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2O as eluent to give the corresponding ketene selenothioacetals 3.
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All new compounds gave satisfactory spectral and microanalytical data.
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The high reactivity of the ammonium eneselenolate 2a toward alkyl halides is in sharp contrast to the reactivity of lithium eneselenolates generated from 1a and LDA. The methylation of lithium eneselenolates gave 3a only in low yields.
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