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2) affording the corresponding trimethylsilyl cyanohydrin.
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22
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34548194742
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note
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When the residue of the reaction (see ref. 11) was treated with HCl 1 N (2 ml) in acetonitrile (2 ml) at 0 °C for a few minutes after usual work-up the trimethylsilyl ether was quantitatively converted into corresponding cyanohydrins (see Scheme 1).
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