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In synthesis of anti- mold medicine preparation process of useful kiraru intermediate field

机译:在合成有用的基拉鲁中间体领域的抗霉菌药物制备过程中

摘要

(57) Abstract The manner which prepares the kiraru chemical compound formula (ii) is stated. Here, X1 and X2, becoming independent, is F or Cl, Y Cl and Br or is I. As for this manner, the triol formula (viii) (here, X1 and as for X2 defined first, as, is,) under catalytic converter existing after reacting with acetone, Cl2, the fact that it reacts with halogen or N-buromosukushinimido or N-yodosukushinimido which are chosen from Br2 or I2 is included.
机译:(57)<摘要>叙述了制备基拉鲁化学式(ii)的方法。此处,X 1 和X 2 变得独立,是F或Cl,Y Cl和Br或I。就这种方式而言,三醇式(viii)(这里,X 1 和X 2 首先定义为与丙酮Cl 2 反应后存在的催化转化器,它包括与卤素或选自Br 2 或I 2 的N-buromosukushinimido或N-yodosukushinimido反应的事实。

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