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Volumn 6, Issue 19, 2004, Pages 3241-3244

Intramolecular [3 + 2]-cycloaddition reaction of push-pull dipoles across heteroaromatic π-systems

Author keywords

[No Author keywords available]

Indexed keywords

IMIDE; RUTHENIUM COMPLEX;

EID: 4644302114     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol048915w     Document Type: Article
Times cited : (61)

References (35)
  • 2
    • 0000541874 scopus 로고
    • The Therapeutic Use of Bisindole Alkaloids from Catharanthus
    • Brossi, A., Suffness, M., Eds.; Academic Press: New York
    • Neus, N.; Neus, M. N. The Therapeutic Use of Bisindole Alkaloids from Catharanthus. In The Alkaloids; Brossi, A., Suffness, M., Eds.; Academic Press: New York, 1990; Vol. 37, p 232.
    • (1990) The Alkaloids , vol.37 , pp. 232
    • Neus, N.1    Neus, M.N.2
  • 3
    • 85013528497 scopus 로고
    • Bisindole Alkaloids
    • Rodrigo, R. G. A., Ed.; Academic Press, Inc.: San Diego
    • Cordell, G. A.; Saxton, J. E. Bisindole Alkaloids. In The Alkaloids; Rodrigo, R. G. A., Ed.; Academic Press, Inc.: San Diego, 1981; Vol. 20.
    • (1981) The Alkaloids , vol.20
    • Cordell, G.A.1    Saxton, J.E.2
  • 4
    • 0002837763 scopus 로고
    • Isolation, Structure Elucidation and Biosynthesis of the Bisindole Catharanthus
    • Brossi, A., Suffness, M., Eds.; Academic Press: New York
    • Blasko, G.; Cordell, G. A. Isolation, Structure Elucidation and Biosynthesis of the Bisindole Catharanthus. In The Alkaloids; Brossi, A., Suffness, M., Eds.; Academic Press: New York, 1990; Vol. 37, p 12.
    • (1990) The Alkaloids , vol.37 , pp. 12
    • Blasko, G.1    Cordell, G.A.2
  • 5
    • 0002837763 scopus 로고
    • Antitumor Bisindole Alkaloids from Catharanthus roseus (L.)
    • Academic Press: New York, Chapter 2
    • For a review on synthetic studies of vinblastine, see: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). In The Alkaloids; Brossi, A., Suffness. M., Eds.; Academic Press: New York, 1990; Vol. 37, Chapter 2, pp 77-131.
    • (1990) The Alkaloids , vol.37 , pp. 77-131
    • Brossi, A.1    Suffness, M.2
  • 15
  • 20
    • 4644354206 scopus 로고    scopus 로고
    • note
    • 2Ph, CN, etc.) as well as an eventual intramolecular nucleophilic N-C bond formation.
  • 28
    • 0000426796 scopus 로고    scopus 로고
    • Harmata, M., Ed.; JAI Press
    • Indole is quite a good dienophile in inverse electron demand Diels-Alder cycloadditions; see: Lee, L.; Snyder, J. K. Advances in Cycloaddition Chemistry; Harmata, M., Ed.; JAI Press: 1999; Vol. 6, p 119.
    • (1999) Advances in Cycloaddition Chemistry , vol.6 , pp. 119
    • Lee, L.1    Snyder, J.K.2
  • 32
    • 33845374099 scopus 로고
    • (b) Carruthers, W. Cycloaddition Reactions in Organic Synthesis; Pergamon Press: Oxford, 1990. Lipshutz, B. H. Chem. Rev. 1986, 86, 795.
    • (1986) Chem. Rev. , vol.86 , pp. 795
    • Lipshutz, B.H.1
  • 35
    • 4644275597 scopus 로고    scopus 로고
    • note
    • Conversion of 21 to 22 was previously described in ref 13.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.