메뉴 건너뛰기




Volumn , Issue 9, 1999, Pages 1477-1479

Efficient generation of trifluoroacetaldehyde and successive reaction with imines affording β-hydroxy-β-trifluoromethyl ketones

Author keywords

Hemiacetal; Hydrate; Imine; Trifluoroacetaldehyde; hydroxy trifluoromethyl ketones

Indexed keywords

ALDEHYDE DERIVATIVE; FLUORINE DERIVATIVE; KETONE DERIVATIVE;

EID: 0032844214     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-2870     Document Type: Article
Times cited : (22)

References (35)
  • 1
    • 0029908069 scopus 로고    scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1996) Chem. Pharm. Bull. , vol.44 , pp. 2003
    • Iseki, K.1    Oishi, S.2    Kobayashi, Y.3
  • 2
    • 0029656223 scopus 로고    scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1996) Tetrahedron , vol.52 , pp. 71
    • Iseki, K.1    Oishi, S.2    Kobayashi, Y.3
  • 3
    • 0029147247 scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 6527
    • Makino, Y.1    Iseki, K.2    Fujii, K.3    Oishi, S.4    Hirano, T.5    Kobayashi, Y.6
  • 4
    • 0011886420 scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1994) Chem. Lett. , pp. 1135
    • Iseki, K.1    Oishi, S.2    Kobayashi, Y.3
  • 5
    • 0023686354 scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 4665
    • Patel, D.V.1    Rielly-Gauvin, K.2    Ryono, D.E.3
  • 6
    • 0029656027 scopus 로고    scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1996) Tetrahedron , vol.52 , pp. 85
    • Mikami, K.1    Yajima, T.2    Takasaki, T.3    Matsukawa, S.4    Terada, M.5    Uchimaru, T.6    Maruta, M.7
  • 7
    • 2742513913 scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1995) Synlett , pp. 1057
    • Mikami, K.1    Takasaki, T.2    Matsukawa, S.3    Maruta, M.4
  • 8
    • 0342738672 scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1985) J. Fluorine Chem. , vol.30 , pp. 357
    • Yamazaki, T.1    Takita, K.2    Ishikawa, N.3
  • 9
    • 0344164437 scopus 로고    scopus 로고
    • Yokohama, May, Abstr. No. P50.
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1999) The International Conference on Fluorine Chemistry '99 Tokyo
    • Ishii, A.1    Mikami, K.2
  • 10
    • 0242558656 scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1968) Bull. Soc. Chim. Fr. , pp. 1182
    • Pautrat, R.1    Marteau, J.2    Cheritat, R.3
  • 11
    • 0025874577 scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1991) Chem. Pharm. Bull. , vol.39 , pp. 1707
    • Ogawa, K.1    Nagai, T.2    Nonomura, M.3    Takagi, T.4    Koyama, M.5    Ando, A.6    Miki, T.7    Kumadaki, I.8
  • 12
    • 0002393793 scopus 로고    scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1996) Synlett , pp. 837
    • Mikami, K.1    Yajima, T.2    Siree, N.3    Terada, M.4    Suzuki, Y.5    Kobayashi, I.6
  • 13
    • 0028289510 scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1994) Tetrahedron: Asymmetry , vol.5 , pp. 1087
    • Mikami, K.1    Yajima, T.2    Terada, M.3    Kato, E.4    Maruta, M.5
  • 14
    • 0027449158 scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 7591
    • Mikami, K.1    Yajima, T.2    Terada, M.3    Uchimaru, T.4
