<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>21(18)</volume><submitter>Plata E</submitter><pubmed_abstract>To exploit the hydrolytic activity and high selectivity of immobilized lipase B from Candida antarctica on octyl agarose (CALB-OC) in the hydrolysis of triacetin and also to produce new value-added compounds from glycerol, this work describes a chemoenzymatic methodology for the synthesis of the new dimeric glycerol ester 3-((2,3-diacetoxypropanoyl)oxy)propane-1,2-diyl diacetate. According to this approach, triacetin was regioselectively hydrolyzed to 1,2-diacetin with CALB-OC. The diglyceride product was subsequently oxidized with pyridinium chlorochromate (PCC) and a dimeric ester was isolated as the only product. It was found that the medium acidity during the PCC treatment and a high 1,2-diacetin concentration favored the formation of the ester. The synthesized compounds were character</pubmed_abstract><journal>International journal of molecular sciences</journal><pagination>6501</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7555366</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Chemoenzymatic Synthesis of the New 3-((2,3-Diacetoxypropanoyl)oxy)propane-1,2-diyl Diacetate Using Immobilized Lipase B from Candidaantarctica and Pyridinium Chlorochromate as an Oxidizing Agent.</pubmed_title><pmcid>PMC7555366</pmcid><pubmed_authors>Ruiz J</pubmed_authors><pubmed_authors>Castillo JJ</pubmed_authors><pubmed_authors>Fernandez-Lafuente R</pubmed_authors><pubmed_authors>Plata E</pubmed_authors><pubmed_authors>Ortiz C</pubmed_authors><pubmed_authors>Ruiz M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chemoenzymatic Synthesis of the New 3-((2,3-Diacetoxypropanoyl)oxy)propane-1,2-diyl Diacetate Using Immobilized Lipase B from Candidaantarctica and Pyridinium Chlorochromate as an Oxidizing Agent.</name><description>To exploit the hydrolytic activity and high selectivity of immobilized lipase B from Candida antarctica on octyl agarose (CALB-OC) in the hydrolysis of triacetin and also to produce new value-added compounds from glycerol, this work describes a chemoenzymatic methodology for the synthesis of the new dimeric glycerol ester 3-((2,3-diacetoxypropanoyl)oxy)propane-1,2-diyl diacetate. According to this approach, triacetin was regioselectively hydrolyzed to 1,2-diacetin with CALB-OC. The diglyceride product was subsequently oxidized with pyridinium chlorochromate (PCC) and a dimeric ester was isolated as the only product. It was found that the medium acidity during the PCC treatment and a high 1,2-diacetin concentration favored the formation of the ester. The synthesized compounds were character</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Sep</publication><modification>2025-05-29T19:38:30.876Z</modification><creation>2025-05-29T19:38:30.876Z</creation></dates><accession>S-EPMC7555366</accession><cross_references><pubmed>32899537</pubmed><doi>10.3390/ijms21186501</doi></cross_references></HashMap>