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首页> 外文期刊>Organic letters >Synthesis of 7,7′-Dihydroxy-8,8′-biquinolyl (azaBINOL) via Pd-catalyzed directed double C-H functionalization of 8,8′-biquinolyl: Emergence of an atropos from a tropos state
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Synthesis of 7,7′-Dihydroxy-8,8′-biquinolyl (azaBINOL) via Pd-catalyzed directed double C-H functionalization of 8,8′-biquinolyl: Emergence of an atropos from a tropos state

机译:通过Pd催化的8,8'-联喹啉基的双C-H官能化合成7,7'-二羟基-8,8'-联喹啉基(azaBINOL):从对位状态出现atropos

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摘要

7,7′-Dihydroxy-8,8′-biquinolyl (azaBINOL) was prepared from 2-chloroaniline in four steps: (1) the Skraup reaction, (2) Ni-catalyzed reductive coupling of 8-chloroquinoline, (3) Pd(II)-catalyzed double C-H functionalization of 8,8′-biquinolyl mediated by PhI(OAc)_2, and (4) saponification. During the third step, an axially chiral (atropos type) biaryl molecule was directly generated from an essentially achiral (tropos type) biaryl starting material.
机译:由4-氯苯胺分四个步骤制得7,7'-二羟基-8,8'-联喹啉基(azaBINOL):( 1)Skraup反应;(2)Ni催化的8-氯喹啉还原偶联;(3)Pd (II)催化PhI(OAc)_2介导的8,8'-联喹啉基的双CH功能化,以及(4)皂化作用。在第三步骤中,从基本非手性(对位型)联芳基起始原料直接生成轴向手性(对位型)联芳基分子。

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