| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1388078 | Carbohydrate Research | 2013 | 5 Pages |
When treated with trichloroacetonitrile in the presence of 1,8-diazabicyclo[5,4,0]-undec-7-ene, the (2-nitrophenyl)acetyl protecting group (NPAc) was partially transformed into mono-(NPClAc) and dichlorinated (NPCl2Ac) species, but no chlorination occurred in the presence of solid potassium carbonate. The monochlorinated NPClAc group, which is suitable for use in glycosylation reaction, can be selectively removed by treatment with thiourea.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► The (2-nitrophenyl)acetyl (NPAc) protecting group was partially chlorinated in the presence of trichloroacetonitrile and DBU. ► The (2-nitrophenyl)chloroacetyl (NPClAc) group can be selectively removed by treatment with thiourea. ► The NPClAc group is suitable for use in glycosylation reaction.
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