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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >A CATALYTIC C-C BOND-FORMATION WITH MINIMAL USE OF PROTECTING GROUPS: CONSTRUCTION OF FUNCTIONALIZED ISOTETRONIC ACID DERIVATIVES
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A CATALYTIC C-C BOND-FORMATION WITH MINIMAL USE OF PROTECTING GROUPS: CONSTRUCTION OF FUNCTIONALIZED ISOTETRONIC ACID DERIVATIVES

机译:极少使用保护基的催化性C-C键形成:功能化的全同价酸衍生物的构建

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摘要

A catalytic method to construct multi-functionalized isotetronic acids was developed using cyclic hemiacetals and pyruvic acid derivatives as substrates. The key to success was the combination of catalytic amounts of iron(III) trifluoroacetate and 2-mercaptopyridine. A catalytic asymmetric variant was also developed using 6,6'-dimethoxy-binaphthyl phosphate instead of 2-mercaptopyridine.
机译:以环半缩醛和丙酮酸衍生物为底物,开发了一种催化方法,以构建多功能的等渗酸。成功的关键是催化量的三氟乙酸铁(III)和2-巯基吡啶的组合。还使用6,6'-二甲氧基-联萘磷酸酯代替2-巯基吡啶开发了催化不对称变体。

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