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Volumn 6, Issue 12, 2004, Pages 2075-2078

New asymmetric halo aldol reaction provides a novel approach to biologically important chiral cyclothers and cycloamines

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALDEHYDE; AMINE; BASE; CARBONYL DERIVATIVE; ETHER DERIVATIVE; TETRAHYDROFURAN DERIVATIVE;

EID: 3042790177     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol049255y     Document Type: Article
Times cited : (19)

References (38)
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    • For representative references on asymmetric catalytic aldol reactions, see: (a) Bach, T. Angew. Chem., Int. Ed. Engl. 1994, 33, 417-419. (b) Enders, D.; Ince, S. J. Synthesis 2002, 619-624. (c) Corey, E. J.; Cywin, C. L.; Roper, T. D. Tetrahedron Lett. 1992, 33, 6907-6910. (d) Evans, D. A.; Kozlowski, M. C.; Murray, J. A.; Burgey, C. S.; Campos, B. T.; Staples, R. J. J. Am. Chem. Soc. 1999, 121, 669-685. (e) Groger, H.; Vogl, E. M.; Shibasaki, M. Chem. Eur. J. 1998, 4, 1137-1141.
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    • For representative references on asymmetric catalytic aldol reactions, see: (a) Bach, T. Angew. Chem., Int. Ed. Engl. 1994, 33, 417-419. (b) Enders, D.; Ince, S. J. Synthesis 2002, 619-624. (c) Corey, E. J.; Cywin, C. L.; Roper, T. D. Tetrahedron Lett. 1992, 33, 6907-6910. (d) Evans, D. A.; Kozlowski, M. C.; Murray, J. A.; Burgey, C. S.; Campos, B. T.; Staples, R. J. J. Am. Chem. Soc. 1999, 121, 669-685. (e) Groger, H.; Vogl, E. M.; Shibasaki, M. Chem. Eur. J. 1998, 4, 1137-1141.
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    • For representative references on asymmetric catalytic aldol reactions, see: (a) Bach, T. Angew. Chem., Int. Ed. Engl. 1994, 33, 417-419. (b) Enders, D.; Ince, S. J. Synthesis 2002, 619-624. (c) Corey, E. J.; Cywin, C. L.; Roper, T. D. Tetrahedron Lett. 1992, 33, 6907-6910. (d) Evans, D. A.; Kozlowski, M. C.; Murray, J. A.; Burgey, C. S.; Campos, B. T.; Staples, R. J. J. Am. Chem. Soc. 1999, 121, 669-685. (e) Groger, H.; Vogl, E. M.; Shibasaki, M. Chem. Eur. J. 1998, 4, 1137-1141.
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    • For representative references on asymmetric catalytic aldol reactions, see: (a) Bach, T. Angew. Chem., Int. Ed. Engl. 1994, 33, 417-419. (b) Enders, D.; Ince, S. J. Synthesis 2002, 619-624. (c) Corey, E. J.; Cywin, C. L.; Roper, T. D. Tetrahedron Lett. 1992, 33, 6907-6910. (d) Evans, D. A.; Kozlowski, M. C.; Murray, J. A.; Burgey, C. S.; Campos, B. T.; Staples, R. J. J. Am. Chem. Soc. 1999, 121, 669-685. (e) Groger, H.; Vogl, E. M.; Shibasaki, M. Chem. Eur. J. 1998, 4, 1137-1141.
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    • For recent racemic halo aldol reaction, see: (a) Kataoka, T.; Kinoshita, H.; Kinoshita, S.; Iwamura, T.; Watanable, S. Angew. Chem., Int. Ed. 2000, 39, 2358-2360. (b) Wei, H.-X.; Caputo, T. D.; Purkiss, D. W.; Li, G. Tetrahedron 2000, 56, 2397-2401. (c) Uehira, S.; Han, Z.; Shinokubo, H.; Oshima, K. J. Org. Chem. 2001, 66, 7854-7857. (d) Li, G.; Wei, H.-X.; Caputo, T. D. Tetrahedron Lett. 2000, 41, 1-4. (e) Shi, M.; Jiang, J.-K.; Feng, Y.-S. Org. Lett. 2000, 2, 2397-2400.
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    • Kataoka, T.1    Kinoshita, H.2    Kinoshita, S.3    Iwamura, T.4    Watanable, S.5
