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Pd(0)-Catalyzed Tandem One-Pot Reaction of Biphenyl Ketones/Aldehydes to the Corresponding Di-substituted Aryl Olefins
Synthesis of di-substituted aryl olefins via a Pd(0)-catalyzed cross-coupling reaction of biphenyl ketones/alde- hydes, tosylhydrazide, and aryl bromides (or benzyl halides) was developed. This methodology was achieved by one-pot two-step reactions involving the preparation of N-tosylhydrazones by r...
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Published in: | 中国化学:英文版 2017, Vol.35 (7), p.1141-1148 |
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container_title | 中国化学:英文版 |
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creator | Yang Liu Ping Liu Yan Liu Yu Wei |
description | Synthesis of di-substituted aryl olefins via a Pd(0)-catalyzed cross-coupling reaction of biphenyl ketones/alde- hydes, tosylhydrazide, and aryl bromides (or benzyl halides) was developed. This methodology was achieved by one-pot two-step reactions involving the preparation of N-tosylhydrazones by reacting tosylhydrazide with biphenyl ketones/aldehydes, followed by coupling with aryl bromides (or benzyl halides) in the presence of Pd(PPh3)4 and lithium t-butoxide to produce various di-substituted aryl olefins in moderate to good yields. |
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subjects | 串联 二取代 交叉偶联反应 催化 反应合成 联苯 醛 |
title | Pd(0)-Catalyzed Tandem One-Pot Reaction of Biphenyl Ketones/Aldehydes to the Corresponding Di-substituted Aryl Olefins |
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