C6 picoloyl protection: a remote stereodirecting group for 2-deoxy-beta-glycoside formation
| dc.citation.epage | 5397 | en_US |
| dc.citation.issue | 25 | en_US |
| dc.citation.spage | 5394 | en_US |
| dc.citation.volume | 51 | en_US |
| dc.citation.woscount | 1 | en_US |
| dc.contributor.author | Ruei, Jyh-Herng | en_US |
| dc.contributor.author | Venukumar, Patteti | en_US |
| dc.contributor.author | Ingle, Arun B. | 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 | 2015-07-21T08:28:25Z | |
| dc.date.available | 2015-07-21T08:28:25Z | |
| dc.date.issued | 2015-01-01 | en_US |
| dc.description.abstract | We reported a remote control glycosylation method using the picoloyl protecting group for 2-deoxy-beta-glycosidic bond formation. The method is applicable to various 2-deoxythioglycosyl donors and the utility is illustrated by the synthesis of a deoxytrisaccharide component of landomycins. | en_US |
| dc.identifier.doi | 10.1039/c4cc08465a | en_US |
| dc.identifier.issn | 1359-7345 | en_US |
| dc.identifier.journal | CHEMICAL COMMUNICATIONS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1039/c4cc08465a | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/124591 | |
| dc.identifier.wosnumber | WOS:000351393600047 | en_US |
| dc.language.iso | en_US | en_US |
| dc.title | C6 picoloyl protection: a remote stereodirecting group for 2-deoxy-beta-glycoside formation | en_US |
| dc.type | Article | en_US |
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