Formal Synthesis of 3-Deoxy-D-manno-Octulosonic Acid (KDO) and 3-Deoxy-D-arabino-2-heptulosonic Acid (DAH)
| dc.citation.epage | 222 | en_US |
| dc.citation.issue | 2 | en_US |
| dc.citation.spage | 219 | en_US |
| dc.citation.volume | en_US | |
| dc.citation.woscount | 2 | |
| dc.contributor.author | Pradhan, Tapan Kumar | en_US |
| dc.contributor.author | Lin, Chun Cheng | en_US |
| dc.contributor.author | Mong, Kwok Kong Tony | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:29:39Z | |
| dc.date.available | 2014-12-08T15:29:39Z | |
| dc.date.issued | 2013-01-01 | en_US |
| dc.description.abstract | Practical synthetic routes to 3-deoxy-D-manno-octulo-sonic acid (KDO) and 3-deoxy-D-arabino-2-heptulosonic acid (DAH) from common sugar substrates are reported. Chain homologation of the sugar substrates was accomplished by Wittig olefination and Corey-Fuchs alkynylation. A new cyclization strategy was investigated to access the desired pyranosyl isomer of the KDO target. | en_US |
| dc.identifier.doi | 10.1055/s-0032-1317932 | en_US |
| dc.identifier.issn | 0936-5214 | en_US |
| dc.identifier.journal | SYNLETT | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1055/s-0032-1317932 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/21295 | |
| dc.identifier.wosnumber | WOS:000314697700019 | |
| dc.language.iso | en_US | en_US |
| dc.subject | carbohydrates | en_US |
| dc.subject | Wittig | en_US |
| dc.subject | Corey-Fuchs | en_US |
| dc.subject | cyclization | en_US |
| dc.title | Formal Synthesis of 3-Deoxy-D-manno-Octulosonic Acid (KDO) and 3-Deoxy-D-arabino-2-heptulosonic Acid (DAH) | en_US |
| dc.type | Article | en_US |