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Volumn 59, Issue 44, 2003, Pages 8833-8841

Synthesis and reactivity of Z and E functionalized allylic fluorides

Author keywords

Allylic fluoride; Enal; Enone; Fluorine

Indexed keywords

4 FLUORO 1 PHENYLNON 2 EN 1 ONE; ALLYL COMPOUND; FLUORINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0141892778     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2003.08.068     Document Type: Article
Times cited : (7)

References (19)
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    • Chemistry of organic fluorine compounds II: A critical review
    • ACS, Washington, DC
    • See, for instance: (a) Hudlicky M., Pavlath A.E. Chemistry of Organic Fluorine Compounds II: A Critical Review. ACS Monograph 187. 1995;ACS, Washington, DC, (b) Kitazume T., Yamazaki T. Experimental Methods in Organic Fluorine Chemistry. 1998;Gordon & Breach, Tokyo. and references therein.
    • (1995) ACS Monograph , vol.187
  • 2
    • 0003698431 scopus 로고    scopus 로고
    • Gordon & Breach, Tokyo. and references therein
    • See, for instance: (a) Hudlicky M., Pavlath A.E. Chemistry of Organic Fluorine Compounds II: A Critical Review. ACS Monograph 187. 1995;ACS, Washington, DC, (b) Kitazume T., Yamazaki T. Experimental Methods in Organic Fluorine Chemistry. 1998;Gordon & Breach, Tokyo. and references therein.
    • (1998) Experimental Methods in Organic Fluorine Chemistry
    • Kitazume, T.1    Yamazaki, T.2
  • 3
    • 0023237559 scopus 로고    scopus 로고
    • See, for instance: (a) Welch J.T. Tetrahedron. 43:1987;3123-3193 (b) Resnati G. Tetrahedron. 49:1993;9385-9445 (c) Welch J.T., Eswarakrishnan S. Fluorine in Bioorganic Chemistry. 1991;Wiley Interscience, New York, (d) Ojima I., McCarthy J.R., Welch J.T. Biomedical Frontiers in Fluorine Chemistry. ACS Symposium Series 639. 1996;ACS, Washington, DC. and references therein.
    • (1987) Tetrahedron , vol.43 , pp. 3123-3193
    • Welch, J.T.1
  • 4
    • 0027432004 scopus 로고
    • See, for instance: (a) Welch J.T. Tetrahedron. 43:1987;3123-3193 (b) Resnati G. Tetrahedron. 49:1993;9385-9445 (c) Welch J.T., Eswarakrishnan S. Fluorine in Bioorganic Chemistry. 1991;Wiley Interscience, New York, (d) Ojima I., McCarthy J.R., Welch J.T. Biomedical Frontiers in Fluorine Chemistry. ACS Symposium Series 639. 1996;ACS, Washington, DC. and references therein.
    • (1993) Tetrahedron , vol.49 , pp. 9385-9445
    • Resnati, G.1
  • 5
    • 0023237559 scopus 로고    scopus 로고
    • Wiley Interscience, New York
    • See, for instance: (a) Welch J.T. Tetrahedron. 43:1987;3123-3193 (b) Resnati G. Tetrahedron. 49:1993;9385-9445 (c) Welch J.T., Eswarakrishnan S. Fluorine in Bioorganic Chemistry. 1991;Wiley Interscience, New York, (d) Ojima I., McCarthy J.R., Welch J.T. Biomedical Frontiers in Fluorine Chemistry. ACS Symposium Series 639. 1996;ACS, Washington, DC. and references therein.
    • (1991) Fluorine in Bioorganic Chemistry
    • Welch, J.T.1    Eswarakrishnan, S.2
  • 6
    • 0023237559 scopus 로고    scopus 로고
    • Biomedical frontiers in fluorine chemistry
    • ACS, Washington, DC. and references therein
    • See, for instance: (a) Welch J.T. Tetrahedron. 43:1987;3123-3193 (b) Resnati G. Tetrahedron. 49:1993;9385-9445 (c) Welch J.T., Eswarakrishnan S. Fluorine in Bioorganic Chemistry. 1991;Wiley Interscience, New York, (d) Ojima I., McCarthy J.R., Welch J.T. Biomedical Frontiers in Fluorine Chemistry. ACS Symposium Series 639. 1996;ACS, Washington, DC. and references therein.
    • (1996) ACS Symposium Series , vol.639
    • Ojima, I.1    McCarthy, J.R.2    Welch, J.T.3
  • 8
    • 33847800447 scopus 로고
    • (a) For a classical example see: Middleton W.J. J. Org. Chem. 40:1975;574-578. (b) For a recent example see: De Jonghe S., Van Overmeire I., Poulton S., Hendrix C., Busson R., Van Calenbergh S., De Keukeleire D., Spiegel S., Herdewijn P. Bioorg. Med. Chem. Lett. 9:1999;3175-3180.
    • (1975) J. Org. Chem. , vol.40 , pp. 574-578
    • Middleton, W.J.1
  • 18
    • 85031061809 scopus 로고    scopus 로고
    • If heating is maintained for longer periods the decomposition of 1a starts, possibly by autocatalytic processes, affording unidentified compounds
    • If heating is maintained for longer periods the decomposition of 1a starts, possibly by autocatalytic processes, affording unidentified compounds.
  • 19
    • 85031061912 scopus 로고    scopus 로고
    • 2 at room temperature to perform this Z to E isomerisation
    • 2 at room temperature to perform this Z to E isomerisation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.