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4) and evaporated under reduced pressure to give the crude product, which upon recrystallisation from EtOH yielded the desired compound as colourless needles (1.123 g, 91%)
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4) and evaporated under reduced pressure to give the crude product, which upon recrystallisation from EtOH yielded the desired compound as colourless needles (1.123 g, 91%).
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3 aqueous solution (1 ml) was added. The mixture was stirred for 5 min at room temperature, filtered through a pad of alumina, washed with toluene (3×20 ml) and evaporated under reduced pressure to give the desired compound as white solids (2.384 g, 98%). This and all the other compounds given in Table 2 have been characterised by NMR, MS and elemental analysis or by comparison with authentic samples
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3 aqueous solution (1 ml) was added. The mixture was stirred for 5 min at room temperature, filtered through a pad of alumina, washed with toluene (3×20 ml) and evaporated under reduced pressure to give the desired compound as white solids (2.384 g, 98%). This and all the other compounds given in Table 2 have been characterised by NMR, MS and elemental analysis or by comparison with authentic samples.
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