  • 15
    • 0343852969 scopus 로고    scopus 로고
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 6001
    • Lévêque, L.1    Blanc, M.L.2    Pastor, R.3
  • 16
    • 0242558654 scopus 로고    scopus 로고
    • Tokyo, March, Abstr. No. 4H332
    • For the reaction with boron enolates, see: Iseki, K.; Oishi, S.; Kobayashi, Y. Chem. Pharm. Bull. 1996, 44, 2003. Iseki, K.; Oishi S.; Kobayashi, Y. Tetrahedron 1996, 52, 71. Makino, Y.; Iseki, K.; Fujii, K.; Oishi, S.; Hirano T.; Kobayashi, Y. Tetrahedron Lett. 1995, 36, 6527. Iseki, K.; Oishi S.; Kobayashi, Y. Chem. Lett. 1994, 1135. For with a lithium enolate, see: Patel, D. V.; Rielly-Gauvin, K.; Ryono, D. E. Tetrahedron Lett. 1988, 29, 4665. For with ketene silyl acetal, see: Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Tetrahedron 1996, 52, 85. Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Synlett 1995, 1057. For with a lithium reagent, see: Yamazaki, T.; Takita K.; Ishikawa, N. J. Fluorine Chem. 1985, 30, 357. For asymmetric Friedel-Crafts reaction, see: Ishii, A.; Mikami, K. The International Conference on Fluorine Chemistry '99 Tokyo, Yokohama, May, 1999, Abstr. No. P50. For ene reaction, see: Pautrat, R.; Marteau J.; Cheritat, R. Bull. Soc. Chim. Fr. 1968, 1182. Ogawa, K.; Nagai, T.; Nonomura, M.; Takagi, T.; Koyama, M.; Ando, A.; Miki, T.; Kumadaki, I. Chem. Pharm. Bull. 1991, 39, 1707. For asymmetric ene reaction, see: Mikami, K.; Yajima, T.; Siree, N.; Terada, M.; Suzuki, Y.; Kobayashi, I. Synlett 1996, 837. Mikami, K.; Yajima, T.; Terada, M.; Kato, E.; Maruta, M. Tetrahedron: Asymmetry 1994, 5, 1087. Mikami, K.; Yajima, T.; Terada, M.; Uchimaru, T. Tetrahedron Lett. 1993, 34, 7591. For Hetero Diels-Alder reaction, see: Lévêque, L.; Blanc, M. L.; Pastor, R. Tetrahedron Lett. 1997, 38, 6001. For asymmetric Hetero Diels-Alder reaction, see: Mikami, K.; Takasaki, T.; Yajima, T.; Matsukawa, S.; Terada, M. 72nd National Meeting of the Chemical Society of Japan, Tokyo, March, 1997, Abstr. No. 4H332.
    • (1997) 72nd National Meeting of the Chemical Society of Japan
    • Mikami, K.1    Takasaki, T.2    Yajima, T.3    Matsukawa, S.4    Terada, M.5
  • 17
    • 0006152221 scopus 로고    scopus 로고
    • For recent examples dealing with the preparation and the reaction of trifluoroacetaldehyde equivalents, see: Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Chem. Commun. 1998, 1259. Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Synlett, 1998, 1353. Poras, H.; Matsutani, H.; Yaruva, J.; Kusumoto, T.; Hiyama, T. Chem. Lett. 1998, 665. Xu, Y.; Dolbier, Jr., W. R. Tetrahedron Lett. 1998, 39, 9151. Folléas, B.; Marek, I.; Normant, J. F.; Jalmes, L. S. Tetrahedron Lett. 1998, 39, 2973. Russell, J.; Roques, N. Tetrahedron 1998, 54, 13771. Wiedemann, J.; Heiner, T.; Mloston, G.; Prakash, G. K. S.; Olah, G. A. Angew. Chem., Int. Ed. Engl. 1998, 37, 820. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Tetrahedron Lett. 1998, 39, 1199. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Chem. Lett. 1998, 119. Ishii, A.; Higashiyama, K.; Mikami, K. Synlett 1997, 1381. Loh, T. -P.; Li, X. -R. Chem. Commun. 1996, 1929.
