scholarly journals Simultaneous production of 5-hydroxymethylfurfural and furfural from bamboo (Phyllostachys nigra “Boryana”) in a biphasic reaction system

2020 ◽  
Vol 386 ◽  
pp. 123957 ◽  
Author(s):  
Nick Sweygers ◽  
Delphine E.C. Depuydt ◽  
Aart Willem Van Vuure ◽  
Jan Degrève ◽  
Geert Potters ◽  
...  
2017 ◽  
Vol 5 (7) ◽  
pp. 5694-5701 ◽  
Author(s):  
Ashutosh Mittal ◽  
Stuart K. Black ◽  
Todd B. Vinzant ◽  
Marykate O’Brien ◽  
Melvin P. Tucker ◽  
...  

ACS Catalysis ◽  
2014 ◽  
Vol 4 (11) ◽  
pp. 4021-4026 ◽  
Author(s):  
Samantha K. Au ◽  
Bettina R. Bommarius ◽  
Andreas S. Bommarius

RSC Advances ◽  
2016 ◽  
Vol 6 (32) ◽  
pp. 27004-27007 ◽  
Author(s):  
Miao Zuo ◽  
Zheng Li ◽  
Yetao Jiang ◽  
Xing Tang ◽  
Xianhai Zeng ◽  
...  

5-Chloromethylfurfural (5-CMF) was effectively prepared from fructose and other carbohydrates in a biphasic reaction system, which was composed of methyl isobutyl ketone (MIBK) and deep eutectic solvent (DES) with catalyst of AlCl3·6H2O.


2012 ◽  
Vol 135 (2) ◽  
pp. 373-379 ◽  
Author(s):  
Shuang Song ◽  
Ling-Zhi Cheong ◽  
Zheng Guo ◽  
Kasper Kristensen ◽  
Marianne Glasius ◽  
...  

2015 ◽  
Vol 81 (6) ◽  
pp. 1919-1925 ◽  
Author(s):  
Hiroshi Toda ◽  
Takuya Ohuchi ◽  
Ryouta Imae ◽  
Nobuya Itoh

ABSTRACTWe describe the development of biocatalysis for producing optically pure straight-chain (S)-epoxyalkanes using styrene monooxygenase ofRhodococcussp. strain ST-10 (RhSMO). RhSMO was expressed in the organic solvent-tolerant microorganismKocuria rhizophilaDC2201, and the bioconversion reaction was performed in an organic solvent-water biphasic reaction system. The biocatalytic process enantioselectively converted linear terminal alkenes to their corresponding (S)-epoxyalkanes using glucose and molecular oxygen. When 1-heptene and 6-chloro-1-hexene were used as substrates (400 mM) under optimized conditions, 88.3 mM (S)-1,2-epoxyheptane and 246.5 mM (S)-1,2-epoxy-6-chlorohexane, respectively, accumulated in the organic phase with good enantiomeric excess (ee; 84.2 and 95.5%). The biocatalysis showed broad substrate specificity toward various aliphatic alkenes, including functionalized and unfunctionalized alkenes, with good to excellent ee. Here, we demonstrate that this biocatalytic system is environmentally friendly and useful for producing various enantiopure (S)-epoxyalkanes.


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