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Volumn , Issue 20, 1999, Pages 2061-2062

Two-step synthesis of homochiral monoaminals of tricarbonylphthalaldehydechromium complex

Author keywords

[No Author keywords available]

Indexed keywords

ALKENYL GROUP; BENZENE DERIVATIVE; CARBONYL DERIVATIVE; CHROMIUM DERIVATIVE; DIAMINE; METAL COMPLEX; MONOAMINE DERIVATIVE; PHTHALALDEHYDE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

EID: 0033592546     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/a906043j     Document Type: Article
Times cited : (7)

References (23)
  • 1
    • 0009740870 scopus 로고    scopus 로고
    • F. Rose-Munch and E. Rose, Curr. Org. Chem., 1999, 3, 493; F. Rose-Munch, V. Gagliardini, C. Renard and E. Rose, Coord. Chem. Rev., 1998, 178-180, 249; M. F. Semmelhack, in Comprehensive Organometallic Chemistry II, ed. E. W. Abel, F. G. A. Stone and G. Wilkinson, Pergamon, Oxford, 1995, vol. 12, p. 979.
    • (1999) Curr. Org. Chem. , vol.3 , pp. 493
    • Rose-Munch, F.1    Rose, E.2
  • 2
    • 0032263206 scopus 로고    scopus 로고
    • F. Rose-Munch and E. Rose, Curr. Org. Chem., 1999, 3, 493; F. Rose-Munch, V. Gagliardini, C. Renard and E. Rose, Coord. Chem. Rev., 1998, 178-180, 249; M. F. Semmelhack, in Comprehensive Organometallic Chemistry II, ed. E. W. Abel, F. G. A. Stone and G. Wilkinson, Pergamon, Oxford, 1995, vol. 12, p. 979.
    • (1998) Coord. Chem. Rev. , vol.178-180 , pp. 249
    • Rose-Munch, F.1    Gagliardini, V.2    Renard, C.3    Rose, E.4
  • 3
    • 0000747080 scopus 로고
    • ed. E. W. Abel, F. G. A. Stone and G. Wilkinson, Pergamon, Oxford
    • F. Rose-Munch and E. Rose, Curr. Org. Chem., 1999, 3, 493; F. Rose-Munch, V. Gagliardini, C. Renard and E. Rose, Coord. Chem. Rev., 1998, 178-180, 249; M. F. Semmelhack, in Comprehensive Organometallic Chemistry II, ed. E. W. Abel, F. G. A. Stone and G. Wilkinson, Pergamon, Oxford, 1995, vol. 12, p. 979.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 979
    • Semmelhack, M.F.1
  • 4
    • 0032980511 scopus 로고    scopus 로고
    • See for example: B. Schnell, G. Bernardinelli and E. P. Kündig, Synlett, 1999, 3, 348; E. P. Kündig, D. Armurrio, G. Anderson, D. Beruhen, K. Khan, A. Ripa and L. Ronggang, Pure Appl. Chem., 1997, 69, 543; A. Solladié-Cavallo, G. Solladié and E. Tsamo, J. Org. Chem., 1979, 44, 4189; G. Jaouen and A. Meyer, J. Am. Chem. Soc., 1975, 97, 4667.
    • (1999) Synlett , vol.3 , pp. 348
    • Schnell, B.1    Bernardinelli, G.2    Kündig, E.P.3
  • 5
    • 0038401539 scopus 로고    scopus 로고
    • See for example: B. Schnell, G. Bernardinelli and E. P. Kündig, Synlett, 1999, 3, 348; E. P. Kündig, D. Armurrio, G. Anderson, D. Beruhen, K. Khan, A. Ripa and L. Ronggang, Pure Appl. Chem., 1997, 69, 543; A. Solladié-Cavallo, G. Solladié and E. Tsamo, J. Org. Chem., 1979, 44, 4189; G. Jaouen and A. Meyer, J. Am. Chem. Soc., 1975, 97, 4667.
    • (1997) Pure Appl. Chem. , vol.69 , pp. 543
