Publication: Pyridine stabilized oxiranyl remote anions
| dc.contributor.author | Pattama Saisaha | en_US |
| dc.contributor.author | Chakkrapan Nerungsi | en_US |
| dc.contributor.author | Supitchaya Iamsaard | en_US |
| dc.contributor.author | Tienthong Thongpanchang | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.contributor.other | Thailand National Center for Genetic Engineering and Biotechnology | en_US |
| dc.date.accessioned | 2018-09-13T06:23:12Z | |
| dc.date.available | 2018-09-13T06:23:12Z | |
| dc.date.issued | 2009-07-22 | en_US |
| dc.description.abstract | The chemistry of oxiranyl remote anions derived from α,β-epoxypyridines is investigated. Deprotonation of α,β-epoxy pyridines at the β-position and reactions of the corresponding anions with a variety of electrophiles are found to be highly regioselective, possibly as a consequence of stabilization from the chelation between lithium and the pyridine moiety in the form of a five-membered cyclic intermediate. © 2009 Elsevier Ltd. All rights reserved. | en_US |
| dc.identifier.citation | Tetrahedron Letters. Vol.50, No.29 (2009), 4217-4220 | en_US |
| dc.identifier.doi | 10.1016/j.tetlet.2009.04.106 | en_US |
| dc.identifier.issn | 00404039 | en_US |
| dc.identifier.other | 2-s2.0-66549098790 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/27176 | |
| 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=66549098790&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 | Pyridine stabilized oxiranyl remote anions | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=66549098790&origin=inward | en_US |