Reactivity of chlorinating agents/PPh<inf>3</inf>for the chlorination of alcohols and carboxylic acids: a comparative study
The reactivity of chlorinating agents was examined with the aid of1H NMR using competitive reactions between selected chlorinating agents and CBr4towards alcohols and carboxylic acids. The reactivity was greatly dependent on the type of substituent on the chlorinating agents. COCCl3and CN substitute...
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th-mahidol.242672018-08-24T09:16:05Z Reactivity of chlorinating agents/PPh<inf>3</inf>for the chlorination of alcohols and carboxylic acids: a comparative study Wanchai Pluempanupat Oraphin Chantarasriwong Piyada Taboonpong Doo Ok Jang Warinthorn Chavasiri Mahidol University Yonsei University Wonju Campus Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics The reactivity of chlorinating agents was examined with the aid of1H NMR using competitive reactions between selected chlorinating agents and CBr4towards alcohols and carboxylic acids. The reactivity was greatly dependent on the type of substituent on the chlorinating agents. COCCl3and CN substituted trichloromethyl groups enhanced the reactivity of the chlorinating agent with PPh3for the chlorination of alcohols and carboxylic acids. © 2006 Elsevier Ltd. All rights reserved. 2018-08-24T01:43:50Z 2018-08-24T01:43:50Z 2007-01-08 Article Tetrahedron Letters. Vol.48, No.2 (2007), 223-226 10.1016/j.tetlet.2006.11.060 00404039 2-s2.0-33845221264 https://repository.li.mahidol.ac.th/handle/123456789/24267 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33845221264&origin=inward |
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Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Wanchai Pluempanupat Oraphin Chantarasriwong Piyada Taboonpong Doo Ok Jang Warinthorn Chavasiri Reactivity of chlorinating agents/PPh<inf>3</inf>for the chlorination of alcohols and carboxylic acids: a comparative study |
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The reactivity of chlorinating agents was examined with the aid of1H NMR using competitive reactions between selected chlorinating agents and CBr4towards alcohols and carboxylic acids. The reactivity was greatly dependent on the type of substituent on the chlorinating agents. COCCl3and CN substituted trichloromethyl groups enhanced the reactivity of the chlorinating agent with PPh3for the chlorination of alcohols and carboxylic acids. © 2006 Elsevier Ltd. All rights reserved. |
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Mahidol University |
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Mahidol University Wanchai Pluempanupat Oraphin Chantarasriwong Piyada Taboonpong Doo Ok Jang Warinthorn Chavasiri |
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Article |
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Wanchai Pluempanupat Oraphin Chantarasriwong Piyada Taboonpong Doo Ok Jang Warinthorn Chavasiri |
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Wanchai Pluempanupat |
title |
Reactivity of chlorinating agents/PPh<inf>3</inf>for the chlorination of alcohols and carboxylic acids: a comparative study |
title_short |
Reactivity of chlorinating agents/PPh<inf>3</inf>for the chlorination of alcohols and carboxylic acids: a comparative study |
title_full |
Reactivity of chlorinating agents/PPh<inf>3</inf>for the chlorination of alcohols and carboxylic acids: a comparative study |
title_fullStr |
Reactivity of chlorinating agents/PPh<inf>3</inf>for the chlorination of alcohols and carboxylic acids: a comparative study |
title_full_unstemmed |
Reactivity of chlorinating agents/PPh<inf>3</inf>for the chlorination of alcohols and carboxylic acids: a comparative study |
title_sort |
reactivity of chlorinating agents/pph<inf>3</inf>for the chlorination of alcohols and carboxylic acids: a comparative study |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/24267 |
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1763496551340048384 |