Abstract
ABSTRAC
Aryl nitriles react smoothly with sodium hydrogen selenide, itself prepared in situ from selenium and sodium borohydride, in ethanol to give the corresponding primary selenoamides in moderate to good yield.
ABSTRAC
Aryl nitriles react smoothly with sodium hydrogen selenide, itself prepared in situ from selenium and sodium borohydride, in ethanol to give the corresponding primary selenoamides in moderate to good yield.
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