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0011723016
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4), concentrated and purified via flash chromatography to yield 4.1 g (84%) of product as a viscous oil.
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19
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85087578310
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note
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3 (5%) followed by brine. The reaction was concentrated and purified via flash chromatography to give 0.18 g of oxazinone as a colorless solid.
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20
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0029878786
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1 receptor antagonists see: (a) J. J. Hale, S. G. Mills, M. MacCoss, S. K. Shah, H. Qi, D. J. Mathre, M. A. Cascieri, S. Sadowski, C. D. Strader, D. E. MacIntyre, and J. M. Metzger, J. Med. Chem., 1996, 39, 1760. (b) J. J. Hale, S. G. Mills, M. MacCoss, P. E. Finke, M. A. Cascieri, S. Sadowski, E. Ber, G. G. Chicchi, M. Kurtz, J. Metzger, G. Eiermann, N. N. Tsou, F. D. Tatersall, M. N. J. Rupniak, A. R. Williams, W. Rycroft, R. Hargreaves, and D. E. Maclntyre, J. Med. Chem., 1998, 41, 4607. (c) C. J. Cowden, R. D. Wilson, B. C. Bishop, I. F. Cottrell, A. J. Davies, and U.-H. Dolling, Tetrahedron Lett., 2000, 41, 8661. (d) D. J. Wallace, J. M. Goodman, D. J. Kennedy, A. J. Davies, C. J. Cowden, M. S. Ashwood, I. F. Cottrell, U.-H. Dolling, and P. J. Reider, Org. Lett., 2001, 3, 671.
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Hale, J.J.1
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Strader, C.D.9
MacIntyre, D.E.10
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21
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15144354434
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1 receptor antagonists see: (a) J. J. Hale, S. G. Mills, M. MacCoss, S. K. Shah, H. Qi, D. J. Mathre, M. A. Cascieri, S. Sadowski, C. D. Strader, D. E. MacIntyre, and J. M. Metzger, J. Med. Chem., 1996, 39, 1760. (b) J. J. Hale, S. G. Mills, M. MacCoss, P. E. Finke, M. A. Cascieri, S. Sadowski, E. Ber, G. G. Chicchi, M. Kurtz, J. Metzger, G. Eiermann, N. N. Tsou, F. D. Tatersall, M. N. J. Rupniak, A. R. Williams, W. Rycroft, R. Hargreaves, and D. E. Maclntyre, J. Med. Chem., 1998, 41, 4607. (c) C. J. Cowden, R. D. Wilson, B. C. Bishop, I. F. Cottrell, A. J. Davies, and U.-H. Dolling, Tetrahedron Lett., 2000, 41, 8661. (d) D. J. Wallace, J. M. Goodman, D. J. Kennedy, A. J. Davies, C. J. Cowden, M. S. Ashwood, I. F. Cottrell, U.-H. Dolling, and P. J. Reider, Org. Lett., 2001, 3, 671.
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Hale, J.J.1
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Ber, E.7
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Tatersall, F.D.13
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Rycroft, W.16
Hargreaves, R.17
Maclntyre, D.E.18
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22
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0034727282
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1 receptor antagonists see: (a) J. J. Hale, S. G. Mills, M. MacCoss, S. K. Shah, H. Qi, D. J. Mathre, M. A. Cascieri, S. Sadowski, C. D. Strader, D. E. MacIntyre, and J. M. Metzger, J. Med. Chem., 1996, 39, 1760. (b) J. J. Hale, S. G. Mills, M. MacCoss, P. E. Finke, M. A. Cascieri, S. Sadowski, E. Ber, G. G. Chicchi, M. Kurtz, J. Metzger, G. Eiermann, N. N. Tsou, F. D. Tatersall, M. N. J. Rupniak, A. R. Williams, W. Rycroft, R. Hargreaves, and D. E. Maclntyre, J. Med. Chem., 1998, 41, 4607. (c) C. J. Cowden, R. D. Wilson, B. C. Bishop, I. F. Cottrell, A. J. Davies, and U.-H. Dolling, Tetrahedron Lett., 2000, 41, 8661. (d) D. J. Wallace, J. M. Goodman, D. J. Kennedy, A. J. Davies, C. J. Cowden, M. S. Ashwood, I. F. Cottrell, U.-H. Dolling, and P. J. Reider, Org. Lett., 2001, 3, 671.
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23
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0035826378
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1 receptor antagonists see: (a) J. J. Hale, S. G. Mills, M. MacCoss, S. K. Shah, H. Qi, D. J. Mathre, M. A. Cascieri, S. Sadowski, C. D. Strader, D. E. MacIntyre, and J. M. Metzger, J. Med. Chem., 1996, 39, 1760. (b) J. J. Hale, S. G. Mills, M. MacCoss, P. E. Finke, M. A. Cascieri, S. Sadowski, E. Ber, G. G. Chicchi, M. Kurtz, J. Metzger, G. Eiermann, N. N. Tsou, F. D. Tatersall, M. N. J. Rupniak, A. R. Williams, W. Rycroft, R. Hargreaves, and D. E. Maclntyre, J. Med. Chem., 1998, 41, 4607. (c) C. J. Cowden, R. D. Wilson, B. C. Bishop, I. F. Cottrell, A. J. Davies, and U.-H. Dolling, Tetrahedron Lett., 2000, 41, 8661. (d) D. J. Wallace, J. M. Goodman, D. J. Kennedy, A. J. Davies, C. J. Cowden, M. S. Ashwood, I. F. Cottrell, U.-H. Dolling, and P. J. Reider, Org. Lett., 2001, 3, 671.
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Wallace, D.J.1
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R. J. Alabaster, A. W. Gibson, S. A. Johnson, J. S. Edwards and I. F. Cottrell, Tetrahedron Asymmetry, 1997, 8, 447.
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