.Am.Chem.Soc. 1995, 117, 1049; Rauk, A.; Hunt, I.R.; Keay, B.A. J.Org.Chem. 1994, 59, 6808.
    • (1994) J.Org.Chem. , vol.59 , pp. 6808
    • Rauk, A.1    Hunt, I.R.2    Keay, B.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.