    • (1998) Chem. Commun. , pp. 1259
    • Matsutani, H.1    Poras, H.2    Kusumoto, T.3    Hiyama, T.4
  • 18
    • 0002656727 scopus 로고    scopus 로고
    • For recent examples dealing with the preparation and the reaction of trifluoroacetaldehyde equivalents, see: Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Chem. Commun. 1998, 1259. Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Synlett, 1998, 1353. Poras, H.; Matsutani, H.; Yaruva, J.; Kusumoto, T.; Hiyama, T. Chem. Lett. 1998, 665. Xu, Y.; Dolbier, Jr., W. R. Tetrahedron Lett. 1998, 39, 9151. Folléas, B.; Marek, I.; Normant, J. F.; Jalmes, L. S. Tetrahedron Lett. 1998, 39, 2973. Russell, J.; Roques, N. Tetrahedron 1998, 54, 13771. Wiedemann, J.; Heiner, T.; Mloston, G.; Prakash, G. K. S.; Olah, G. A. Angew. Chem., Int. Ed. Engl. 1998, 37, 820. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Tetrahedron Lett. 1998, 39, 1199. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Chem. Lett. 1998, 119. Ishii, A.; Higashiyama, K.; Mikami, K. Synlett 1997, 1381. Loh, T. -P.; Li, X. -R. Chem. Commun. 1996, 1929.
    • (1998) Synlett , pp. 1353
    • Matsutani, H.1    Poras, H.2    Kusumoto, T.3    Hiyama, T.4
  • 19
    • 0032363793 scopus 로고    scopus 로고
    • For recent examples dealing with the preparation and the reaction of trifluoroacetaldehyde equivalents, see: Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Chem. Commun. 1998, 1259. Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Synlett, 1998, 1353. Poras, H.; Matsutani, H.; Yaruva, J.; Kusumoto, T.; Hiyama, T. Chem. Lett. 1998, 665. Xu, Y.; Dolbier, Jr., W. R. Tetrahedron Lett. 1998, 39, 9151. Folléas, B.; Marek, I.; Normant, J. F.; Jalmes, L. S. Tetrahedron Lett. 1998, 39, 2973. Russell, J.; Roques, N. Tetrahedron 1998, 54, 13771. Wiedemann, J.; Heiner, T.; Mloston, G.; Prakash, G. K. S.; Olah, G. A. Angew. Chem., Int. Ed. Engl. 1998, 37, 820. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Tetrahedron Lett. 1998, 39, 1199. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Chem. Lett. 1998, 119. Ishii, A.; Higashiyama, K.; Mikami, K. Synlett 1997, 1381. Loh, T. -P.; Li, X. -R. Chem. Commun. 1996, 1929.
    • (1998) Chem. Lett. , pp. 665
    • Poras, H.1    Matsutani, H.2    Yaruva, J.3    Kusumoto, T.4    Hiyama, T.5
  • 20
    • 0032506573 scopus 로고    scopus 로고
    • For recent examples dealing with the preparation and the reaction of trifluoroacetaldehyde equivalents, see: Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Chem. Commun. 1998, 1259. Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Synlett, 1998, 1353. Poras, H.; Matsutani, H.; Yaruva, J.; Kusumoto, T.; Hiyama, T. Chem. Lett. 1998, 665. Xu, Y.; Dolbier, Jr., W. R. Tetrahedron Lett. 1998, 39, 9151. Folléas, B.; Marek, I.; Normant, J. F.; Jalmes, L. S. Tetrahedron Lett. 1998, 39, 2973. Russell, J.; Roques, N. Tetrahedron 1998, 54, 13771. Wiedemann, J.; Heiner, T.; Mloston, G.; Prakash, G. K. S.; Olah, G. A. Angew. Chem., Int. Ed. Engl. 1998, 37, 820. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Tetrahedron Lett. 1998, 39, 1199. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Chem. Lett. 1998, 119. Ishii, A.; Higashiyama, K.; Mikami, K. Synlett 1997, 1381. Loh, T. -P.; Li, X. -R. Chem. Commun. 1996, 1929.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 9151
