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首页> 外文期刊>Journal of Organometallic Chemistry >Base free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: A novel synthesis of substituted aryl ketones
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Base free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: A novel synthesis of substituted aryl ketones

机译:钠(芳基Trihydroxyborate)盐的基础游离铃木酰化反应:一种新的取代芳基酮的合成

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摘要

The first simple and efficient base free Pd(PPh3)(4) catalysed synthesis of substituted aryl ketones from acyl chlorides and easily accessible sodium aryl trihydroxyborate salts in aqueous toluene is reported. The reaction conditions appeared versatile and tolerable to a variety of functional groups including, CF3, OMe, SMe, Br, NO2, F, OH and NH2 furnishing 25 examples of substituted aryl ketones in isolated yields of up to 96% in 24 h. Beside the high purity, the ease and convenience of the isolation compared to boronic acids, sodium aryl trihydroxyborate salts could be used subsequently without the addition of excess amount of an activator and are more user-friendly in terms of the use of accurate reaction stoichiometry. (C) 2017 Elsevier B.V. All rights reserved.
机译:据报道,第一简单且有效的基础免疫Pd(PPH3)(4)催化合成来自酰氯和易于接近的甲苯含水甲苯易于偏转的芳基Trihydroxyborate盐。 对反应条件看似多功能并且可容许的各种官能团,包括CF 3,OME,中小企业,Br,No2,F,OH和NH 2家庭24小时的取代的芳基酮的实施例,其24小时高达96%。 除了高纯度,与硼酸相比,隔离的缓和和便利性,随后可以使用芳基三羟基硼酸钠盐,而不会加入过量的活化剂,并且在使用精确反应化学计量方面更用户友好。 (c)2017年Elsevier B.V.保留所有权利。

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