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一种构建A 型酰基间苯三酚全功能化双环骨架的短仿生方法。

A short biomimetic approach to the fully functionalized bicyclic framework of type A acylphloroglucinols.

作者信息

Couladouros Elias A, Dakanali Marianna, Demadis Konstantinos D, Vidali Veroniki P

机构信息

Chemical Laboratories, Agricultural University of Athens, Iera Odos 75, GR-11855 Athens, Greece.

出版信息

Org Lett. 2009 Oct 1;11(19):4430-3. doi: 10.1021/ol901781n.

Abstract

A biomimetic approach toward type A polyprenylated acylphloroglucinols (PPAPs) is described. The method is based on a C-alkylation-cation cyclization reaction sequence, leading to a convenient buildup of molecular complexity, employing the simple and readily available deoxycohumulone and an appropriately functionalized hydroxy halide. Thus, a versatile construction of the fully functionalized bicyclic framework of type A PPAPs (5) was achieved.

摘要

描述了一种用于 A 型多异戊烯基化酰基间苯三酚(PPAPs)的仿生方法。该方法基于碳烷基化-阳离子环化反应序列,利用简单易得的脱氧香豆酮和适当官能化的卤代醇,方便地构建分子复杂性。因此,实现了 A 型 PPAPs(5)全官能化双环骨架的通用构建。

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