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    • For recent racemic halo aldol reaction, see: (a) Kataoka, T.; Kinoshita, H.; Kinoshita, S.; Iwamura, T.; Watanable, S. Angew. Chem., Int. Ed. 2000, 39, 2358-2360. (b) Wei, H.-X.; Caputo, T. D.; Purkiss, D. W.; Li, G. Tetrahedron 2000, 56, 2397-2401. (c) Uehira, S.; Han, Z.; Shinokubo, H.; Oshima, K. J. Org. Chem. 2001, 66, 7854-7857. (d) Li, G.; Wei, H.-X.; Caputo, T. D. Tetrahedron Lett. 2000, 41, 1-4. (e) Shi, M.; Jiang, J.-K.; Feng, Y.-S. Org. Lett. 2000, 2, 2397-2400.
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    • Wei, H.-X.1    Caputo, T.D.2    Purkiss, D.W.3    Li, G.4
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    • For recent racemic halo aldol reaction, see: (a) Kataoka, T.; Kinoshita, H.; Kinoshita, S.; Iwamura, T.; Watanable, S. Angew. Chem., Int. Ed. 2000, 39, 2358-2360. (b) Wei, H.-X.; Caputo, T. D.; Purkiss, D. W.; Li, G. Tetrahedron 2000, 56, 2397-2401. (c) Uehira, S.; Han, Z.; Shinokubo, H.; Oshima, K. J. Org. Chem. 2001, 66, 7854-7857. (d) Li, G.; Wei, H.-X.; Caputo, T. D. Tetrahedron Lett. 2000, 41, 1-4. (e) Shi, M.; Jiang, J.-K.; Feng, Y.-S. Org. Lett. 2000, 2, 2397-2400.
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    • Uehira, S.1    Han, Z.2    Shinokubo, H.3    Oshima, K.4
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    • For recent racemic halo aldol reaction, see: (a) Kataoka, T.; Kinoshita, H.; Kinoshita, S.; Iwamura, T.; Watanable, S. Angew. Chem., Int. Ed. 2000, 39, 2358-2360. (b) Wei, H.-X.; Caputo, T. D.; Purkiss, D. W.; Li, G. Tetrahedron 2000, 56, 2397-2401. (c) Uehira, S.; Han, Z.; Shinokubo, H.; Oshima, K. J. Org. Chem. 2001, 66, 7854-7857. (d) Li, G.; Wei, H.-X.; Caputo, T. D. Tetrahedron Lett. 2000, 41, 1-4. (e) Shi, M.; Jiang, J.-K.; Feng, Y.-S. Org. Lett. 2000, 2, 2397-2400.
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    • Li, G.1    Wei, H.-X.2    Caputo, T.D.3
  • 18
    • 0000884769 scopus 로고    scopus 로고
    • For recent racemic halo aldol reaction, see: (a) Kataoka, T.; Kinoshita, H.; Kinoshita, S.; Iwamura, T.; Watanable, S. Angew. Chem., Int. Ed. 2000, 39, 2358-2360. (b) Wei, H.-X.; Caputo, T. D.; Purkiss, D. W.; Li, G. Tetrahedron 2000, 56, 2397-2401. (c) Uehira, S.; Han, Z.; Shinokubo, H.; Oshima, K. J. Org. Chem. 2001, 66, 7854-7857. (d) Li, G.; Wei, H.-X.; Caputo, T. D. Tetrahedron Lett. 2000, 41, 1-4. (e) Shi, M.; Jiang, J.-K.; Feng, Y.-S. Org. Lett. 2000, 2, 2397-2400.
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    • Shi, M.1    Jiang, J.-K.2    Feng, Y.-S.3
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    • For a racemic aldol reaction of cyclopropyl ketone, see: (a) Han, Z.; Uehira, S.; Tsuritani, T.; Shinokubo, H.; Oshima, K. Tetrahedron 2001, 57, 987-995. (b) Takami, K.; Mikami, S.; Yorimitsu, H.; Shinokubo, H.; Oshima, K. Tetrahedron 2003, 59, 6627-6635.
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    • Han, Z.1    Uehira, S.2    Tsuritani, T.3    Shinokubo, H.4    Oshima, K.5
  • 26
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    • For a racemic aldol reaction of cyclopropyl ketone, see: (a) Han, Z.; Uehira, S.; Tsuritani, T.; Shinokubo, H.; Oshima, K. Tetrahedron 2001, 57, 987-995. (b) Takami, K.; Mikami, S.; Yorimitsu, H.; Shinokubo, H.; Oshima, K. Tetrahedron 2003, 59, 6627-6635.
    • (2003) Tetrahedron , vol.59 , pp. 6627-6635
    • Takami, K.1    Mikami, S.2    Yorimitsu, H.3    Shinokubo, H.4    Oshima, K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.