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Volumn 6, Issue 17, 2004, Pages 2953-2956

New synthetic method for indole-2-carboxylate and its application to the total synthesis of duocarmycin SA

Author keywords

[No Author keywords available]

Indexed keywords

2 INDOLECARBOXYLIC ACID; CARBOXYLIC ACID DERIVATIVE; DUOCARMYCIN SA; HALIDE; PALLADIUM;

EID: 4444243019     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0489548     Document Type: Article
Times cited : (64)

References (26)
  • 2
    • 0001426611 scopus 로고    scopus 로고
    • Katritzky, A. R., Ress, C. W., Scriven, E. F. V., Bird, C. W., Eds.; Pergamon Press: Oxford
    • (b) Sundberg, R. J. Comprehensive Heterocyclic Chemistry II; Katritzky, A. R., Ress, C. W., Scriven, E. F. V., Bird, C. W., Eds.; Pergamon Press: Oxford, 1996; Vol. 2, p 119.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.2 , pp. 119
    • Sundberg, R.J.1
  • 9
    • 4444293021 scopus 로고    scopus 로고
    • note
    • The reason for the low conversion of the electron rich compounds is not totally clear, but one possibility may be the presence of an undesired deactivation cycle of the catalyst.
  • 10
    • 0141852845 scopus 로고    scopus 로고
    • For examples, see: (a) Esseveldt, B, C, J.; Delft, F. L.; Gelder, R.; Rutjes, F. P. J. T. Org. Lett. 2003, 5, 1717. (b) Larock, R. C.; Yum, E. K.; Refvik, M. D. J. Org. Chem. 1998, 63, 7652. (c) Yu, M. S.; Leon, L. L.; McGguire, M. A.; Botha, G. Tetrahedron Lett. 1998, 39, 9347.
    • (2003) Org. Lett. , vol.5 , pp. 1717
    • Esseveldt, B.C.J.1    Delft, F.L.2    Gelder, R.3    Rutjes, F.P.J.T.4
  • 11
    • 33744870975 scopus 로고    scopus 로고
    • For examples, see: (a) Esseveldt, B, C, J.; Delft, F. L.; Gelder, R.; Rutjes, F. P. J. T. Org. Lett. 2003, 5, 1717. (b) Larock, R. C.; Yum, E. K.; Refvik, M. D. J. Org. Chem. 1998, 63, 7652. (c) Yu, M. S.; Leon, L. L.; McGguire, M. A.; Botha, G. Tetrahedron Lett. 1998, 39, 9347.
    • (1998) J. Org. Chem. , vol.63 , pp. 7652
    • Larock, R.C.1    Yum, E.K.2    Refvik, M.D.3
  • 12
    • 0032542178 scopus 로고    scopus 로고
    • For examples, see: (a) Esseveldt, B, C, J.; Delft, F. L.; Gelder, R.; Rutjes, F. P. J. T. Org. Lett. 2003, 5, 1717. (b) Larock, R. C.; Yum, E. K.; Refvik, M. D. J. Org. Chem. 1998, 63, 7652. (c) Yu, M. S.; Leon, L. L.; McGguire, M. A.; Botha, G. Tetrahedron Lett. 1998, 39, 9347.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 9347
    • Yu, M.S.1    Leon, L.L.2    McGguire, M.A.3    Botha, G.4
  • 24
    • 4444273828 scopus 로고    scopus 로고
    • note
    • More than half of the epoxide 23 was decomposed during the isolation and the purification. Therefore, 23 could not be characterized.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.