Publication: Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid
dc.contributor.author | Pakorn Bovonsombat | en_US |
dc.contributor.author | Juthamard Leykajarakul | en_US |
dc.contributor.author | Chiraphorn Khan | en_US |
dc.contributor.author | Kawin Pla-on | en_US |
dc.contributor.author | Michael M. Krause | en_US |
dc.contributor.author | Pratheep Khanthapura | en_US |
dc.contributor.author | Rameez Ali | en_US |
dc.contributor.author | Niran Doowa | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-09-13T06:24:00Z | |
dc.date.available | 2018-09-13T06:24:00Z | |
dc.date.issued | 2009-06-03 | en_US |
dc.description.abstract | 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. | en_US |
dc.identifier.citation | Tetrahedron Letters. Vol.50, No.22 (2009), 2664-2667 | en_US |
dc.identifier.doi | 10.1016/j.tetlet.2009.03.128 | en_US |
dc.identifier.issn | 00404039 | en_US |
dc.identifier.other | 2-s2.0-64549113446 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/27203 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=64549113446&origin=inward | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=64549113446&origin=inward | en_US |