Publication: 1,2-Cyclic sulfamidates as versatile precursors to thiomorpholines and piperazines
| dc.contributor.author | Andrew J. Williams | en_US |
| dc.contributor.author | Suda Chakthong | en_US |
| dc.contributor.author | Diane Gray | en_US |
| dc.contributor.author | Ron M. Lawrence | en_US |
| dc.contributor.author | Timothy Gallagher | en_US |
| dc.contributor.other | University of Bristol | en_US |
| dc.contributor.other | GlaxoSmithKline plc, United Kingdom | en_US |
| dc.contributor.other | Chulabhorn Research Institute | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-07-24T03:20:36Z | |
| dc.date.available | 2018-07-24T03:20:36Z | |
| dc.date.issued | 2003-03-20 | en_US |
| dc.description.abstract | (Matrix presented) 1,2-Cyclic sulfamidates undergo regiospecific nucleophilic displacement with either methyl thioglycolate or α-amino esters, followed by lactamization (thermal, base-mediated, or cyanide-catalyzed), to give thiomorpholin-3-ones and piperazin-2-ones. | en_US |
| dc.identifier.citation | Organic Letters. Vol.5, No.6 (2003), 811-814 | en_US |
| dc.identifier.doi | 10.1021/ol027418h | en_US |
| dc.identifier.issn | 15237060 | en_US |
| dc.identifier.other | 2-s2.0-0141627559 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/20754 | |
| 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=0141627559&origin=inward | en_US |
| dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | 1,2-Cyclic sulfamidates as versatile precursors to thiomorpholines and piperazines | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0141627559&origin=inward | en_US |