A TfOH Catalyzed One-pot Synthesis of Aryl-Substituted Benzoquinones and Quinones via C-C Bond Formation

碩士 === 高雄醫學大學 === 醫藥暨應用化學系碩士班 === 103 === 。Substituted naphthoquinone and benzoquinone derivatives exist widely in nature and exhibit various important biological activities including antibiotic, antitumor, antidiabetic and inhibition of HIV-1 reverse transcriptase. Among these, the aryl substituted...

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Main Authors: Jia-Heng Jiang, 蔣佳恆
Other Authors: Jeh-Jeng Wang
Format: Others
Language:zh-TW
Published: 2015
Online Access:http://ndltd.ncl.edu.tw/handle/13452699380160562759
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spelling ndltd-TW-103KMC055370052016-08-15T04:17:23Z http://ndltd.ncl.edu.tw/handle/13452699380160562759 A TfOH Catalyzed One-pot Synthesis of Aryl-Substituted Benzoquinones and Quinones via C-C Bond Formation 藉由三氟甲磺酸催化與一鍋化進行&;#37260;類與苯胺類的碳-碳鍵合成 Jia-Heng Jiang 蔣佳恆 碩士 高雄醫學大學 醫藥暨應用化學系碩士班 103 。Substituted naphthoquinone and benzoquinone derivatives exist widely in nature and exhibit various important biological activities including antibiotic, antitumor, antidiabetic and inhibition of HIV-1 reverse transcriptase. Among these, the aryl substituted derivatives are of particular interest due to their presence in many natural products, such as belmacandaquinones and building blocks for many pharmaceuticals, natural products and dyes. By considering the importance of these aryl substituted benzoquinones and quinones, an acid catalyzed sequential one-pot approach was developed. This synthetic approach consists of oxidation of napthols/phenols to napthoquinone/benzoquinones followed by TfOH catalyzed arylation with electron rich arenes via C-C bond formation. Jeh-Jeng Wang 王志鉦 2015 學位論文 ; thesis 123 zh-TW
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language zh-TW
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sources NDLTD
description 碩士 === 高雄醫學大學 === 醫藥暨應用化學系碩士班 === 103 === 。Substituted naphthoquinone and benzoquinone derivatives exist widely in nature and exhibit various important biological activities including antibiotic, antitumor, antidiabetic and inhibition of HIV-1 reverse transcriptase. Among these, the aryl substituted derivatives are of particular interest due to their presence in many natural products, such as belmacandaquinones and building blocks for many pharmaceuticals, natural products and dyes. By considering the importance of these aryl substituted benzoquinones and quinones, an acid catalyzed sequential one-pot approach was developed. This synthetic approach consists of oxidation of napthols/phenols to napthoquinone/benzoquinones followed by TfOH catalyzed arylation with electron rich arenes via C-C bond formation.
author2 Jeh-Jeng Wang
author_facet Jeh-Jeng Wang
Jia-Heng Jiang
蔣佳恆
author Jia-Heng Jiang
蔣佳恆
spellingShingle Jia-Heng Jiang
蔣佳恆
A TfOH Catalyzed One-pot Synthesis of Aryl-Substituted Benzoquinones and Quinones via C-C Bond Formation
author_sort Jia-Heng Jiang
title A TfOH Catalyzed One-pot Synthesis of Aryl-Substituted Benzoquinones and Quinones via C-C Bond Formation
title_short A TfOH Catalyzed One-pot Synthesis of Aryl-Substituted Benzoquinones and Quinones via C-C Bond Formation
title_full A TfOH Catalyzed One-pot Synthesis of Aryl-Substituted Benzoquinones and Quinones via C-C Bond Formation
title_fullStr A TfOH Catalyzed One-pot Synthesis of Aryl-Substituted Benzoquinones and Quinones via C-C Bond Formation
title_full_unstemmed A TfOH Catalyzed One-pot Synthesis of Aryl-Substituted Benzoquinones and Quinones via C-C Bond Formation
title_sort tfoh catalyzed one-pot synthesis of aryl-substituted benzoquinones and quinones via c-c bond formation
publishDate 2015
url http://ndltd.ncl.edu.tw/handle/13452699380160562759
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