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首页> 外文期刊>Journal of the Chemical Society, Perkin Transactions 1 >An efficient synthesis of the four mono methylated isomers of (+)-catechin including the major metabolites and of some dimethylated and trimethylated analogues through selective protection of the catechol ring
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An efficient synthesis of the four mono methylated isomers of (+)-catechin including the major metabolites and of some dimethylated and trimethylated analogues through selective protection of the catechol ring

机译:通过选择性保护邻苯二酚环,可有效合成(+)-儿茶素的四种单甲基化异构体,包括主要代谢物以及一些二甲基化和三甲基化类似物

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摘要

The four monomethylated isomers of (+)-catechin in positions 3', 4', 5 and 7, two dimethylated derivatives, the 5,7-dimethylcatechin and the 3',4'-dimethylcatechin and two trimethylated isomers of (+)-catechin in positions 3',5,7 and 4', 5, 7 were synthesized by a new method based on successive and selective protections of the various phenol functions present on (+)-catechin. The key step was the selective protection of the catechol ring with dichlorodiphenylmethane and di-tert-butyldichlorosilane. [References: 94]
机译:(+)-儿茶素在位置3',4',5和7中的四个单甲基化异构体,两个二甲基化衍生物,5,7-二甲基儿茶素和3',4'-二甲基儿茶素以及两个(+)-三甲基化异构体基于对(+)-儿茶素上存在的各种酚官能团的连续和选择性保护,通过新方法合成了3',5、7和4',5、7位的儿茶素。关键步骤是用二氯二苯甲烷和二叔丁基二氯硅烷选择性保护邻苯二酚环。 [参考:94]

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