Chemistry Letters p. 403 - 406 (1986)
Update date:2022-08-12
Topics:
Suzuki, Hitomi
Inouye, Masahiko
Sodium telluride, prepared by heating tellurium and sodium hydride in a 1:2 molar ratio in dry N,N-dimethylformamide, readily debrominates a bromoacetic ester at low temperatures to generate an enolate anion, which undergoes a Reformatsky-type reaction with various non-enolizable aldehydes to give the corresponding α,β-unsaturated esters in good to moderate yields.Ketones remain almost unaffected under the same conditions.
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