Publication: Synthesis of 2-(2-arylethyl)imidazoles by direct alkylation of 1-(n,n-dimethylaminomethyl)2-lithiomethylimidazole
dc.contributor.author | Bongkoch Tarnchompoo | en_US |
dc.contributor.author | Chachanat Thebtaranonth | en_US |
dc.contributor.author | Yodhathai Thebtaranonth | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-06-14T09:20:19Z | |
dc.date.available | 2018-06-14T09:20:19Z | |
dc.date.issued | 1990-01-01 | en_US |
dc.description.abstract | Direct deprotonation of 1-(N,N-dimethylaminomethyl)2-methylimidazole 4 by n-butyllithium yields anion 5 which can readily undergo alkylation reactions. This finding provides immediate access to 2-(2-arylethyl)imidazoles, 1, which are clumsy to prepare by other methods. © 1990. | en_US |
dc.identifier.citation | Tetrahedron Letters. Vol.31, No.40 (1990), 5779-5780 | en_US |
dc.identifier.doi | 10.1016/S0040-4039(00)97957-7 | en_US |
dc.identifier.issn | 00404039 | en_US |
dc.identifier.other | 2-s2.0-0025163548 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/15920 | |
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=0025163548&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 | Synthesis of 2-(2-arylethyl)imidazoles by direct alkylation of 1-(n,n-dimethylaminomethyl)2-lithiomethylimidazole | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0025163548&origin=inward | en_US |