    • Kündig, E.P.1    Armurrio, D.2    Anderson, G.3    Beruhen, D.4    Khan, K.5    Ripa, A.6    Ronggang, L.7
  • 6
    • 33845561075 scopus 로고
    • See for example: B. Schnell, G. Bernardinelli and E. P. Kündig, Synlett, 1999, 3, 348; E. P. Kündig, D. Armurrio, G. Anderson, D. Beruhen, K. Khan, A. Ripa and L. Ronggang, Pure Appl. Chem., 1997, 69, 543; A. Solladié-Cavallo, G. Solladié and E. Tsamo, J. Org. Chem., 1979, 44, 4189; G. Jaouen and A. Meyer, J. Am. Chem. Soc., 1975, 97, 4667.
    • (1979) J. Org. Chem. , vol.44 , pp. 4189
    • Solladié-Cavallo, A.1    Solladié, G.2    Tsamo, E.3
  • 7
    • 0001636874 scopus 로고
    • See for example: B. Schnell, G. Bernardinelli and E. P. Kündig, Synlett, 1999, 3, 348; E. P. Kündig, D. Armurrio, G. Anderson, D. Beruhen, K. Khan, A. Ripa and L. Ronggang, Pure Appl. Chem., 1997, 69, 543; A. Solladié-Cavallo, G. Solladié and E. Tsamo, J. Org. Chem., 1979, 44, 4189; G. Jaouen and A. Meyer, J. Am. Chem. Soc., 1975, 97, 4667.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 4667
    • Jaouen, G.1    Meyer, A.2
  • 13
    • 0344338012 scopus 로고
    • S. Top, G. Jaouen, J. Gillois, C. Baldoli and S. Maiorana, J. Chem. Soc., Chem. Commun., 1988, 284; B. Malézieux, G. Jaouen, J. Salatin, J. A. S. Howell, M. G. Palin, P. McArdle and M. O'Gara, Tetrahedron: Asymmetry, 1995, 3, 375; K. Nakamura, K. Ishihara, A. Ohno, A. Uemura, H. Nishimura and Y. Hayashi, Tetrahedron Lett., 1990, 31, 3603.
    • (1988) J. Chem. Soc., Chem. Commun. , pp. 284
    • Top, S.1    Jaouen, G.2    Gillois, J.3    Baldoli, C.4    Maiorana, S.5
  • 15
    • 0025332802 scopus 로고
    • S. Top, G. Jaouen, J. Gillois, C. Baldoli and S. Maiorana, J. Chem. Soc., Chem. Commun., 1988, 284; B. Malézieux, G. Jaouen, J. Salatin, J. A. S. Howell, M. G. Palin, P. McArdle and M. O'Gara, Tetrahedron: Asymmetry, 1995, 3, 375; K. Nakamura, K. Ishihara, A. Ohno, A. Uemura, H. Nishimura and Y. Hayashi, Tetrahedron Lett., 1990, 31, 3603.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 3603
    • Nakamura, K.1    Ishihara, K.2    Ohno, A.3    Uemura, A.4    Nishimura, H.5    Hayashi, Y.6
  • 19
    • 0345632497 scopus 로고    scopus 로고
    • D. Thesis, Paris
    • (a) A. Perrotey, D. Thesis, Paris, 1996;
    • (1996)
    • Perrotey, A.1
  • 20
    • 0345632496 scopus 로고    scopus 로고
    • The same sequence (1→→3) was applied by E. P. Kündig and H. Ratni in 65% yield with a different hydrolysing system: private communication
    • (b) The same sequence (1→→3) was applied by E. P. Kündig and H. Ratni in 65% yield with a different hydrolysing system: private communication.
  • 22
    • 0001267078 scopus 로고
    • D. L. Commins and J. D. Brown, J. Org. Chem., 1984, 49, 1078; the asymmetric version was developed earlier: see ref. 7(b) and R. A. Ewin, A. M. Macleod, D.A. Price, N.S. Simpkins and A.P.Watt, J. Chem. Soc., Perkin Trans. 1, 1997, 401.
    • (1984) J. Org. Chem. , vol.49 , pp. 1078
    • Commins, D.L.1    Brown, J.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.