Reducing disaccharides and their 1,2-dicarbonyl intermediates as building blocks for nitrogen heterocycles

被引:8
作者
Brust, Andreas [1 ,2 ]
Cuny, Eckehard [2 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
[2] Tech Univ Darmstadt, Clemens Schopf Inst Organ Chem & Biochem, D-97321 Darmstadt, Germany
关键词
HYDROPHILICALLY FUNCTIONALIZED PYRAZOLES; PYRANOSE; 2-OXIDASE; DICARBONYL SUGARS; RAW-MATERIALS; CHEMICAL-INDUSTRY; D-GLUCOSE; DERIVATIVES; CONVERSION; QUINOXALINE; ANNOUNCEMENT;
D O I
10.1039/c3ra47349j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The existential importance of a sustainable economy necessitates the utilisation of plant based renewable resources such as lignin and carbohydrates. Carbohydrate utilization as industrial raw materials requires low environmental impact conversions from sugars to high value products. Here we present the conversion of reducing disaccharides into industrially relevant heterocycles of the quinoxaline-, 1,2,4-triazine-, pyrazine-and pyrazolo[3,4-b]quinoxaline-type. Heterocycle formation was facilitated by chemical conversion of reducing sugars into 1,2-dicarbonyl intermediates and their subsequent cyclization with nitrogen bis-nucleophiles. A range of disaccharides was converted into quinoxalines carrying a diverse glycosylation pattern on the polyhydroxy alkyl side chain. All transformations were performed without the need of protecting group chemistry.
引用
收藏
页码:5759 / 5767
页数:9
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