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Reviews, see: (a) Iwabuchi, Y.; Hatakeyama, S. J. Synth. Org. Chem. Jpn. 2002, 60, 2; (b) Ciganek, E. Org. React. 1997, 51, 201; (c) Drewes, S. E.; Roos, G. H. P. Tetrahedron, 1988, 44, 4653; (d) Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron, 1996, 52, 8001. Recently Iwabuchi and Hatakeyama et al. have reported an elegant catalytic asymmetric Baylis-Hillman reaction, see Iwabuchi, Y.; Nakatani, M.; Yokoyama, N.; Hatakeyama, S. J. Am. Chem. Soc. 1999, 121, 10219.
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(1988)
Tetrahedron
, vol.44
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Drewes, S.E.1
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Reviews, see: (a) Iwabuchi, Y.; Hatakeyama, S. J. Synth. Org. Chem. Jpn. 2002, 60, 2; (b) Ciganek, E. Org. React. 1997, 51, 201; (c) Drewes, S. E.; Roos, G. H. P. Tetrahedron, 1988, 44, 4653; (d) Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron, 1996, 52, 8001. Recently Iwabuchi and Hatakeyama et al. have reported an elegant catalytic asymmetric Baylis-Hillman reaction, see Iwabuchi, Y.; Nakatani, M.; Yokoyama, N.; Hatakeyama, S. J. Am. Chem. Soc. 1999, 121, 10219.
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(1996)
Tetrahedron
, vol.52
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Basavaiah, D.1
Rao, P.D.2
Hyma, R.S.3
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Reviews, see: (a) Iwabuchi, Y.; Hatakeyama, S. J. Synth. Org. Chem. Jpn. 2002, 60, 2; (b) Ciganek, E. Org. React. 1997, 51, 201; (c) Drewes, S. E.; Roos, G. H. P. Tetrahedron, 1988, 44, 4653; (d) Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron, 1996, 52, 8001. Recently Iwabuchi and Hatakeyama et al. have reported an elegant catalytic asymmetric Baylis-Hillman reaction, see Iwabuchi, Y.; Nakatani, M.; Yokoyama, N.; Hatakeyama, S. J. Am. Chem. Soc. 1999, 121, 10219.
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(1999)
J. Am. Chem. Soc.
, vol.121
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Iwabuchi, Y.1
Nakatani, M.2
Yokoyama, N.3
Hatakeyama, S.4
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Mukherjee, S.B.2
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Bhat, S.V.5
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Review, see: (a) Matsumoto, K.; Kaneko, M.; Katsura, H.; Hayashi, N.; Uchida, T.; Acheson, R. M. Heterocycles 1998, 47, 1135; (b) Ciobanu, M.; Matsumoto, K. Liebigs Ann. Recueil 1997, 623; (c) Matsumoto, K.; Sera, A.; Uchida, T. Synthesis, 1985, 1; (d) Matsumoto, K.; Sera, A. Synthesis 1985, 999; (e) Jenner, G. Tetrahedron 2002, 58, 5185; (f) Jenner, G. Tetrahedron 1997, 53, 2669; (g) Jenner, G. J. Phy. Org. Chem. 2002, 15, 1; (h) Giguere, R. J. In Organic Synthesis Theory and Applications; Hudlicky, T., Ed.; London: JAI Press Inc. 1989; Vol. 1.
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Matsumoto, K.1
Kaneko, M.2
Katsura, H.3
Hayashi, N.4
Uchida, T.5
Acheson, R.M.6
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Review, see: (a) Matsumoto, K.; Kaneko, M.; Katsura, H.; Hayashi, N.; Uchida, T.; Acheson, R. M. Heterocycles 1998, 47, 1135; (b) Ciobanu, M.; Matsumoto, K. Liebigs Ann. Recueil 1997, 623; (c) Matsumoto, K.; Sera, A.; Uchida, T. Synthesis, 1985, 1; (d) Matsumoto, K.; Sera, A. Synthesis 1985, 999; (e) Jenner, G. Tetrahedron 2002, 58, 5185; (f) Jenner, G. Tetrahedron 1997, 53, 2669; (g) Jenner, G. J. Phy. Org. Chem. 2002, 15, 1; (h) Giguere, R. J. In Organic Synthesis Theory and Applications; Hudlicky, T., Ed.; London: JAI Press Inc. 1989; Vol. 1.
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Liebigs Ann. Recueil
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Ciobanu, M.1
Matsumoto, K.2
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Review, see: (a) Matsumoto, K.; Kaneko, M.; Katsura, H.; Hayashi, N.; Uchida, T.; Acheson, R. M. Heterocycles 1998, 47, 1135; (b) Ciobanu, M.; Matsumoto, K. Liebigs Ann. Recueil 1997, 623; (c) Matsumoto, K.; Sera, A.; Uchida, T. Synthesis, 1985, 1; (d) Matsumoto, K.; Sera, A. Synthesis 1985, 999; (e) Jenner, G. Tetrahedron 2002, 58, 5185; (f) Jenner, G. Tetrahedron 1997, 53, 2669; (g) Jenner, G. J. Phy. Org. Chem. 2002, 15, 1; (h) Giguere, R. J. In Organic Synthesis Theory and Applications; Hudlicky, T., Ed.; London: JAI Press Inc. 1989; Vol. 1.
