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Volumn 17, Issue 8, 1984, Pages 289-296

Nucleophilic Additions to Tetrahydropyridinium Salts. Applications to Alkaloid Syntheses

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EID: 0001542017     PISSN: 00014842     EISSN: 15204898     Source Type: Journal    
DOI: 10.1021/ar00104a005     Document Type: Article
Times cited : (210)

References (61)
  • 1
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    • (2) Webster defines heuristic as “serving to discover or to stimulate investigation; of methods of demonstration which tend to lead a person to investigate further”
    • Stevens, R. V. Acc. Chem. Res. 1977, 10, 193. (2) Webster defines heuristic as “serving to discover or to stimulate investigation; of methods of demonstration which tend to lead a person to investigate further”.
    • (1977) Acc. Chem. Res. , vol.10 , pp. 193
    • Stevens, R.V.1
  • 2
    • 0041729067 scopus 로고
    • For a stimulating earlier overview see
    • For a stimulating earlier overview see: Ayer, W. A.; Browne, L. M. Heterocycles 1977, 7, 685.
    • (1977) Heterocycles , vol.7 , pp. 685
    • Ayer, W.A.1    Browne, L.M.2
  • 3
    • 0017067762 scopus 로고
    • For previous syntheses of these compounds see
    • For previous syntheses of these compounds see: Ayer, W. A.; Furuichi, K. Can. J. Chem. 1976, 54, 1494.
    • (1976) Can. J. Chem. , vol.54 , pp. 1494
    • Ayer, W.A.1    Furuichi, K.2
  • 8
    • 0040648440 scopus 로고
    • For an interesting discussion of the reaction and synthesis, see John Wiley and Sons: London
    • For an interesting discussion of the reaction and synthesis, see: Fleming, I. “Selected Organic Syntheses”; John Wiley and Sons: London, 1973; p 17.
    • (1973) Selected Organic Syntheses , pp. 17
    • Fleming, I.1
  • 10
    • 85022884721 scopus 로고
    • For a valuable discussion of many aspects of stereoelectronic control see Baldwin, J. E., Ed.; Pergamon Press: Oxford and references cited therein
    • For a valuable discussion of many aspects of stereoelectronic control see: Deslongchamps, P. In “Organic Chemistry Series”; Baldwin, J. E., Ed.; Pergamon Press: Oxford, 1983; Vol. 1, p 211 and references cited therein.
    • (1983) Organic Chemistry Series , vol.1 , pp. 211
    • Deslongchamps, P.1
  • 28
    • 85022809786 scopus 로고    scopus 로고
    • unpublished results, University of California, Los Angeles
    • Stevens, R. V.; Nakagawa, Y., unpublished results, University of California, Los Angeles.
    • Stevens, R.V.1    Nakagawa, Y.2
  • 32
    • 0009644246 scopus 로고
    • Isolation of makomakine
    • Isolation of makomakine: Bick, I. R. C.; Hai, M. A. Heterocycles 1981, 16, 1301.
    • (1981) Heterocycles , vol.16 , pp. 1301
    • Bick, I.R.C.1    Hai, M.A.2
  • 35
    • 0008327501 scopus 로고
    • For another synthesis of makomakine see
    • For another synthesis of makomakine see: Mirand, C.; Massiot, G.; Levy, J. J. Org. Chem. 1982, 47, 4169.
    • (1982) J. Org. Chem. , vol.47 , pp. 4169
    • Mirand, C.1    Massiot, G.2    Levy, J.3
  • 37
    • 0005806603 scopus 로고
    • For other examples of additions to the more sterically hindered face see
    • For other examples of additions to the more sterically hindered face see: Riediker, M.; Graf, W. Helv. Chim. Acta 1979, 62, 2053.
    • (1979) Helv. Chim. Acta , vol.62 , pp. 2053
    • Riediker, M.1    Graf, W.2
  • 48
    • 0004215714 scopus 로고
    • Marcel Dekker, Inc.: New York
    • Cook, A. G. “Enamines”; Marcel Dekker, Inc.: New York, 1969; pp 1-51.
    • (1969) Enamines , pp. 1-51
    • Cook, A.G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.