Photo-induced glycosylation using reusable organophotoacidsElectronic supplementary information (ESI) available. See DOI: 10.1039/c4cc04753b
The glycosylation reactions of glycosyl trichloroacetimidates and several alcohols using an organophotoacid as an activator under photoirradiation proceeded smoothly to give the corresponding glycosides in high yields. The organophotoacid was recovered and reused without any loss of efficiency. The...
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creator | Iwata, Ryosuke Uda, Kanjiro Takahashi, Daisuke Toshima, Kazunobu |
description | The glycosylation reactions of glycosyl trichloroacetimidates and several alcohols using an organophotoacid as an activator under photoirradiation proceeded smoothly to give the corresponding glycosides in high yields. The organophotoacid was recovered and reused without any loss of efficiency.
The glycosylation reactions of glycosyl trichloroacetimidates and several alcohols using an organophotoacid as an activator under photoirradiation proceeded smoothly to give the corresponding glycosides in high yields. |
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The glycosylation reactions of glycosyl trichloroacetimidates and several alcohols using an organophotoacid as an activator under photoirradiation proceeded smoothly to give the corresponding glycosides in high yields.</description><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFjsFKw0AQhpeiYK29eBfGmx5SE3bXtl41Yk8K9dBb2E4m6cpmd9lNhLyDD90GBQ9CncsMfP98_IxdZuksS_nyDgViKuaSb0dsnPF7kUix2JwMt1wmcy7kGTuP8SM9TCYXY_b1tnOtS7QtO6QSatOji71RrXYWuqhtDYG6qLaGwIVaWeeHB4W6jLkhbIOzGiF23htqyLYq9KBt5ULz7bjJ16tbUJ9Km0EygzURPL2uHuBv5wt2WikTafqzJ-zqOX9_fElCxMIH3RzkxW-c_8-vj_HClxXfAxbxYJw</recordid><startdate>20140814</startdate><enddate>20140814</enddate><creator>Iwata, Ryosuke</creator><creator>Uda, Kanjiro</creator><creator>Takahashi, Daisuke</creator><creator>Toshima, Kazunobu</creator><scope/></search><sort><creationdate>20140814</creationdate><title>Photo-induced glycosylation using reusable organophotoacidsElectronic supplementary information (ESI) available. See DOI: 10.1039/c4cc04753b</title><author>Iwata, Ryosuke ; Uda, Kanjiro ; Takahashi, Daisuke ; Toshima, Kazunobu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c4cc04753b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iwata, Ryosuke</creatorcontrib><creatorcontrib>Uda, Kanjiro</creatorcontrib><creatorcontrib>Takahashi, Daisuke</creatorcontrib><creatorcontrib>Toshima, Kazunobu</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iwata, Ryosuke</au><au>Uda, Kanjiro</au><au>Takahashi, Daisuke</au><au>Toshima, Kazunobu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photo-induced glycosylation using reusable organophotoacidsElectronic supplementary information (ESI) available. See DOI: 10.1039/c4cc04753b</atitle><date>2014-08-14</date><risdate>2014</risdate><volume>5</volume><issue>73</issue><spage>1695</spage><epage>1698</epage><pages>1695-1698</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>The glycosylation reactions of glycosyl trichloroacetimidates and several alcohols using an organophotoacid as an activator under photoirradiation proceeded smoothly to give the corresponding glycosides in high yields. The organophotoacid was recovered and reused without any loss of efficiency.
The glycosylation reactions of glycosyl trichloroacetimidates and several alcohols using an organophotoacid as an activator under photoirradiation proceeded smoothly to give the corresponding glycosides in high yields.</abstract><doi>10.1039/c4cc04753b</doi><tpages>4</tpages></addata></record> |
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title | Photo-induced glycosylation using reusable organophotoacidsElectronic supplementary information (ESI) available. See DOI: 10.1039/c4cc04753b |
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