    • Xu, Y.1    Dolbier W.R., Jr.2
  • 21
    • 0032492981 scopus 로고    scopus 로고
    • For recent examples dealing with the preparation and the reaction of trifluoroacetaldehyde equivalents, see: Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Chem. Commun. 1998, 1259. Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Synlett, 1998, 1353. Poras, H.; Matsutani, H.; Yaruva, J.; Kusumoto, T.; Hiyama, T. Chem. Lett. 1998, 665. Xu, Y.; Dolbier, Jr., W. R. Tetrahedron Lett. 1998, 39, 9151. Folléas, B.; Marek, I.; Normant, J. F.; Jalmes, L. S. Tetrahedron Lett. 1998, 39, 2973. Russell, J.; Roques, N. Tetrahedron 1998, 54, 13771. Wiedemann, J.; Heiner, T.; Mloston, G.; Prakash, G. K. S.; Olah, G. A. Angew. Chem., Int. Ed. Engl. 1998, 37, 820. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Tetrahedron Lett. 1998, 39, 1199. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Chem. Lett. 1998, 119. Ishii, A.; Higashiyama, K.; Mikami, K. Synlett 1997, 1381. Loh, T. -P.; Li, X. -R. Chem. Commun. 1996, 1929.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2973
    • Folléas, B.1    Marek, I.2    Normant, J.F.3    Jalmes, L.S.4
  • 22
    • 0032487852 scopus 로고    scopus 로고
    • For recent examples dealing with the preparation and the reaction of trifluoroacetaldehyde equivalents, see: Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Chem. Commun. 1998, 1259. Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Synlett, 1998, 1353. Poras, H.; Matsutani, H.; Yaruva, J.; Kusumoto, T.; Hiyama, T. Chem. Lett. 1998, 665. Xu, Y.; Dolbier, Jr., W. R. Tetrahedron Lett. 1998, 39, 9151. Folléas, B.; Marek, I.; Normant, J. F.; Jalmes, L. S. Tetrahedron Lett. 1998, 39, 2973. Russell, J.; Roques, N. Tetrahedron 1998, 54, 13771. Wiedemann, J.; Heiner, T.; Mloston, G.; Prakash, G. K. S.; Olah, G. A. Angew. Chem., Int. Ed. Engl. 1998, 37, 820. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Tetrahedron Lett. 1998, 39, 1199. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Chem. Lett. 1998, 119. Ishii, A.; Higashiyama, K.; Mikami, K. Synlett 1997, 1381. Loh, T. -P.; Li, X. -R. Chem. Commun. 1996, 1929.
    • (1998) Tetrahedron , vol.54 , pp. 13771
    • Russell, J.1    Roques, N.2
  • 23
    • 0031949090 scopus 로고    scopus 로고
    • For recent examples dealing with the preparation and the reaction of trifluoroacetaldehyde equivalents, see: Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Chem. Commun. 1998, 1259. Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Synlett, 1998, 1353. Poras, H.; Matsutani, H.; Yaruva, J.; Kusumoto, T.; Hiyama, T. Chem. Lett. 1998, 665. Xu, Y.; Dolbier, Jr., W. R. Tetrahedron Lett. 1998, 39, 9151. Folléas, B.; Marek, I.; Normant, J. F.; Jalmes, L. S. Tetrahedron Lett. 1998, 39, 2973. Russell, J.; Roques, N. Tetrahedron 1998, 54, 13771. Wiedemann, J.; Heiner, T.; Mloston, G.; Prakash, G. K. S.; Olah, G. A. Angew. Chem., Int. Ed. Engl. 1998, 37, 820. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Tetrahedron Lett. 1998, 39, 1199. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Chem. Lett. 1998, 119. Ishii, A.; Higashiyama, K.; Mikami, K. Synlett 1997, 1381. Loh, T. -P.; Li, X. -R. Chem. Commun. 1996, 1929.
