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Volumn 33, Issue 5, 1996, Pages 1437-1443

Development of methodology for amide oxidation and its application to total synthesis of Securinega alkaloids

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; ANISOMYCIN; ANTIBIOTIC AGENT; SECURININE;

EID: 0029827222     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570330503     Document Type: Article
Times cited : (7)

References (34)
  • 1
    • 37049173494 scopus 로고
    • D. H. Hey and D. G. Turpin, J. Chem. Soc., 2471 (1954); D. H. Hey, C. W. Rees and A. R. Todd, J. Chem. Soc. (C), 1518 (1967).
    • (1954) J. Chem. Soc. , pp. 2471
    • Hey, D.H.1    Turpin, D.G.2
  • 4
    • 2942545129 scopus 로고
    • For a review of radical reactions of arenediazonium ions, see: C. Galli, Chem. Rev., 88, 765 (1988).
    • (1988) Chem. Rev. , vol.88 , pp. 765
    • Galli, C.1
  • 5
    • 0001427539 scopus 로고
    • E. Steckhan, ed., Springer-Verlag: Berlin
    • For a review, see: T. Shono in Topics in Current Chemistry; E. Steckhan, ed., Springer-Verlag: Berlin, 1988, Vol. 148, p. 131. See also P. Magnus, C. Hulme and W. Welser, J. Am. Chem. Soc., 116, 4501 (1994) for a chemical method for amide oxidation.
    • (1988) Topics in Current Chemistry , vol.148 , pp. 131
    • Shono, T.1
  • 6
    • 0005945259 scopus 로고
    • For a review, see: T. Shono in Topics in Current Chemistry; E. Steckhan, ed., Springer-Verlag: Berlin, 1988, Vol. 148, p. 131. See also P. Magnus, C. Hulme and W. Welser, J. Am. Chem. Soc., 116, 4501 (1994) for a chemical method for amide oxidation.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 4501
    • Magnus, P.1    Hulme, C.2    Welser, W.3
  • 8
    • 0003062656 scopus 로고
    • M. C. Venuti, Synthesis, 266 (1982). For a review of isatoic anhydride chemistry, see: G. M. Coppola, Synthesis, 505 (1980).
    • (1982) Synthesis , pp. 266
    • Venuti, M.C.1
  • 9
    • 85069762576 scopus 로고
    • M. C. Venuti, Synthesis, 266 (1982). For a review of isatoic anhydride chemistry, see: G. M. Coppola, Synthesis, 505 (1980).
    • (1980) Synthesis , pp. 505
    • Coppola, G.M.1
  • 20
    • 10544241366 scopus 로고    scopus 로고
    • 1H NMR, but one does not know which of the possible intermediates between the aniline and the aryl radical undergoes equilibration of rotamers [11,12]
    • 1H NMR, but one does not know which of the possible intermediates between the aniline and the aryl radical undergoes equilibration of rotamers [11,12].
  • 22
    • 0023549451 scopus 로고
    • For reviews, see J. A. Beutler and A. N. Brubaker, Drugs of the Future, 12, 957 (1987); V. Snieckus, The Securinega Alkaloids in The Alkaloids, R. H. F. Manske, ed., 1975, Vol. 14, p. 425.
    • (1987) Drugs of the Future , vol.12 , pp. 957
    • Beutler, J.A.1    Brubaker, A.N.2
  • 23
    • 0012364324 scopus 로고
    • The Securinega Alkaloids
    • R. H. F. Manske, ed.
    • For reviews, see J. A. Beutler and A. N. Brubaker, Drugs of the Future, 12, 957 (1987); V. Snieckus, The Securinega Alkaloids in The Alkaloids, R. H. F. Manske, ed., 1975, Vol. 14, p. 425.
    • (1975) The Alkaloids , vol.14 , pp. 425
    • Snieckus, V.1
  • 27
    • 0008790449 scopus 로고
    • C. H. Heathcock, R. A. Jennings and T. W. von Geldern, J. Org. Chem., 48, 3428 (1983); C. H. Heathcock and T. W. von Geldern, Heterocycles, 25, 75 (1987).
    • (1987) Heterocycles , vol.25 , pp. 75
    • Heathcock, C.H.1    Von Geldern, T.W.2
  • 33
    • 33845277902 scopus 로고
    • For lead references, see: T. K. Hayes, R. Villani and S. M. Weinreb, J. Am. Chem. Soc., 110, 5533 (1988); J. H. Udding, K. J. M. Tuijp, M. N. A. van Zanden, H. Hiemstra and W. N. Speckamp, J. Org. Chem., 59, 1993 (1994).
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 5533
    • Hayes, T.K.1    Villani, R.2    Weinreb, S.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.