Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid

Mild and highly regioselective monoiodination of phenol and analogues is achieved in high to excellent yields at room temperature with a combination of stoichiometric p-toluenesulfonic acid and N-iodosuccinimide. © 2009 Elsevier Ltd. All rights reserved.

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Bibliographic Details
Main Authors:	Pakorn Bovonsombat, Juthamard Leykajarakul, Chiraphorn Khan, Kawin Pla-on, Michael M. Krause, Pratheep Khanthapura, Rameez Ali, Niran Doowa
Other Authors:	Mahidol University
Format:	Article
Published:	2018
Subjects:	Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics
Online Access:	https://repository.li.mahidol.ac.th/handle/123456789/27203
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Institution:	Mahidol University

id	th-mahidol.27203
record_format	dspace
spelling	th-mahidol.272032018-09-13T14:12:28Z Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid Pakorn Bovonsombat Juthamard Leykajarakul Chiraphorn Khan Kawin Pla-on Michael M. Krause Pratheep Khanthapura Rameez Ali Niran Doowa Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Mild and highly regioselective monoiodination of phenol and analogues is achieved in high to excellent yields at room temperature with a combination of stoichiometric p-toluenesulfonic acid and N-iodosuccinimide. © 2009 Elsevier Ltd. All rights reserved. 2018-09-13T06:24:00Z 2018-09-13T06:24:00Z 2009-06-03 Article Tetrahedron Letters. Vol.50, No.22 (2009), 2664-2667 10.1016/j.tetlet.2009.03.128 00404039 2-s2.0-64549113446 https://repository.li.mahidol.ac.th/handle/123456789/27203 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=64549113446&origin=inward
institution	Mahidol University
building	Mahidol University Library
continent	Asia
country	Thailand Thailand
content_provider	Mahidol University Library
collection	Mahidol University Institutional Repository
topic	Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics
spellingShingle	Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Pakorn Bovonsombat Juthamard Leykajarakul Chiraphorn Khan Kawin Pla-on Michael M. Krause Pratheep Khanthapura Rameez Ali Niran Doowa Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid
description	Mild and highly regioselective monoiodination of phenol and analogues is achieved in high to excellent yields at room temperature with a combination of stoichiometric p-toluenesulfonic acid and N-iodosuccinimide. © 2009 Elsevier Ltd. All rights reserved.
author2	Mahidol University
author_facet	Mahidol University Pakorn Bovonsombat Juthamard Leykajarakul Chiraphorn Khan Kawin Pla-on Michael M. Krause Pratheep Khanthapura Rameez Ali Niran Doowa
format	Article
author	Pakorn Bovonsombat Juthamard Leykajarakul Chiraphorn Khan Kawin Pla-on Michael M. Krause Pratheep Khanthapura Rameez Ali Niran Doowa
author_sort	Pakorn Bovonsombat
title	Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid
title_short	Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid
title_full	Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid
title_fullStr	Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid
title_full_unstemmed	Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid
title_sort	regioselective iodination of phenol and analogues using n-iodosuccinimide and p-toluenesulfonic acid
publishDate	2018
url	https://repository.li.mahidol.ac.th/handle/123456789/27203
_version_	1763497314573352960

Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid

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