Nakamura Akira
School of Pharmaceutical Sciences, Kindai University.
Yakugaku Zasshi. 2023;143(2):105-110. doi: 10.1248/yakushi.22-00154.
Chalcones are easily accessible synthetic building blocks that are used in various heterocyclic syntheses. The rearrangement reaction using an oxidant is a characteristic conversion of chalcones, but applications to organic synthesis have been limited. Here, the development of a new method for synthesizing 3-acylindoles and azaisoflavones using a chalcone rearrangement strategy with hypervalent iodine reagents was described. Furthermore, the obtained new insight was applied to the selective synthesis of two benzofuran isomers from 2-hydroxychalcone derivatives and have demonstrated this method to the synthesis of the natural product, puerariafuran.
查尔酮是易于获得的合成砌块,用于各种杂环合成。使用氧化剂的重排反应是查尔酮的一种特征性转化,但在有机合成中的应用一直有限。在此,描述了一种使用高价碘试剂的查尔酮重排策略合成3-酰基吲哚和氮杂异黄酮的新方法。此外,将获得的新见解应用于从2-羟基查尔酮衍生物选择性合成两种苯并呋喃异构体,并已证明该方法可用于天然产物葛根呋喃的合成。