Probing the Lewis Acid Catalyzed Acyclic Pathway of Carbohydrate Conversion in Methanol by In Situ NMR

التفاصيل البيبلوغرافية
العنوان: Probing the Lewis Acid Catalyzed Acyclic Pathway of Carbohydrate Conversion in Methanol by In Situ NMR
المؤلفون: Esben Taarning, Sebastian Meier, Pernille Rose Jensen
المصدر: Jensen, P R, Taarning, E & Meier, S 2019, ' Probing the Lewis Acid Catalyzed Acyclic Pathway of Carbohydrate Conversion in Methanol by In Situ NMR ', ChemCatChem, vol. 11, no. 20, pp. 5077-5084 . https://doi.org/10.1002/cctc.201901241
بيانات النشر: Wiley, 2019.
سنة النشر: 2019
مصطلحات موضوعية: In situ, Chemistry, Reaction pathway, Organic Chemistry, Kinetics, Biomass, Carbohydrate, Lewis acid, NMR, Catalysis, Inorganic Chemistry, chemistry.chemical_compound, Organic chemistry, Methanol, Lewis acids and bases, Physical and Theoretical Chemistry
الوصف: Future bioindustries will rely on the formation of diverse chemicals at high yield through various reaction pathways. These pathways include reactions to a series of alpha-hydroxy esters and acids that can be formed from the conversion of C3-C6 carbohydrates by Lewis acidic catalysts in alcohols and water. Definitive kinetic and mechanistic insights to support the development of carbohydrateconversion processes are arguably less developed than for analogous biocatalytic processes. Here, we visualize acyclic pathways of carbohydrate dehydration, using the acyclic C4 carbohydrate erythrulose as a probe molecule for the conversion by homogeneous SnCl4 in methanol. In situ studies allow the detection of previously postulated intermediates, identify the branch point to competing products and provide energetic and mechanistic insight by kineticanalysis. Reversibility of reactions, stereoselectivity and differential propensity for deuterium incorporation in competing pathways can be tracked by the formation of compounds with asymmetric mass distribution.
وصف الملف: application/pdf
تدمد: 1867-3899
1867-3880
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed885e1c591bfdacde6ae9993fc42801
https://doi.org/10.1002/cctc.201901241
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....ed885e1c591bfdacde6ae9993fc42801
قاعدة البيانات: OpenAIRE