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The ene product indicated the presence of one major diastereomer, however, efforts were not made to separate or assign the configuration at the newly introduced stereogenic center of the major isomer since it was to be destroyed subsequently.
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31
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38949092598
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note
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2O followed by esterification. Clear differences were observed in the chemical shifts for methylene protons of the Mom group; in the ester derived from 17 they resonate at δ 4.43 and 4.39, and at δ 4.6 and 4.5 in the ester derived from the epimer of 17.
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0035793850
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l-Selectride stereoselectively affords threo 1,2-diol derivatives upon reducing derivatives of α-hydroxy ketones, refer:
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