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金催化硫炔经非卡宾途径氧化生成苯硫基乙烯酮衍生物

Gold-Catalyzed Oxidation of Thioalkynes To Form Phenylthio Ketene Derivatives via a Noncarbene Route.

作者信息

Sharma Pankaj, Singh Rahulkumar Rajmani, Giri Sovan Sundar, Chen Liang-Yu, Cheng Mu-Jeng, Liu Rai-Shung

机构信息

Frontier Research Center on Fundamental and Applied Sciences of Matters, Department of Chemistry , National Tsing-Hua University , Hsinchu , Taiwan , Republic of China.

Department of Chemistry , National Cheng Kung University , Tainan 701 , Taiwan , Republic of China.

出版信息

Org Lett. 2019 Jul 19;21(14):5475-5479. doi: 10.1021/acs.orglett.9b01768. Epub 2019 Jul 5.

Abstract

Gold-catalyzed oxidations of thioalkynes with 8-methylquinoline oxides afford 2-phenylthioketenes that can be trapped efficiently with alcohols. The synthetic utility is manifested by terminal and internal thioalkynes over a wide scope, bearing esters, ketones, alkyl, and oxime substituents. Our density functional theory calculations suggest that gold-catalyzed oxidations of terminal and internal thioalkynes with 8-methylquinoline oxides generate gold-bound ketene intermediates without the intermediacy of α-oxo gold carbene.

摘要

金催化硫代炔烃与8-甲基喹啉氧化物的氧化反应可生成2-苯基硫代烯酮,该产物能与醇类有效捕获。末端和内端硫代炔烃在广泛范围内均有合成效用,带有酯基、酮基、烷基和肟取代基。我们的密度泛函理论计算表明,金催化末端和内端硫代炔烃与8-甲基喹啉氧化物的氧化反应会生成与金相连的烯酮中间体,而无需α-氧代金卡宾作为中间体。

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