1. Syntheses of α-Thio-β-dicarbonyl Compounds through Oxidative Coupling Reaction2. Microwave-Assisted Oxidative Cross-Coupling Reaction of Aldehydes with Thiols

碩士 === 國立中興大學 === 化學系所 === 103 === K2S2O8/I2 promoted C-S coupling reaction of β-diketone with disulfide has been described. The resulting α-thio-β-diketones compounds were obtained in good to excellent yields. Both diaryl and dialkyl disulfides are coupled well with a variety of β-diketones und...

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Main Authors: Yi-Wei Liu, 劉奕緯
Other Authors: Chin-Fa Lee
Format: Others
Language:zh-TW
Published: 2015
Online Access:http://ndltd.ncl.edu.tw/handle/38296283359536613383
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spelling ndltd-TW-103NCHU50650252016-08-15T04:17:57Z http://ndltd.ncl.edu.tw/handle/38296283359536613383 1. Syntheses of α-Thio-β-dicarbonyl Compounds through Oxidative Coupling Reaction2. Microwave-Assisted Oxidative Cross-Coupling Reaction of Aldehydes with Thiols 1.通過氧化耦合反應合成α-硫基-β-雙羰基化合物2.微波促進醛類與硫醇之交互耦合反應 Yi-Wei Liu 劉奕緯 碩士 國立中興大學 化學系所 103 K2S2O8/I2 promoted C-S coupling reaction of β-diketone with disulfide has been described. The resulting α-thio-β-diketones compounds were obtained in good to excellent yields. Both diaryl and dialkyl disulfides are coupled well with a variety of β-diketones under metal-free and solvent-free conditions. A very simple microwave-promoted synthesis of thioesters through the coupling of thiols and aldehydes under metal-free and solvent-free conditions was reported. This system shows good functional group tolerance, functional groups including bromo, iodo, nitrile, trifluoromethyl, thiophene and pyridine are all tolerated under the reaction conditions employed. Both aryl and alkyl thiols are coupled smoothly with a broad spectrum of aldehydes to afford the corresponding thioesters in good to excellent yields. Chin-Fa Lee 李進發 2015 學位論文 ; thesis 260 zh-TW
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description 碩士 === 國立中興大學 === 化學系所 === 103 === K2S2O8/I2 promoted C-S coupling reaction of β-diketone with disulfide has been described. The resulting α-thio-β-diketones compounds were obtained in good to excellent yields. Both diaryl and dialkyl disulfides are coupled well with a variety of β-diketones under metal-free and solvent-free conditions. A very simple microwave-promoted synthesis of thioesters through the coupling of thiols and aldehydes under metal-free and solvent-free conditions was reported. This system shows good functional group tolerance, functional groups including bromo, iodo, nitrile, trifluoromethyl, thiophene and pyridine are all tolerated under the reaction conditions employed. Both aryl and alkyl thiols are coupled smoothly with a broad spectrum of aldehydes to afford the corresponding thioesters in good to excellent yields.
author2 Chin-Fa Lee
author_facet Chin-Fa Lee
Yi-Wei Liu
劉奕緯
author Yi-Wei Liu
劉奕緯
spellingShingle Yi-Wei Liu
劉奕緯
1. Syntheses of α-Thio-β-dicarbonyl Compounds through Oxidative Coupling Reaction2. Microwave-Assisted Oxidative Cross-Coupling Reaction of Aldehydes with Thiols
author_sort Yi-Wei Liu
title 1. Syntheses of α-Thio-β-dicarbonyl Compounds through Oxidative Coupling Reaction2. Microwave-Assisted Oxidative Cross-Coupling Reaction of Aldehydes with Thiols
title_short 1. Syntheses of α-Thio-β-dicarbonyl Compounds through Oxidative Coupling Reaction2. Microwave-Assisted Oxidative Cross-Coupling Reaction of Aldehydes with Thiols
title_full 1. Syntheses of α-Thio-β-dicarbonyl Compounds through Oxidative Coupling Reaction2. Microwave-Assisted Oxidative Cross-Coupling Reaction of Aldehydes with Thiols
title_fullStr 1. Syntheses of α-Thio-β-dicarbonyl Compounds through Oxidative Coupling Reaction2. Microwave-Assisted Oxidative Cross-Coupling Reaction of Aldehydes with Thiols
title_full_unstemmed 1. Syntheses of α-Thio-β-dicarbonyl Compounds through Oxidative Coupling Reaction2. Microwave-Assisted Oxidative Cross-Coupling Reaction of Aldehydes with Thiols
title_sort 1. syntheses of α-thio-β-dicarbonyl compounds through oxidative coupling reaction2. microwave-assisted oxidative cross-coupling reaction of aldehydes with thiols
publishDate 2015
url http://ndltd.ncl.edu.tw/handle/38296283359536613383
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