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首页> 外文期刊>Organic letters >Regioselective Synthesis of Dihydrothiophenes and Thiophenes via the Rhodium-Catalyzed Transannulation of 1,2,3-Thiadiazoles with Alkenes
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Regioselective Synthesis of Dihydrothiophenes and Thiophenes via the Rhodium-Catalyzed Transannulation of 1,2,3-Thiadiazoles with Alkenes

机译:铑催化1,2,3-噻二唑与烯烃的铑催化跨环氧化反应选择性合成二氢噻吩和噻吩

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摘要

A method for the regioselective synthesis of a wide range of dihydrothiophenes was developed from the rhodium catalyzed transannulation of 1,2,3-thiadiazoles with aliphatic, aromatic, and heteroaromatic alkenes. Tandem rhodium-catalyzed transannulation of 1,2,3-thiadiazoles with alkenes followed by 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) oxidation was also demonstrated for the one-pot regioselective synthesis of various thiophenes. Advantages of the present method include a broad substrate scope, wide functional group compatibility, and high regioselectivity.
机译:由铑催化的1,2,3-噻二唑与脂族,芳族和杂芳族烯烃的环转移反应,开发了一种区域选择性合成多种二氢噻吩的方法。还证明了用铑进行的1,2,3-噻二唑与烯烃的串联铑催化转环,然后进行2,3-二氯-5,6-二氰基-1,4-苯醌(DDQ)氧化,可用于多种反应物的一锅区域选择性合成。噻吩。本方法的优点包括广泛的底物范围,广泛的官能团相容性和高区域选择性。

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