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8
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51349143217
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Mileni M., Johnson D.S., Wang Z., Everdeen D.S., Liimatta M., Pabst B., Bhattacharya K., Nugent R.A., Kamtekar S., Cravatt B.F., Ahn K., and Stevens R.C. Proc. Natl. Acad. Sci. U.S.A. 105 (2008) 12820
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Stevens, R.C.12
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9
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64749114255
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Bhattacharya, K.14
Zhang, Y.15
Swaney, S.16
Becelaere, K.V.17
Stevens, R.C.18
Cravatt, B.F.19
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10
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65349167368
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Johnson D.S., Ahn K., Kesten S., Lazerwith S.E., Song Y., Morris M., Fay L., Gregory T., Stiff C., Dunbar J.B., Liimatta M., Beidler D., Smith S., Nomanbhoy T.K., and Cravatt B.F. Bioorg. Med. Chem. Lett. 19 (2009) 2865
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Fay, L.7
Gregory, T.8
Stiff, C.9
Dunbar, J.B.10
Liimatta, M.11
Beidler, D.12
Smith, S.13
Nomanbhoy, T.K.14
Cravatt, B.F.15
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12
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70349224706
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note
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Compound 2 was prepared from 3-hydroxy methylbenzoate in four steps.
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13
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70349219107
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WO 9318029 A1, 1993
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Matassa, V. G. WO 9318029 A1, 1993.
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Matassa, V.G.1
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14
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70349222059
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note
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Olefin separation condition: Set up AI 30×250 mm chiral column elute with 20% EtOH and 80% CO2. Sample dissolved in 20 mL EtOH, 25 mg/mL, 1 mL per inject. The olefin stereochemistry was assigned by 2D NMR.
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-
-
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15
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70349221966
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Compound 10 was prepared as described in WO 08047229, 2008
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Compound 10 was prepared as described in WO 08047229, 2008.
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16
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3543047335
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Corley E.G., Conrad K., Murry J.A., Savarin C., Holko J., and Boice G. J. Org. Chem. 69 (2004) 5120
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(2004)
J. Org. Chem.
, vol.69
, pp. 5120
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Corley, E.G.1
Conrad, K.2
Murry, J.A.3
Savarin, C.4
Holko, J.5
Boice, G.6
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18
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70349221967
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note
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Compound 16 was prepared through the similar sequence as compound 9.
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-
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19
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70349221876
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note
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The Pfizer Institutional Animal Care and Use Committee reviewed and approved the animal use in these studies. The animal care and use program is fully accredited by the Association for Assessment and Accreditation of Laboratory Animal Care, International.
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