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Volumn 43, Issue 37, 2002, Pages 6637-6640

Construction of functionalised medium rings by stereospecific expansions of 2,3-epoxy alcohols under mild conditions

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; EPOXIDE; KETONE; TIN CHLORIDE;

EID: 0037048505     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01450-8     Document Type: Article
Times cited : (16)

References (24)
  • 3
    • 0000688199 scopus 로고
    • B.M. Trost, & I. Fleming. New York: Pergamon Press
    • Hanson J.R. Trost B.M., Fleming I., Comprehensive Organic Synthesis. 3:1991;705-719 Pergamon Press, New York.
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 705-719
    • Hanson, J.R.1
  • 8
    • 0001726756 scopus 로고
    • B.M. Trost, & I. Fleming. New York: Pergamon Press
    • Coveney D.J. Trost B.M., Fleming I., Comprehensive Organic Synthesis. 3:1991;777-799 Pergamon Press, New York.
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 777-799
    • Coveney, D.J.1
  • 10
    • 0011209107 scopus 로고    scopus 로고
    • note
    • 4) and evaporated under reduced pressure. The residue was purified by column chromatography to give the β-hydroxyketone 6d as a colourless oil.
  • 12
    • 0000457807 scopus 로고
    • . 1-Lithio-1-phenylpropenes were prepared from the corresponding 1-chloro-1-phenylpropenes by reaction with lithium in diethyl ether: Larson S.D., Grieco P.A., Fobare W.F. J. Am. Chem. Soc. 108:1986;3512.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 3512
    • Larson, S.D.1    Grieco, P.A.2    Fobare, W.F.3
  • 13
    • 0011247435 scopus 로고    scopus 로고
    • Reaction of 2-bromobut-2-enes with magnesium turnings in THF at gentle reflux afforded the Grignard reagents used to prepare the allylic alcohol precursors required for 5c, 5f, 5g and 5h
    • Reaction of 2-bromobut-2-enes with magnesium turnings in THF at gentle reflux afforded the Grignard reagents used to prepare the allylic alcohol precursors required for 5c, 5f, 5g and 5h.
  • 14
    • 0011196222 scopus 로고    scopus 로고
    • Relative configurations of the allylic alcohols and the corresponding epoxy alcohols were confirmed by NOE experiments
    • Relative configurations of the allylic alcohols and the corresponding epoxy alcohols were confirmed by NOE experiments.
  • 23
    • 0003417469 scopus 로고
    • B.M. Trost, & I. Fleming. New York: Pergamon Press
    • Heathcock C.H. Trost B.M., Fleming I., Comprehensive Organic Synthesis. 2:1991;147-150 Pergamon Press, New York.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 147-150
    • Heathcock, C.H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.