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Synthesis 2020; 52(12): 1833-1840
DOI: 10.1055/s-0039-1691740
DOI: 10.1055/s-0039-1691740
paper
Synthesis of 2,4-Diarylquinoline Derivatives via Chloranil-Promoted Oxidative Annulation and One-Pot Reaction
The authors are grateful to the Natural Science Foundation of China (21602197) and the Natural Science Foundation of Zhejiang Province (LY18B020018).Further Information
Publication History
Received: 24 December 2019
Accepted after revision: 06 February 2020
Publication Date:
24 February 2020 (online)
Abstract
An oxidative annulation for the synthesis of 2,4-diarylquinolines from o-allylanilines is disclosed that uses recyclable reagent Chloranil as the oxidant. The corresponding products are obtained in moderate to excellent yields. Furthermore, a one-pot access to 2,4-diarylquinolines from easily available anilines and 1,3-diarylpropenes is described as a highly atom-efficient protocol that involves oxidative coupling, rearrangement, and oxidative annulation.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0039-1691740.
- Supporting Information
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