Publication: Lanthanide triflate catalyzed generation of N-acyliminium ions from α-amido sulfones: the synthesis of (1-alkyl-1-aryl)methyl phenyl sulfones
dc.contributor.author | Chutima Kuhakarn | en_US |
dc.contributor.author | Kassrin Tangdenpaisal | en_US |
dc.contributor.author | Palangpon Kongsaeree | en_US |
dc.contributor.author | Samran Prabpai | en_US |
dc.contributor.author | Patoomratana Tuchinda | en_US |
dc.contributor.author | Manat Pohmakotr | en_US |
dc.contributor.author | Vichai Reutrakul | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-08-24T01:42:26Z | |
dc.date.available | 2018-08-24T01:42:26Z | |
dc.date.issued | 2007-04-02 | en_US |
dc.description.abstract | The reaction of α-amido sulfones with various aromatic and heteroaromatic compounds in the presence of a catalytic amount of lanthanide triflate provides a facile route for the synthesis of (1-alkyl-1-aryl)methyl phenyl sulfones. © 2007 Elsevier Ltd. All rights reserved. | en_US |
dc.identifier.citation | Tetrahedron Letters. Vol.48, No.14 (2007), 2467-2470 | en_US |
dc.identifier.doi | 10.1016/j.tetlet.2007.02.035 | en_US |
dc.identifier.issn | 00404039 | en_US |
dc.identifier.other | 2-s2.0-33847673216 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/24213 | |
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=33847673216&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 | Lanthanide triflate catalyzed generation of N-acyliminium ions from α-amido sulfones: the synthesis of (1-alkyl-1-aryl)methyl phenyl sulfones | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33847673216&origin=inward | en_US |