    • (1998) Angew. Chem., Int. Ed. Engl. , vol.37 , pp. 820
    • Wiedemann, J.1    Heiner, T.2    Mloston, G.3    Prakash, G.K.S.4    Olah, G.A.5
  • 24
    • 0032485520 scopus 로고    scopus 로고
    • For recent examples dealing with the preparation and the reaction of trifluoroacetaldehyde equivalents, see: Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Chem. Commun. 1998, 1259. Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Synlett, 1998, 1353. Poras, H.; Matsutani, H.; Yaruva, J.; Kusumoto, T.; Hiyama, T. Chem. Lett. 1998, 665. Xu, Y.; Dolbier, Jr., W. R. Tetrahedron Lett. 1998, 39, 9151. Folléas, B.; Marek, I.; Normant, J. F.; Jalmes, L. S. Tetrahedron Lett. 1998, 39, 2973. Russell, J.; Roques, N. Tetrahedron 1998, 54, 13771. Wiedemann, J.; Heiner, T.; Mloston, G.; Prakash, G. K. S.; Olah, G. A. Angew. Chem., Int. Ed. Engl. 1998, 37, 820. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Tetrahedron Lett. 1998, 39, 1199. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Chem. Lett. 1998, 119. Ishii, A.; Higashiyama, K.; Mikami, K. Synlett 1997, 1381. Loh, T. -P.; Li, X. -R. Chem. Commun. 1996, 1929.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 1199
    • Ishii, A.1    Miyamoto, F.2    Higashiyama, K.3    Mikami, K.4
  • 25
    • 0032387023 scopus 로고    scopus 로고
    • For recent examples dealing with the preparation and the reaction of trifluoroacetaldehyde equivalents, see: Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Chem. Commun. 1998, 1259. Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Synlett, 1998, 1353. Poras, H.; Matsutani, H.; Yaruva, J.; Kusumoto, T.; Hiyama, T. Chem. Lett. 1998, 665. Xu, Y.; Dolbier, Jr., W. R. Tetrahedron Lett. 1998, 39, 9151. Folléas, B.; Marek, I.; Normant, J. F.; Jalmes, L. S. Tetrahedron Lett. 1998, 39, 2973. Russell, J.; Roques, N. Tetrahedron 1998, 54, 13771. Wiedemann, J.; Heiner, T.; Mloston, G.; Prakash, G. K. S.; Olah, G. A. Angew. Chem., Int. Ed. Engl. 1998, 37, 820. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Tetrahedron Lett. 1998, 39, 1199. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Chem. Lett. 1998, 119. Ishii, A.; Higashiyama, K.; Mikami, K. Synlett 1997, 1381. Loh, T. -P.; Li, X. -R. Chem. Commun. 1996, 1929.
    • (1998) Chem. Lett. , pp. 119
    • Ishii, A.1    Miyamoto, F.2    Higashiyama, K.3    Mikami, K.4
  • 26
    • 0000646412 scopus 로고    scopus 로고
    • For recent examples dealing with the preparation and the reaction of trifluoroacetaldehyde equivalents, see: Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Chem. Commun. 1998, 1259. Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Synlett, 1998, 1353. Poras, H.; Matsutani, H.; Yaruva, J.; Kusumoto, T.; Hiyama, T. Chem. Lett. 1998, 665. Xu, Y.; Dolbier, Jr., W. R. Tetrahedron Lett. 1998, 39, 9151. Folléas, B.; Marek, I.; Normant, J. F.; Jalmes, L. S. Tetrahedron Lett. 1998, 39, 2973. Russell, J.; Roques, N. Tetrahedron 1998, 54, 13771. Wiedemann, J.; Heiner, T.; Mloston, G.; Prakash, G. K. S.; Olah, G. A. Angew. Chem., Int. Ed. Engl. 1998, 37, 820. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Tetrahedron Lett. 1998, 39, 1199. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Chem. Lett. 1998, 119. Ishii, A.; Higashiyama, K.; Mikami, K. Synlett 1997, 1381. Loh, T. -P.; Li, X. -R. Chem. Commun. 1996, 1929.
