<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen JS</submitter><funding>Ministry of Science and Technology, Taiwan</funding><funding>National Chung-Hsing University</funding><pagination>33853-33862</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9073715</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(58)</volume><pubmed_abstract>This work demonstrates the utilization of phosphotungstic acid (PTA) as a novel acidic catalyst for carbohydrate reactions, such as per-&lt;i>O&lt;/i>-acetylation, regioselective &lt;i>O&lt;/i>-4,6 benzylidene acetal formation, regioselective &lt;i>O&lt;/i>-4 ring-opening, and glycosylation. These reactions are basic and salient during the synthesis of carbohydrate-based bioactive oligomers. Phosphotungstic acid's high acidity and eco-friendly character make it a tempting alternative to corrosive homogeneous acids. The various homogenous acid catalysts were replaced by the phosphotungstic acid solely for different carbohydrate reactions. It can be widely used as a catalyst for organic reactions as it is thermally stable and easy to handle. In our work, the reactions are operated smoothly under ambient condi</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Phosphotungstic acid as a novel acidic catalyst for carbohydrate protection and glycosylation.</pubmed_title><pmcid>PMC9073715</pmcid><funding_grant_id>MOST 107-2113-M-005-021</funding_grant_id><pubmed_authors>Chen JS</pubmed_authors><pubmed_authors>Wu HR</pubmed_authors><pubmed_authors>Luo SY</pubmed_authors><pubmed_authors>Sankar A</pubmed_authors><pubmed_authors>Lin YJ</pubmed_authors><pubmed_authors>Huang PH</pubmed_authors><pubmed_authors>Liao CH</pubmed_authors><pubmed_authors>Wu SS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phosphotungstic acid as a novel acidic catalyst for carbohydrate protection and glycosylation.</name><description>This work demonstrates the utilization of phosphotungstic acid (PTA) as a novel acidic catalyst for carbohydrate reactions, such as per-&lt;i>O&lt;/i>-acetylation, regioselective &lt;i>O&lt;/i>-4,6 benzylidene acetal formation, regioselective &lt;i>O&lt;/i>-4 ring-opening, and glycosylation. These reactions are basic and salient during the synthesis of carbohydrate-based bioactive oligomers. Phosphotungstic acid's high acidity and eco-friendly character make it a tempting alternative to corrosive homogeneous acids. The various homogenous acid catalysts were replaced by the phosphotungstic acid solely for different carbohydrate reactions. It can be widely used as a catalyst for organic reactions as it is thermally stable and easy to handle. In our work, the reactions are operated smoothly under ambient condi</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Oct</publication><modification>2025-04-26T15:16:53.086Z</modification><creation>2025-04-06T14:53:08.024Z</creation></dates><accession>S-EPMC9073715</accession><cross_references><pubmed>35528919</pubmed><doi>10.1039/c9ra06170c</doi></cross_references></HashMap>