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3
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0030885273
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(a) Marais A. D., Firth, J. C., Bateman, M. E., Byrnes P, Martens, C., and Mountney, J. -Arteriosclerosis, Thrombosis, and Vascular Biology 17: 1527 (1997), and references therein.
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Marais, A.D.1
Firth, J.C.2
Bateman, M.E.3
Byrnes, P.4
Martens, C.5
Mountney, J.6
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4
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(b) Alaupovic, P., Heinonen, T, Shurzinske, L., and Black, D. M. - Atherosclerosis. 133: 123 (1997).
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Atherosclerosis
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Alaupovic, P.1
Heinonen, T.2
Shurzinske, L.3
Black, D.M.4
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5
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18544412108
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(a) Bertolini, S., Bittolo-Bon, G., Malcolm-Campbell, L., Farnier, M., Langan, J., Mahla, G., Pauciullo, P., Sirtori, C., Egros, F., Fayyad, R., and Nawrocki, J. W. - Atherosclerosis 130: 191 (1997).
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Atherosclerosis
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Bertolini, S.1
Bittolo-Bon, G.2
Malcolm-Campbell, L.3
Farnier, M.4
Langan, J.5
Mahla, G.6
Pauciullo, P.7
Sirtori, C.8
Egros, F.9
Fayyad, R.10
Nawrocki, J.W.11
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6
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0031195278
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(b) Dart, A., Jerums, G., Nicholson, G., D'Emden, M., Hamilton-Craig, I., Tallis, G., Best, J., West, M., Sullivan, D., Bracs, P., and Black, D. Am. J. Cardiol. 80: 39 (1997).
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Am. J. Cardiol.
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Dart, A.1
Jerums, G.2
Nicholson, G.3
D'Emden, M.4
Hamilton-Craig, I.5
Tallis, G.6
Best, J.7
West, M.8
Sullivan, D.9
Bracs, P.10
Black, D.11
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7
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0030972431
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Kelleck, K. A., Burns, K., McAndrew E., Haberl, E., Hook, N, and Ellis, A.K. - Formulary 32: 352 (1997).
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(1997)
Formulary
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Kelleck, K.A.1
Burns, K.2
McAndrew, E.3
Haberl, E.4
Hook, N.5
Ellis, A.K.6
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9
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0026559054
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(a) Brower, P. L., Butler, D. E., Deering, C. F., Le, T. V., Millar, A., Nanninga, T. N., and Roth, B. D. - Tetrahedron Lett. 33: 2279 (1992).
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(1992)
Tetrahedron Lett.
, vol.33
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Brower, P.L.1
Butler, D.E.2
Deering, C.F.3
Le, T.V.4
Millar, A.5
Nanninga, T.N.6
Roth, B.D.7
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10
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0026504865
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(b) Baumann, K.L., Butler, D.E., Deering, C.F., Mennen, K.E., Millar, A., Nanninga, T.N., Palmer, C.W., and Roth, B.D. - ibid. 33: 2283 (1992);
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(1992)
Tetrahedron Lett.
, vol.33
, pp. 2283
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Baumann, K.L.1
Butler, D.E.2
Deering, C.F.3
Mennen, K.E.4
Millar, A.5
Nanninga, T.N.6
Palmer, C.W.7
Roth, B.D.8
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11
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85167467263
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U.S. Patent 5,149,837, Sept. 22, 1992
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Butler, D. E., Deering, C. F., Millar, A., Nanningar, T. N., and Roth, B. D. - U.S. Patent 5,149,837, Sept. 22, 1992).
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Butler, D.E.1
Deering, C.F.2
Millar, A.3
Nanningar, T.N.4
Roth, B.D.5
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12
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85167473303
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note
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In cold runs, the E- and Z-components were separated by silica gel column chromatography (elution with hexane:dichloromethane:EtOAc/9:1:1). TLC (silica gel, pentane:ether/2:1): E-isomer, Rf 0.52; Z-isomer, Rf 0.31. The configuration of the Z-isomer, crystals from ethyl acetate-cyclohexane, was established by single crystal X-ray crystallography. The Z-isomer is favored thermodynamically and the E-isomer is favored kinetically during synthesis.
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14
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85167477963
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note
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-1, log ε = 4.33, and is 247 nm in the mobile phase under HPLC conditions. Chemical purity by HPLC is defined as purity by area normalization at a chosen wavelength (e.g., 254 nm for 15, as specified for purity determination of the drug), generally near the absorption maximum with consideration being given to the the absorption characteristics of the impurities. During melting point determination (glass capillary, oil bath), atorvastatin, being a calcium salt, decomposed (shrinking, then expanding, and finally melting) over a wide temperature range of approximately 160 to 240 °C.
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15
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0027502918
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Hurley, T. R., Colson, C. E., Clipper, S. A., Uhlendorf, S. E., and Reily, M. D. - Tetrahedron 49: 1979 (1993).
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(1993)
Tetrahedron
, vol.49
, pp. 1979
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Hurley, T.R.1
Colson, C.E.2
Clipper, S.A.3
Uhlendorf, S.E.4
Reily, M.D.5
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