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Volumn 52, Issue 19, 1996, Pages 6647-6664

Rearrangement of α-Hydroxy Imines to α-Amino Ketones : Mechanistic Aspects and Synthetic Applications

Author keywords

[No Author keywords available]

Indexed keywords

AMINOKETONE; PERHYDROHISTRIONICOTOXIN;

EID: 0029932015     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00317-1     Document Type: Article
Times cited : (33)

References (48)
  • 2
    • 0016593869 scopus 로고
    • eds. Herz, W. ; Grisebach, H. and Kirby, G.W. Springer Verlag, New York
    • Sammes, P.G. in Fortschifte der Chemie Organisher Naturstoffe, eds. Herz, W. ; Grisebach, H. and Kirby, G.W. Springer Verlag, New York 1975, 32, pp 51-117.
    • (1975) Fortschifte der Chemie Organisher Naturstoffe , vol.32 , pp. 51-117
    • Sammes, P.G.1
  • 3
    • 0007247327 scopus 로고
    • For examples of total synthesis of Aristotelia alkaloids see : (a) Borschberg, H.J. Chimia 1991, 45, 329-341
    • (1991) Chimia , vol.45 , pp. 329-341
    • Borschberg, H.J.1
  • 5
    • 0001150248 scopus 로고
    • For total synthesis of natural products containing 2,5-dioxopiperazine moiety see for example : (a) Hutchinson, A.J. ; Kishi, Y. J.Am.Chem.Soc. 1979, 101, 6786-6788;
    • (1979) J.Am.Chem.Soc. , vol.101 , pp. 6786-6788
    • Hutchinson, A.J.1    Kishi, Y.2
  • 17
    • 85030016480 scopus 로고    scopus 로고
    • 13
    • 13.
  • 23
    • 85030010016 scopus 로고    scopus 로고
    • Enantiomeric excess of compounds 12d,h,i was determined either by NMR-LIS experiments (12d) or by comparison of the sign of their specific rotation with that of an authentic sample of known optical purity (12h,i)
    • Enantiomeric excess of compounds 12d,h,i was determined either by NMR-LIS experiments (12d) or by comparison of the sign of their specific rotation with that of an authentic sample of known optical purity (12h,i).
  • 29
    • 0000902959 scopus 로고
    • Daub, G.W. ; Heerding, D.A. ; Overman, L.A. Tetrahedron 1988, 44, 3919-3930. Castro, P. ; Overman, L.E. ; Zhang, X. ; Mariano, P.S.Tetrahedron Lett. 1993, 34, 5243-5246.
    • (1988) Tetrahedron , vol.44 , pp. 3919-3930
    • Daub, G.W.1    Heerding, D.A.2    Overman, L.A.3
  • 33
    • 37049096299 scopus 로고
    • Pearson, A.J. ; Ham, P. J.Chem.Soc. Perkin Trans.I, 1983, 1421-1425 ; Godleski, S.A. ; Heacok, D.J. ; Meinhart, J.D. ; Wallendael, S.V. J.Org.Chem. 1983, 48, 2101-2103.
    • (1983) J.Chem.Soc. Perkin Trans.I , pp. 1421-1425
    • Pearson, A.J.1    Ham, P.2
  • 40
    • 0020336489 scopus 로고
    • Herz,W. ; Grisebach, H. ; Kirby, G.W. eds ; Springer-Verlag, Berlin
    • Daly, J.W. in Progress in the Organic Chemistry of Natural Products ; Herz,W. ; Grisebach, H. ; Kirby, G.W. eds ; Springer-Verlag, Berlin 1982, pp 205-340 ; Witkop, B. ; Gossinger, E. in the Alkaloids ; Brossi, A. ed. ; Academic Press, New-York 1983, pp 139-251.
    • (1982) Progress in the Organic Chemistry of Natural Products , pp. 205-340
    • Daly, J.W.1
  • 41
    • 77957097677 scopus 로고
    • Brossi, A. ed. ; Academic Press, New-York
    • Daly, J.W. in Progress in the Organic Chemistry of Natural Products ; Herz,W. ; Grisebach, H. ; Kirby, G.W. eds ; Springer-Verlag, Berlin 1982, pp 205-340 ; Witkop, B. ; Gossinger, E. in the Alkaloids ; Brossi, A. ed. ; Academic Press, New-York 1983, pp 139-251.
    • (1983) The Alkaloids , pp. 139-251
    • Witkop, B.1    Gossinger, E.2
  • 45
    • 85030025006 scopus 로고    scopus 로고
    • 4 (12.5 ml, 98%) and AcOH (2 ml, glacial) slowly to a stirred solution of anisaldehyde (12.5 ml) in EtOH (215 ml)
    • 4 (12.5 ml, 98%) and AcOH (2 ml, glacial) slowly to a stirred solution of anisaldehyde (12.5 ml) in EtOH (215 ml).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.