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Regio‐ and Diastereoselective KMnO4/RCO2H Mediated Acyloxyarylation of Chalcones – An Indirect α‐Arylation of Chalcones
European Journal of Organic Chemistry ( IF 2.8 ) Pub Date : 2020-03-27 , DOI: 10.1002/ejoc.201901647
Mehdi Adib 1 , Saideh Rajai-Daryasarei 1 , Rahim Pashazadeh 1 , Mohammad Mahdavi 2 , Mozhdeh Madadi 1 , Mehdi Jahani 1
Affiliation  

A manganese(VII)‐mediated regio‐ and diastereoselective acyloxyarylation of chalcones is unveiled. Heating a solution of a chalcone and an arylboronic acid in an aliphatic carboxylic acid at 80 °C for 1 h afforded the corresponding 1‐acyloxy‐3‐oxo‐1,2,3‐triarylpropanes in high yields. The β‐acyloxy‐α‐arylation/elimination sequence can be regarded as an indirect α‐arylation of chalcones.
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中文翻译:

区域和非对映选择性的KMnO4 / RCO2H介导的al的酰氧基化反应– al的间接α-芳基化反应

揭示了锰(VII)介导的查尔酮的区域和非对映选择性酰氧基化反应。将查尔酮和芳基硼酸在脂肪族羧酸中的溶液在80°C下加热1小时,可以高收率得到相应的1-酰氧基-3-氧代1,2,3-三芳基丙烷。β-酰氧基-α芳基化/消除序列可视为查耳酮的间接α芳基化。
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更新日期:2020-03-27
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