Palladium-catalyzed C-H bond activation and decarboxylation for the assembly of indolo[1,2-f]phenanthridine.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Xiaobing Liu, Yong-Liang Ban, Yanjie Liu, Mengdie Zhuang, Yao Zhou
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引用次数: 0

Abstract

A direct and convenient strategy for the assembly of indolo[1,2-f]phenanthridine via a Pd-catalyzed tandem cyclization reaction is presented. The current strategy delivers a range of indolo[1,2-f]phenanthridine derivatives by utilizing readily available 1-(2-iodophenyl)-1H-indole and commercially available o-bromobenzoic acids as the starting materials. The reaction features the formation of two C-C bonds through Pd-catalyzed C-H bond activation and decarboxylation.

钯催化 C-H 键活化和脱羧以组装吲哚并[1,2-f]菲啶。
本文介绍了一种通过 Pd 催化的串联环化反应组装吲哚并[1,2-f]菲啶的直接而方便的策略。目前的策略利用现成的 1-(2-碘苯基)-1H-吲哚和市售的邻溴苯甲酸作为起始原料,提供了一系列吲哚并[1,2-f]菲啶衍生物。该反应的特点是通过钯催化 C-H 键活化和脱羧形成两个 C-C 键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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