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0003132806
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Chemistry of organic fluorine compounds II: A critical review
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ACS, Washington, DC
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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.
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(1995)
ACS Monograph
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Gordon & Breach, Tokyo. and references therein
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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.
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Experimental Methods in Organic Fluorine Chemistry
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Kitazume, T.1
Yamazaki, T.2
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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.
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Tetrahedron
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Welch, J.T.1
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4
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0027432004
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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.
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(1993)
Tetrahedron
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Resnati, G.1
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5
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0023237559
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Wiley Interscience, New York
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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.
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(1991)
Fluorine in Bioorganic Chemistry
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Welch, J.T.1
Eswarakrishnan, S.2
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6
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0023237559
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Biomedical frontiers in fluorine chemistry
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ACS, Washington, DC. and references therein
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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.
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ACS Symposium Series
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Ojima, I.1
McCarthy, J.R.2
Welch, J.T.3
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8
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33847800447
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(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.
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Middleton, W.J.1
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0033230427
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(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.
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De Jonghe, S.1
Van Overmeire, I.2
Poulton, S.3
Hendrix, C.4
Busson, R.5
Van Calenbergh, S.6
De Keukeleire, D.7
Spiegel, S.8
Herdewijn, P.9
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Grée D.M., Kermarrec C.J.M., Martelli J.T., Grée R.L., Lellouche J.P., Toupet L.J. J. Org. Chem. 61:1996;1918-1919.
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Grée, D.M.1
Kermarrec, C.J.M.2
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Grée, R.L.4
Lellouche, J.P.5
Toupet, L.J.6
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Grée, R.5
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Grée D., Vallerie L., Grée R., Toupet L., Washington I., Pelicier J.-P., Villacampa M., Perez J.M., Houk K.N. J. Org. Chem. 66:2001;2374-2382.
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Grée, D.1
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Washington, I.5
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Villacampa, M.7
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18
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85031061809
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If heating is maintained for longer periods the decomposition of 1a starts, possibly by autocatalytic processes, affording unidentified compounds
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If heating is maintained for longer periods the decomposition of 1a starts, possibly by autocatalytic processes, affording unidentified compounds.
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19
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85031061912
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2 at room temperature to perform this Z to E isomerisation
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2 at room temperature to perform this Z to E isomerisation.
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