<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang L</submitter><funding>China Scholarship Council</funding><funding>European Research Council</funding><pagination>1994-2003</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6470887</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2019(10)</volume><pubmed_abstract>Pre-activation based glycosylations have become a very powerful tool in the assembly of oligosaccharides and the use of nucleophilic additives allows for the in situ generation of reactive intermediates with tailored reactivity. We here use a glycosylation strategy that is based on the use of per-benzylated imidate building blocks for the fully stereoselective construction of a spacer equipped &lt;i>Aspergillus fumigatus&lt;/i> α-1,3-octaglucan. We have used the trimethylsilyl iodide (TMSI)-triphenylphosphine oxide (Ph&lt;sub>3&lt;/sub>P=O) for the stereoselective installation of an azidopropanol spacer and triflic acid (TfOH)-dimethyl formamide (DMF) enabled glycosylations for the coupling reactions with the secondary glucosyl C-3-alcohols. An operationally simple in situ activation coupling procedur</pubmed_abstract><journal>European journal of organic chemistry</journal><pubmed_title>Reagent Controlled Stereoselective Assembly of α-(1,3)-Glucans.</pubmed_title><pmcid>PMC6470887</pmcid><funding_grant_id>726072</funding_grant_id><pubmed_authors>Overkleeft HS</pubmed_authors><pubmed_authors>Codee JDC</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>van der Marel GA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Reagent Controlled Stereoselective Assembly of α-(1,3)-Glucans.</name><description>Pre-activation based glycosylations have become a very powerful tool in the assembly of oligosaccharides and the use of nucleophilic additives allows for the in situ generation of reactive intermediates with tailored reactivity. We here use a glycosylation strategy that is based on the use of per-benzylated imidate building blocks for the fully stereoselective construction of a spacer equipped &lt;i>Aspergillus fumigatus&lt;/i> α-1,3-octaglucan. We have used the trimethylsilyl iodide (TMSI)-triphenylphosphine oxide (Ph&lt;sub>3&lt;/sub>P=O) for the stereoselective installation of an azidopropanol spacer and triflic acid (TfOH)-dimethyl formamide (DMF) enabled glycosylations for the coupling reactions with the secondary glucosyl C-3-alcohols. An operationally simple in situ activation coupling procedur</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Mar</publication><modification>2025-04-26T23:07:22.156Z</modification><creation>2019-06-06T22:46:55Z</creation></dates><accession>S-EPMC6470887</accession><cross_references><pubmed>31007571</pubmed><doi>10.1002/ejoc.201800894</doi></cross_references></HashMap>