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Volumn , Issue 9, 1984, Pages 578-579

Total synthesis of (+)- and (−)-frontalin

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Indexed keywords


EID: 37049113744     PISSN: 00224936     EISSN: None     Source Type: Journal    
DOI: 10.1039/C39840000578     Document Type: Article
Times cited : (16)

References (11)
  • 2
    • 0019785840 scopus 로고
    • references therein
    • R. M. Silverstein, Science, 1981, 213, 1326, and references therein.
    • (1981) Science , vol.213 , pp. 1326
    • Silverstein, R.M.1
  • 3
    • 0002773537 scopus 로고
    • ed. J. ApSimon, Wiley, New York, ch. 1
    • A detailed account of the synthesis of optically active insect pheromones appeared recently: K. Mori in ‘The Total Synthesis of Natural Products,’ ed. J. ApSimon, Wiley, New York, 1981, vol. 4, ch. 1
    • (1981) The Total Synthesis of Natural Products , vol.4
    • Mori, K.1
  • 8
    • 0010640653 scopus 로고
    • The enantiomeric excess was determined by the methoxy(trifluoromethyl)phenylacetyl ester method
    • J. A. Dale, D. L. Dull, and G. S. Mosher, J. Org. Chem., 1969, 34, 2543.
    • (1969) J. Org. Chem , vol.34 , pp. 2543
    • Mosher, G.S.1
  • 10
    • 0020645466 scopus 로고
    • Some of our recent efforts in the synthesis of optically pure natural products have been reported
    • Some of our recent efforts in the synthesis of optically pure natural products have been reported: S. Y. Ko, A. W. M. Lee, S. Masamune, L. A. Reed III, K. B. Sharpless, and F. J. Walker, Science, 1983, 220, 949
    • (1983) Science , vol.220 , pp. 949
    • Ko, S.Y.1    Lee, A.W.M.2    Masamune, S.3    Reed, L.A.4    Sharpless, K.B.5    Walker, F.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.