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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >EFFICIENT ORGANOCATALYTIC MICHAEL ADDITION REACTION OF β-KETOESTERS UNDER HIGH PRESSURE
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EFFICIENT ORGANOCATALYTIC MICHAEL ADDITION REACTION OF β-KETOESTERS UNDER HIGH PRESSURE

机译:高压下β-酮酯的有效有机催化迈克尔加成反应

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摘要

The Michael addition reaction of β-ketoesters was efficiently promoted by a cooperative dual catalyst system composed by DMAP and thiourea A under high-pressure conditions (0.8 GPa) in toluene. The expected relatively congested adducts of 1,5-dicarbonyl compounds were prepared in high to excellent yield.
机译:DMAP和硫脲A在高压条件下(0.8 GPa)在甲苯中组成的双催化协同体系有效地促进了β-酮酸酯的迈克尔加成反应。以高至优异的产率制备了预期的相对拥挤的1,5-二羰基化合物的加合物。

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