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(1985)
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Sera, A.2
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Review, see: (a) Matsumoto, K.; Kaneko, M.; Katsura, H.; Hayashi, N.; Uchida, T.; Acheson, R. M. Heterocycles 1998, 47, 1135; (b) Ciobanu, M.; Matsumoto, K. Liebigs Ann. Recueil 1997, 623; (c) Matsumoto, K.; Sera, A.; Uchida, T. Synthesis, 1985, 1; (d) Matsumoto, K.; Sera, A. Synthesis 1985, 999; (e) Jenner, G. Tetrahedron 2002, 58, 5185; (f) Jenner, G. Tetrahedron 1997, 53, 2669; (g) Jenner, G. J. Phy. Org. Chem. 2002, 15, 1; (h) Giguere, R. J. In Organic Synthesis Theory and Applications; Hudlicky, T., Ed.; London: JAI Press Inc. 1989; Vol. 1.
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(1985)
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Review, see: (a) Matsumoto, K.; Kaneko, M.; Katsura, H.; Hayashi, N.; Uchida, T.; Acheson, R. M. Heterocycles 1998, 47, 1135; (b) Ciobanu, M.; Matsumoto, K. Liebigs Ann. Recueil 1997, 623; (c) Matsumoto, K.; Sera, A.; Uchida, T. Synthesis, 1985, 1; (d) Matsumoto, K.; Sera, A. Synthesis 1985, 999; (e) Jenner, G. Tetrahedron 2002, 58, 5185; (f) Jenner, G. Tetrahedron 1997, 53, 2669; (g) Jenner, G. J. Phy. Org. Chem. 2002, 15, 1; (h) Giguere, R. J. In Organic Synthesis Theory and Applications; Hudlicky, T., Ed.; London: JAI Press Inc. 1989; Vol. 1.
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(2002)
Tetrahedron
, vol.58
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Jenner, G.1
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Review, see: (a) Matsumoto, K.; Kaneko, M.; Katsura, H.; Hayashi, N.; Uchida, T.; Acheson, R. M. Heterocycles 1998, 47, 1135; (b) Ciobanu, M.; Matsumoto, K. Liebigs Ann. Recueil 1997, 623; (c) Matsumoto, K.; Sera, A.; Uchida, T. Synthesis, 1985, 1; (d) Matsumoto, K.; Sera, A. Synthesis 1985, 999; (e) Jenner, G. Tetrahedron 2002, 58, 5185; (f) Jenner, G. Tetrahedron 1997, 53, 2669; (g) Jenner, G. J. Phy. Org. Chem. 2002, 15, 1; (h) Giguere, R. J. In Organic Synthesis Theory and Applications; Hudlicky, T., Ed.; London: JAI Press Inc. 1989; Vol. 1.
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(1997)
Tetrahedron
, vol.53
, pp. 2669
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Jenner, G.1
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Review, see: (a) Matsumoto, K.; Kaneko, M.; Katsura, H.; Hayashi, N.; Uchida, T.; Acheson, R. M. Heterocycles 1998, 47, 1135; (b) Ciobanu, M.; Matsumoto, K. Liebigs Ann. Recueil 1997, 623; (c) Matsumoto, K.; Sera, A.; Uchida, T. Synthesis, 1985, 1; (d) Matsumoto, K.; Sera, A. Synthesis 1985, 999; (e) Jenner, G. Tetrahedron 2002, 58, 5185; (f) Jenner, G. Tetrahedron 1997, 53, 2669; (g) Jenner, G. J. Phy. Org. Chem. 2002, 15, 1; (h) Giguere, R. J. In Organic Synthesis Theory and Applications; Hudlicky, T., Ed.; London: JAI Press Inc. 1989; Vol. 1.
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Review, see: (a) Matsumoto, K.; Kaneko, M.; Katsura, H.; Hayashi, N.; Uchida, T.; Acheson, R. M. Heterocycles 1998, 47, 1135; (b) Ciobanu, M.; Matsumoto, K. Liebigs Ann. Recueil 1997, 623; (c) Matsumoto, K.; Sera, A.; Uchida, T. Synthesis, 1985, 1; (d) Matsumoto, K.; Sera, A. Synthesis 1985, 999; (e) Jenner, G. Tetrahedron 2002, 58, 5185; (f) Jenner, G. Tetrahedron 1997, 53, 2669; (g) Jenner, G. J. Phy. Org. Chem. 2002, 15, 1; (h) Giguere, R. J. In Organic Synthesis Theory and Applications; Hudlicky, T., Ed.; London: JAI Press Inc. 1989; Vol. 1.
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(1989)
Organic Synthesis Theory and Applications
, vol.1
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Giguere, R.J.1
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Hayakawa et al. elegantly applied the high pressure induced by water-freezing to the inactivation of microorganisms, see Hayakawa, K.; Ueno, Y.; Kawamura, S.; Kato, T.; Hayashi, R. Appl. Microbiol. Biotechnol. 1998, 50, 415.
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(1998)
Appl. Microbiol. Biotechnol.
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Hayakawa, K.1
Ueno, Y.2
Kawamura, S.3
Kato, T.4
Hayashi, R.5
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32
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0011186169
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The Baylis-Hillman reaction using methyl crotonate and 2-cyclohexen-1-one as electron-deficient alkenes scarcely proceeds in the presence of 3-HQD under high pressure induced by water-freezing. As acrylonitrile, a reactive electron-deficient alkene, reacts with aldehydes under normal pressure to afford the Baylis-Hillman adducts in good yield, it is not necessary to use high pressure induced by water-freezing.
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The Baylis-Hillman reaction using methyl crotonate and 2-cyclohexen-1-one as electron-deficient alkenes scarcely proceeds in the presence of 3-HQD under high pressure induced by water-freezing. As acrylonitrile, a reactive electron-deficient alkene, reacts with aldehydes under normal pressure to afford the Baylis-Hillman adducts in good yield, it is not necessary to use high pressure induced by water-freezing.
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