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1
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0009470488
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Leznoff, C. C. Acc. Chem. Res. 1978, 11, 327-333, McKillop, A.; Young, D. W. Synthesis 1979, 401-422 and 481-500. Akelah, A.; Sherrington, D. C. Chem. Rev. 1981, 81, 557-587. Früchtel, J. S.; Jung, G. Angew. Chem., Int. Ed. Engl. 1996, 35, 17-42. Shuttleworth, S. J.; Allin, S. M.; Sharma, P. K.; Synthesis 1997, 1217-1239. Drewry, D. H.; Coe, D. M.; Poon, S. Med. Chem. Rev. 1999, 2, 97-148. Shuttleworth, S. J.; Allin, S. M.; Wilson, R. D.; Nasturica, D. Synthesis 2000, 1035-1074. Ley, S. V.; Baxendale, I. R.; Bream, R. N.; Jackson, P. S.; Leach, A. G.; Longbottom, D. A.; Nesi, M.; Scott, J. S.; Storer, R. I.; Taylor, S. J. J. Chem. Soc., Perkin. Trans. 1 2000, 3815.
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McKillop, A.1
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0002297755
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33748237769
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0033052277
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41
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0001505956
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See, for example: Garner, P.; Anderson, J. T.; Dey, S.; Youngs, W. J.; Galat, K.J. Org. Chem. 1998, 63, 5732-5733. Garner, P.; Anderson, J. T. Org. Lett. 1999, 1, 1057-1059. Ollivier, C.; Renaud, P. Angew. Chem., Int. Ed. 2000, 39, 925-928.
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42
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See, for example: Garner, P.; Anderson, J. T.; Dey, S.; Youngs, W. J.; Galat, K.J. Org. Chem. 1998, 63, 5732-5733. Garner, P.; Anderson, J. T. Org. Lett. 1999, 1, 1057-1059. Ollivier, C.; Renaud, P. Angew. Chem., Int. Ed. 2000, 39, 925-928.
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46
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0042122007
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note
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2, C, 46.63; H, 3.20; N, 4.94; S, 22.64. Found C, 46.50; H. 3.15; N, 4.77.
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47
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0014772602
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0043123937
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note
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2 was bubbled through the solution. After filtration, the amount of t-BuBr formed (approximatively 30 mg, 92% yield) was determined by GC analysis. Alternatively, evaporation of the solvent gave products 8b-d. The GC analysis of t-BuBr can also be used as an indirect method to evaluate the loading of the resin.
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50
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0032575141
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0041621140
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note
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-1.
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52
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0000217511
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Following the preparation described in the literature (Hartung, J.; Hiller, M.; Schmidt, P. Chem. Eur. J. 1996, 2, 1014-1023), 15 and 16 were always obtained as a mixture of diastereoisomers after two chromatographic separations.
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