Department of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, UK.
Department of Biochemical Engineering, University College London, Bernard Katz Building, London, WC1E 6BT, UK.
Angew Chem Int Ed Engl. 2019 Mar 18;58(12):3854-3858. doi: 10.1002/anie.201813712. Epub 2019 Feb 14.
Carbohydrates are the major component of biomass and have unique potential as a sustainable source of building blocks for chemicals, materials, and biofuels because of their low cost, ready availability, and stereochemical diversity. With a view to upgrading carbohydrates to access valuable nitrogen-containing sugar-like compounds such as aminopolyols, biocatalytic aminations using transaminase enzymes (TAms) have been investigated as a sustainable alternative to traditional synthetic strategies. Demonstrated here is the reaction of TAms with sugar-derived tetrahydrofuran (THF) aldehydes, obtained from the regioselective dehydration of biomass-derived sugars, to provide access to cyclic aminodiols in high yields. In a preliminary study we have also established the direct transamination of sugars to give acyclic aminopolyols. Notably, the reaction of the ketose d-fructose proceeds with complete stereoselectivity to yield valuable aminosugars in high purity.
碳水化合物是生物质的主要组成部分,由于其成本低、易得性和立体化学多样性,具有作为化学品、材料和生物燃料构建块的可持续来源的独特潜力。为了将碳水化合物升级为有价值的含氮糖类似物,如氨基多元醇,使用转氨酶(TAms)的生物催化胺化已被研究作为传统合成策略的可持续替代方案。本文展示了 TAms 与糖衍生的四氢呋喃(THF)醛的反应,这些醛是通过生物质衍生糖的区域选择性脱水获得的,可高收率得到环状氨基二醇。在初步研究中,我们还建立了糖的直接转氨反应,得到无环氨基多元醇。值得注意的是,酮糖 d-果糖的反应具有完全的立体选择性,以高纯度得到有价值的氨基糖。