메뉴 건너뛰기




Volumn 37, Issue 44, 1996, Pages 8053-8056

Enantioselective synthesis of fusarentin methyl ethers: Insecticidal metabolites of Fusarium larvarum

Author keywords

[No Author keywords available]

Indexed keywords

FUSARENTIN DERIVATIVE; INSECTICIDE; UNCLASSIFIED DRUG;

EID: 0030605169     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01823-0     Document Type: Article
Times cited : (26)

References (24)
  • 9
    • 0002232692 scopus 로고
    • The synthesis of 3-substituted isocoumarins by acylation of 6-methoxytoluate esters with N-methoxy-N-methyl-carboxamides followed by cyclisation of the resulting ketoesters has been reported
    • 9. The synthesis of 3-substituted isocoumarins by acylation of 6-methoxytoluate esters with N-methoxy-N-methyl-carboxamides followed by cyclisation of the resulting ketoesters has been reported: Lewis, C. N.; Spargo, P. L.; Staunton, J., Synthesis, 1986, 944.
    • (1986) Synthesis , pp. 944
    • Lewis, C.N.1    Spargo, P.L.2    Staunton, J.3
  • 10
    • 0021234656 scopus 로고
    • Condensation of o-toluamide anions with aromatic aldehydes followed by base hydrolysis gives 3-aryl-3,4-dihydroisocoumarins in modest yield
    • 10. Condensation of o-toluamide anions with aromatic aldehydes followed by base hydrolysis gives 3-aryl-3,4-dihydroisocoumarins in modest yield: Watanabe, M.; Sahara, M.; Kubo, M.; Furukawa, S.; Billedeau, R. J.; Snieckus, V., J. Org. Chem., 1984, 49, 742.
    • (1984) J. Org. Chem. , vol.49 , pp. 742
    • Watanabe, M.1    Sahara, M.2    Kubo, M.3    Furukawa, S.4    Billedeau, R.J.5    Snieckus, V.6
  • 11
    • 85030284500 scopus 로고    scopus 로고
    • note
    • 11. All new compounds gave satisfactory spectroscopic and analytical data which will be reported in full elsewhere.
  • 12
    • 85030289609 scopus 로고    scopus 로고
    • note
    • 2]bromoacetic acid.
  • 16
    • 0000376088 scopus 로고
    • The e.e. was determined after ethanolysis of (12) and conversion to the (S)-(-)-MTPA ester
    • 16. The e.e. was determined after ethanolysis of (12) and conversion to the (S)-(-)-MTPA ester: Carreira, E. M.; Singer, R. A.; Lee, W., J. Am. Chem. Soc., 1994, 116, 8837.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 8837
    • Carreira, E.M.1    Singer, R.A.2    Lee, W.3
  • 19
    • 84970567192 scopus 로고
    • 18. Sargent, M. V.; Vogel, P.; Elix, A., J. Chem. Soc., Perkin Trans. 1, 1975, 1986; Elix, J. A.; Jayanthi, V. K., Aust. J. Chem., 1981, 34, 1153.
    • (1981) Aust. J. Chem. , vol.34 , pp. 1153
    • Elix, J.A.1    Jayanthi, V.K.2
  • 24
    • 0000985525 scopus 로고    scopus 로고
    • The acid catalysed hydrolysis proceeds considerably faster than base catalysed hydrolysis reported in similar systems
    • 23. The acid catalysed hydrolysis proceeds considerably faster than base catalysed hydrolysis reported in similar systems : Salvadori, P.; Superchi, S.; Minutolo, F., J. Org. Chem., 1996, 61, 4190.
    • (1996) J. Org. Chem. , vol.61 , pp. 4190
    • Salvadori, P.1    Superchi, S.2    Minutolo, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.