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Beight, D. W.; Mehdi, S.; Koehl, J. R.; Flynn, G.A. Presented in preliminary form at the 203rd National Meeting of the American Chemical Society, Washington, DC, August 1992.
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0009623344
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San Francisco, CA, April
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(a) Flynn. G. A.; Beight, D. W.; Warshawsky, A. M.; Burkholder, T. P.; Mehdi, S.; Giroux, E. L.; Dage, R. C. Presented at the 203rd National Meeting of the American Chemical Society, San Francisco, CA, April 1992.
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Mehdi, S.5
Giroux, E.L.6
Dage, R.C.7
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(b) Flynn, G. A.; Beight, D. W.; Mehdi, S.; Koehl, J. R.; Giroux, E. L.; French, J. F.; Hake, P. W.; Dage, R. C. J. Med. Chem. 1993, 36, 2420.
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Flynn, G. A.; Beight, D. W.; Huber, E. W.; Bey, P. Tetrahedron Lett. 1990, 31, 815.
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85030271844
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World Patent WO 91/09840
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(a) Neustadt, B. World Patent WO 91/09840.
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Neustadt, B.1
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85030275150
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US Patent 5, 252, 601, 1993
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(b) Flynn G. A.; Beight, D. W.; US Patent 5, 252, 601, 1993.
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Flynn, G.A.1
Beight, D.W.2
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For the preparation of 3a see: Tomiyama, T.; Wakabayashi, S.; Yokata, M. J. Med. Chem. 1989, 32, 1988.
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0000969622
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Turchaninova, L.P.; Voronkov, M. G.; Shipov, A. G.; Korchevin, N. A.; Baukov, Y. I.; Deryagina, E. N. Zh. Obshch. Khim. 1989, 59, 722. Experimental procedure for preparation of chloromethyl sulfides: To a mixture of 15.9 mL (125 mmol) TMSCl and 1.5 g (50 mmol) paraformaldehyde at 0 °C was added 7.0 mL (50 mmol) para-methoxybenzyl mercaptan. The mixture was stirred 2 h while warming to 20 °C, then distilled, bp 90-96 °C/0.1 torr. Yield: 3.5 g (34%).
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Zh. Obshch. Khim.
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Turchaninova, L.P.1
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Deryagina, E.N.6
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17
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85030274056
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See ref 10. bp 80-86 °C/75 torr. Yield: 60%
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See ref 10. bp 80-86 °C/75 torr. Yield: 60%.
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18
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0027467360
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33646274424
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Baumgarten, H. E., Ed.; Wiley: New York
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For the preparation of 6e see: (a) Pearlman W. M. Org. Synth. Collect. Vol. 5; Baumgarten, H. E., Ed.; Wiley: New York, 1973; p 760.
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23
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French, J. F.; Flynn, G. A.; Giroux, E. L.; Mehdi, S.; Anderson, B.; Beach, D. C.; Koehl, J. R.; Dage, R. C. J. Pharmacol. Exp. Ther. 1994, 268, 180.
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Mehdi, S.4
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Koehl, J.R.7
Dage, R.C.8
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24
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85030279548
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The enantiomers of 1b were separated on a cyclodextrin column. The (+) enantiomer eluted first and was purified to ∼96% ee. The (-) enantiomer was purified to ∼86% ee
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The enantiomers of 1b were separated on a cyclodextrin column. The (+) enantiomer eluted first and was purified to ∼96% ee. The (-) enantiomer was purified to ∼86% ee.
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25
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0023200033
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Benchetrit, T.; Fournié-Zaluskie, M. C.; Roques, B. P. Biochem. Biophys. Res. Commun. 1987, 147, 1034.
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Roques, B.P.3
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