    • (1997) Synlett , pp. 1381
    • Ishii, A.1    Higashiyama, K.2    Mikami, K.3
  • 27
    • 0002600063 scopus 로고    scopus 로고
    • For recent examples dealing with the preparation and the reaction of trifluoroacetaldehyde equivalents, see: Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Chem. Commun. 1998, 1259. Matsutani, H.; Poras, H.; Kusumoto, T.; Hiyama, T. Synlett, 1998, 1353. Poras, H.; Matsutani, H.; Yaruva, J.; Kusumoto, T.; Hiyama, T. Chem. Lett. 1998, 665. Xu, Y.; Dolbier, Jr., W. R. Tetrahedron Lett. 1998, 39, 9151. Folléas, B.; Marek, I.; Normant, J. F.; Jalmes, L. S. Tetrahedron Lett. 1998, 39, 2973. Russell, J.; Roques, N. Tetrahedron 1998, 54, 13771. Wiedemann, J.; Heiner, T.; Mloston, G.; Prakash, G. K. S.; Olah, G. A. Angew. Chem., Int. Ed. Engl. 1998, 37, 820. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Tetrahedron Lett. 1998, 39, 1199. Ishii, A.; Miyamoto, F.; Higashiyama, K.; Mikami, K. Chem. Lett. 1998, 119. Ishii, A.; Higashiyama, K.; Mikami, K. Synlett 1997, 1381. Loh, T. -P.; Li, X. -R. Chem. Commun. 1996, 1929.
    • (1996) Chem. Commun. , pp. 1929
    • Loh, T.-P.1    Li, X.-R.2
  • 28
    • 0001562073 scopus 로고
    • Braid, M.; Isersone, H.; Lawlore, F. E. J. Am. Chem. Soc. 1954, 76, 4027. Henne, A. L.; Pelley, R. L.; Alm, R. M. J. Am. Chem. Soc. 1950, 72, 3370. Shechter, H.; Conrad, F. J. Am. Chem. Soc. 1950, 72, 3371.
    • (1954) J. Am. Chem. Soc. , vol.76 , pp. 4027
    • Braid, M.1    Isersone, H.2    Lawlore, F.E.3
  • 29
    • 0242391596 scopus 로고
    • Braid, M.; Isersone, H.; Lawlore, F. E. J. Am. Chem. Soc. 1954, 76, 4027. Henne, A. L.; Pelley, R. L.; Alm, R. M. J. Am. Chem. Soc. 1950, 72, 3370. Shechter, H.; Conrad, F. J. Am. Chem. Soc. 1950, 72, 3371.
    • (1950) J. Am. Chem. Soc. , vol.72 , pp. 3370
    • Henne, A.L.1    Pelley, R.L.2    Alm, R.M.3
  • 30
    • 0000696404 scopus 로고
    • Braid, M.; Isersone, H.; Lawlore, F. E. J. Am. Chem. Soc. 1954, 76, 4027. Henne, A. L.; Pelley, R. L.; Alm, R. M. J. Am. Chem. Soc. 1950, 72, 3370. Shechter, H.; Conrad, F. J. Am. Chem. Soc. 1950, 72, 3371.
    • (1950) J. Am. Chem. Soc. , vol.72 , pp. 3371
    • Shechter, H.1    Conrad, F.2
  • 32
    • 0344596002 scopus 로고    scopus 로고
    • note
    • 2: M, 218.0555.
  • 33
    • 33748600216 scopus 로고
    • Arend, M.; Risch, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 2639. Pfau, M.; Revial, G.; Guingant, A.; d'Angelo, J. J. Am. Chem. Soc. 1985, 107, 273, and references cited therein.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 2639
    • Arend, M.1    Risch, N.2
  • 34
    • 0000257169 scopus 로고
    • and references cited therein
    • Arend, M.; Risch, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 2639. Pfau, M.; Revial, G.; Guingant, A.; d'Angelo, J. J. Am. Chem. Soc. 1985, 107, 273, and references cited therein.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 273
    • Pfau, M.1    Revial, G.2    Guingant, A.3    D'Angelo, J.4
  • 35
    • 0345026992 scopus 로고    scopus 로고
    • Trifluoroacetaldehyde hydrate (75 wt%), which contains 25 wt% water, was used
    • Trifluoroacetaldehyde hydrate (75 wt%), which contains 25 wt% water, was used.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.