Chinese Journal of Organic Chemistry >
Aniline-Promoted Synthesis of Isobenzofuranone Derivatives
Received date: 2018-06-21
Revised date: 2018-07-16
Online published: 2018-07-24
Supported by
Project supported by the National Natural Science Foundation of China (Nos. 81430085, 81773562, 81703326), the National Key Research Program of Proteins (No. 2016YFA0501800), the Scientific Program of Henan Province (No. 182102310123), the China Postdoctoral Science Foundation (No. 2018M630840), the Open Project of Guangdong Provincial Key Laboratory of New Drug Screening (No. GDKLNDS-2018OF006), the Key Research Program of Higher Education of Henan Province (No. 18B350009), and the Undergraduate Innovation and Entrepreneurship Training Program of Zhengzhou University (No. 201810459101).
Isobenzofuranone derivatives are widely found in nature and have shown diverse biological activities. In this work, the aniline-promoted synthesis of isobenzofuranone derivatives starting from 2-carboxybenzaldehyde and substituted acetophenones under mild reaction conditions is reported. This method has broad substrate scope, high yields, and is operationally convenient, and therefore could serve as an attractive strategy for practical synthesis of isobenzofuranone derivatives.
Key words: isobenzofuranone derivatives; aniline; cascade reactions
Yuan Shuo , Wang Sixi , Chen Jinjie , Zhao Longfei , Yu Bin , Liu Hongmin . Aniline-Promoted Synthesis of Isobenzofuranone Derivatives[J]. Chinese Journal of Organic Chemistry, 2018 , 38(11) : 3009 -3015 . DOI: 10.6023/cjoc201806035
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