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Volumn , Issue 2, 2004, Pages 406-412

Synthesis and Biological Activity of Point-Fluorinated Pheromone Analogues of Eldana saccharina

Author keywords

Asymmetric synthesis; Bioorganic chemistry; Fluorine; Pheromones; Radical reaction

Indexed keywords

FLUORINE; PHEROMONE DERIVATIVE;

EID: 0842284210     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200300541     Document Type: Article
Times cited : (31)

References (32)
  • 3
  • 23
    • 0842299456 scopus 로고    scopus 로고
    • (Eds.: W. J. Lough, I. W. Eainer), Blackwell Science, CRC Press, UK, and references cited therein
    • [13b] K. Mori, in Chirality in Natural and Applied Science (Eds.: W. J. Lough, I. W. Eainer), Blackwell Science, CRC Press, UK, 2002, pp. 241-259 and references cited therein.
    • (2002) Chirality in Natural, Applied Science , pp. 241-259
    • Mori, K.1
  • 24
    • 0842320892 scopus 로고    scopus 로고
    • note
    • MasSpartan Pro was employed for the semi-empirical calculation.
  • 25
    • 0001846892 scopus 로고    scopus 로고
    • A. Sekiguchi, T. Matsuo, R. Akaba, Bull. Chem. Soc. Jpn. 1998, 71, 41-47. The geometry of the trimethylenecyclopentene derivative determined by X-ray diffraction was successfully reproduced by a PM3 calculation. A semi-empirical calculation (AMI level) was also used successfully for predicting the effect that fluorine substitution has on the thermodynamics: S. F. Nelson, S. J. Klein, D. A. Trieber II, R. F. Ismagilov, D. R. Powell, J. Org. Chem. 1997, 62, 6539-6546.
    • (1998) Bull. Chem. Soc. Jpn. , vol.71 , pp. 41-47
    • Sekiguchi, A.1    Matsuo, T.2    Akaba, R.3
  • 26
    • 0000180939 scopus 로고    scopus 로고
    • A. Sekiguchi, T. Matsuo, R. Akaba, Bull. Chem. Soc. Jpn. 1998, 71, 41-47. The geometry of the trimethylenecyclopentene derivative determined by X-ray diffraction was successfully reproduced by a PM3 calculation. A semi-empirical calculation (AMI level) was also used successfully for predicting the effect that fluorine substitution has on the thermodynamics: S. F. Nelson, S. J. Klein, D. A. Trieber II, R. F. Ismagilov, D. R. Powell, J. Org. Chem. 1997, 62, 6539-6546.
    • (1997) J. Org. Chem. , vol.62 , pp. 6539-6546
    • Nelson, S.F.1    Klein, S.J.2    Trieber II, D.A.3    Ismagilov, R.F.4    Powell, D.R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.