Paper Infomation
Application of Biocatalysis in Fine Chemical Industry
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Author: Mingze Wu, Tianci Zhou, Xianan Gao
Abstract: The chemical industry has become one of the foundation of the national economy pillar industry, but at the same time, the environmental pollution problems caused by the chemical industry should not be ignored, so the sustainable development of chemical industry, constantly looking for new economic growing point, and the application of biocatalysis technology reform and gradually replace the traditional chemical products is one of the future development direction. Biocatalysis is characterized by mild conditions, energy saving, high conversion rate and selection rate, and environmental friendliness. It can also be used for the synthesis of chiral compounds and the synthesis of macromolecules and macromolecules with complex structures and biological activities.
Keywords: Biocatalysis, High Catalytic Efficiency, Specificity, Environment Friendly
References:
[1] Kawano S, Horikawa M, Yasohara Y, et al. Microbial enantioselective reduction of aeetylpyridine derivatiyes[J]. Biosci.Biotechnol.Biochem. 2003,67(4):809-815.
[2] Martines CA, Hu S, Dumond Y, et al., Development of a chemoenzymatic manufacturing process for process for pregabalin[J]. Organic Process Reseaarch&Development, 2008,12(3):392-398.
[3] Anna Brodzka, Dominik Koszelewski, Ryszard Ostaszewski. The studies on chemoenzymatic synthesis of Femoxetine [J]. Journal of Molecular Catalysis B: Enzymatic, 2012, 82:96-101.
[4] Xue-Dong Li, Lang Xiandong, Song Qingwen, Guo Yakun, He Liangnian. copper (Ⅰ) catalysis of atmospheric carbon dioxide, the three components of propargyl alcohol and secondary amine reaction [J]. 2016 (04) organic chemistry.
[5] Xia Xiaofeng, Li Lianhua, Liang Yongmin. Study on rearrangement of propargyl ester catalyzed by platinum and c-h functionalization of ortho-position of tertiary amine nitrogen atoms [J]. Organic chemistry. 2013(04)
[6] Jin Dekuan. Ionic liquid [Bmim] cl-crcl2 promotes the synthesis of high propargyl compounds [J]. Chemical world. 2011(07)
[7] Zhu Haitao, Luo Tingting, Tong Xiaojuan, Zhou Nini, Yang Desuo, Fan Mingjin, Zhao Lifang. Journal of baoji university of arts and sciences (natural science edition). 2018(01)
[8] Pei-Fang Liu, Chen Jian, Maike Zha. Unsaturated alcohol electric reduction of mass spectrometry, electrochemical cyclic voltammetric method (MSCV) research Ⅱ. Electric reduction of propargyl alcohol [J]. Journal of chemistry. 1993 (02)
[9] Xu Wenshuai, Zhao Shoujing, Luo Xiaopei, Song Jinna, Liu Jian-Quan, Bi Xihe, Liao Peiqiu. Silver catalyzed cross-coupling reaction of propargyl alcohol with aryl isonitrile: atomic economy synthesis of n-aryl -2, 3-bienolamide [J]. Organic chemistry. 2015(10)
[10] Chun-Mei Du, Han Lingli, Liu Tao, Zhang-Yu Yu. Pt (Ⅱ) catalytic high molecular mechanism of inner loop addition reaction of propargyl alcohol research [J]. Journal of jining college. 2012 (6)
[11] He Qiwen, Aso Ming. Synthesis of optically active propargyl alcohol [J]. Organic chemistry. 2002(06)