Chemical Transformations of Biomass-Derived C6-Furanic Platform Chemicals for Sustainable Energy Research, Materials Science, and Synthetic Building Blocks

被引:240
|
作者
Kucherov, Fedor A. [1 ]
Romashov, Leonid V. [1 ]
Galkin, Konstantin I. [1 ]
Ananikov, Valentine P. [1 ]
机构
[1] Russian Acad Sci, Zelinsky Inst Organ Chem, Leninsky Pr 47, Moscow 119991, Russia
来源
基金
俄罗斯科学基金会;
关键词
Biomass processing; Platform chemicals; HMF; BHMF; DFF; FDCA; Sustainable development; Organic synthesis; SELECTIVE AEROBIC OXIDATION; CATALYTIC TRANSFER HYDROGENATION; GLASS-TRANSITION TEMPERATURE; COMPRESSED CARBON-DIOXIDE; METAL-ORGANIC FRAMEWORKS; PD ALLOY NANOPARTICLES; BASE-FREE CONDITIONS; ONE-POT CONVERSION; 2,5-FURANDICARBOXYLIC ACID; MILD CONDITIONS;
D O I
10.1021/acssuschemeng.8b00971
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recent advances in the area of biomass-derived C6-furanic platform chemicals for sustainable biomass processing are analyzed focusing on chemical reactions important for development of practical applications and materials science. Among the chemical processes currently being studied, tuning the amount of oxygen-containing functional groups remains the most active research direction. Production of efficient fuels requires the removal of oxygen atoms (reduction reactions), whereas utilization of biomass derived furanic derivatives in material science points out the transformation importance of oxidation in order to form dicarboxylic derivatives. Stimulated by this driving force, oxidation and reduction of 5-(hydroxymethyl)furfural (HMF) are nowadays massively studied. Moreover, these fundamental transformations are often used as model reactions to test new catalysts, and HMF transformations guide the development of new catalytic systems. From the viewpoint of organic synthesis, highly diverse chemical reactivity is explored and a number of bioderived synthetic building blocks with different functional groups are now accessible. This Perspective covers the most recent literature (since Jan 2017) to highlight the emerging research trends.
引用
收藏
页码:8064 / 8092
页数:57
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