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Volumn 33, Issue 43, 1992, Pages 6511-6514

Iodoetherification of homoallylic alcohols : A stereoselective approach to tetrahydrofurans

Author keywords

[No Author keywords available]

Indexed keywords

TETRAHYDROFURAN DERIVATIVE;

EID: 0026662563     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)79029-0     Document Type: Article
Times cited : (49)

References (26)
  • 2
    • 0001881753 scopus 로고
    • Cyclization Forming Carbon-Heteroatom Bonds
    • J.D. Morrison, Academic Press, Orlanda
    • (1984) Asymmetric Syntheses , vol.3 , pp. 144
    • Bartlett1
  • 6
    • 85083020006 scopus 로고
    • Halocyclization of Unsaturated Alcohols and Carboxylic Acids Using Bis(sym-collidine)iodine(I) Perchlorate
    • [mCPBA, 18-crown-6, NaI, CH2Cl2], [bis(sym-collidine)IClO4]
    • (1988) Synthesis , pp. 862
    • Evans1    Magee2    Schauble3
  • 14
    • 33751553184 scopus 로고
    • Stereo- and regiocontrol of electrophilic additions to cyclohexene systems by neighboring groups. Competition of electronic and stereoelectronic effects and comparison of the reactivity of selected electrophiles
    • [aryltellurinyl acetate], [steroidal examples]
    • (1990) The Journal of Organic Chemistry , vol.55 , pp. 5580
    • Kocovsky1    Pour2
  • 15
    • 0000257461 scopus 로고
    • Episulphonium ion-induced cyclisations generally give poor results with homoallylic alcohols, see for example
    • (1987) Tetrahedron Lett. , vol.28 , pp. 523
    • Tuladhar1    Fallis2
  • 18
    • 84919176192 scopus 로고    scopus 로고
    • S. B. Bedford, K. E. Bell, G. Fenton, D. W. Knight and D. Shaw, preceding paper.
  • 23
    • 84919176191 scopus 로고    scopus 로고
    • 4 reduction. The (Z)-isomer 11 was obtained by Lindlar reduction of the initial alkynol.
  • 25
    • 84919176190 scopus 로고    scopus 로고
    • Satisfactory spectroscopic and analytical data have been obtained for this compound.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.