Desymmetrization of 2,4,5,6-Tetra-O-benzyl-D-myo-inositol for the Synthesis of Mycothiol
| dc.citation.epage | 5499 | en_US |
| dc.citation.issue | 20 | en_US |
| dc.citation.spage | 5496 | en_US |
| dc.citation.volume | 13 | en_US |
| dc.citation.woscount | 5 | |
| dc.contributor.author | Chung, Chuan-Chung | en_US |
| dc.contributor.author | Zulueta, Medel Manuel L. | en_US |
| dc.contributor.author | Padiyar, Laxmansingh T. | en_US |
| dc.contributor.author | Hung, Shang-Cheng | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:20:42Z | |
| dc.date.available | 2014-12-08T15:20:42Z | |
| dc.date.issued | 2011-10-21 | en_US |
| dc.description.abstract | An efficient chemical synthesis of mycothiol Involving the regioselective ketopinyl desymmetrization of 2,4,5,6-tetrabenzylated D-myo-inositol as the key step Is described. Together with a highly alpha-stereoselective D-glucosaminylation, the whole procedure was accomplished in eight steps with an overall yield of 40%. | en_US |
| dc.identifier.doi | 10.1021/ol202218n | en_US |
| dc.identifier.issn | 1523-7060 | en_US |
| dc.identifier.journal | ORGANIC LETTERS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1021/ol202218n | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/14727 | |
| dc.identifier.wosnumber | WOS:000295817100022 | |
| dc.language.iso | en_US | en_US |
| dc.title | Desymmetrization of 2,4,5,6-Tetra-O-benzyl-D-myo-inositol for the Synthesis of Mycothiol | en_US |
| dc.type | Article | en_US |