Publication: Glycolaldehyde monomer in organic synthesis
| dc.contributor.author | P. Dinprasert | en_US |
| dc.contributor.author | C. Mahidol | en_US |
| dc.contributor.author | C. Thebtaranonth | en_US |
| dc.contributor.author | Y. Thebtaranonth | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-06-14T09:12:52Z | |
| dc.date.available | 2018-06-14T09:12:52Z | |
| dc.date.issued | 1989-01-01 | en_US |
| dc.description.abstract | The lithium alkoxide of glycolaldehyde can be generated and trapped in situ by keto- and ester enolates to yield the corresponding keto-epoxides and hydroxy lactones respectively. © 1989. | en_US |
| dc.identifier.citation | Tetrahedron Letters. Vol.30, No.9 (1989), 1149-1152 | en_US |
| dc.identifier.doi | 10.1016/S0040-4039(01)80384-1 | en_US |
| dc.identifier.issn | 00404039 | en_US |
| dc.identifier.other | 2-s2.0-0010397408 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/15715 | |
| 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=0010397408&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 | Glycolaldehyde monomer in organic synthesis | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0010397408&origin=inward | en_US |
