Regioselective Synthesis of 2-Substituted indoles from Benzotriazoles and Alkynes by Photoinitiated Denitrogenation

被引:54
|
作者
Teders, Michael [1 ]
Pitzer, Lena [1 ]
Buss, Stefan [1 ]
Glorius, Frank [1 ]
机构
[1] Westfal Wilhelms Univ Munster, Inst Organ Chem, Corrensstr 40, D-48149 Munster, Germany
来源
ACS CATALYSIS | 2017年 / 7卷 / 06期
关键词
photocatalysis; robustness screen; regioselective; indoles; benzotriazoles; mechanism-based screening; NONREARRANGED MONOTERPENOID UNIT; VISIBLE-LIGHT; PHOTOREDOX CATALYSIS; ROBUSTNESS SCREEN; MASS-SPECTROMETRY; ORGANIC-SYNTHESIS; INTERNAL ALKYNES; ALKALOIDS; PHOTOCATALYSIS; CYCLIZATION;
D O I
10.1021/acscatal.7b01025
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Herein, we describe a photoinitiated and regioselective synthesis of 2-substituted indoles under mild reaction conditions. This biologically privileged scaffold was accessed in good yields from N-aroylbenzotriazoles, a quencher class previously identified using our mechanism-based luminescence screening, and terminal alkynes in the presence of a photocatalyst and blue light irradiation. This straightforward protocol displays a broad substrate scope and functional group tolerance. Furthermore, the mildness and robustness of the reaction were assessed by the application of an additive-based robustness screen. The determination of the reaction quantum yield and Stern-Volmer studies support the proposed photo initiated radical chain mechanism.
引用
收藏
页码:4053 / 4056
页数:4
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