Markedly improving asymmetric oxidation of 1-(4-methoxyphenyl) ethanol with Acetobacter sp. CCTCC M209061 cells by adding deep eutectic solvent in a two-phase system-Reference-Cited by-同舟云学术

Markedly improving asymmetric oxidation of 1-(4-methoxyphenyl) ethanol with Acetobacter sp. CCTCC M209061 cells by adding deep eutectic solvent in a two-phase system

Published:2016-01-13 Issue:1 Volume:15 Page:
ISSN:1475-2859
Container-title:Microbial Cell Factories
language:en
Short-container-title:Microb Cell Fact

Author:

Wei Ping,Liang Jing,Cheng Jing,Zong Min-Hua,Lou Wen-Yong

Funder

Program of State Key Laboratory of Pulp and Paper Engineering

National Natural Science Foundation of China (CN)

Key Program of Guangdong Natural Science Foundation

Fundamental Research Funds for the Chinese Universities

Open Funding Project of the State Key Laboratory of Bioreactor Engineering

Publisher

Springer Science and Business Media LLC

Subject

Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Link

http://link.springer.com/content/pdf/10.1186/s12934-015-0407-1

Reference50 articles.

1. Zilbeyaz K, Kurbanoglu EB. Production of (R)-1-(4-bromo-phenyl)-ethanol by locally isolated Aspergillus niger using ram horn peptone. Bioresour Technol. 2008;99:1549–52.

2. Goldberg K, Schroer K, Lutz S, Liese A. Biocatalytic ketone reduction—a powerful tool for the production of chiral alcohols—part II: whole-cell reductions. Appl Microbiol Biot. 2007;76:249–55.

3. Hillier MC, Marcoux JF, Zhao DL, Grabowski EJJ, McKeown AE, Tillyer RD. Stereoselective formation of carbon-carbon bonds via S(N)2-displacement: synthesis of substituted cycloalkyl b indoles. J Org Chem. 2005;70:8385–94.

4. Hillier MC, Desrosiers JN, Marcoux JF, Grabowski EJJ. Stereoselective carbon-carbon bond formation via the mitsunobu displacement of chiral secondary benzylic alcohols. Org Lett. 2004;6:573–6.

5. Lou WY, Wang W, Smith TJ, Zong M-H. Biocatalytic anti-Prelog stereoselective reduction of 4′-methoxyacetophenone to (R)-1-(4-methoxyphenyl)ethanol with immobilized Trigonopsis variabilis AS2.1611 cells using an ionic liquid-containing medium. Green Chem. 2009;11:1377–84.

Cited by 33 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Bioconversion of ricinoleic acid to (R)-γ-decalactone by Clavispora lusitaniae YJ26 cells in an ionic liquid–containing biphasic fermentation system;Food Bioscience;2024-10

2. An alkali substrate feeding engineering conversion platform for hesperetin 7‐O‐glucoside biosynthesis;International Journal of Food Science & Technology;2024-05-17

3. Biocatalysis for the Synthesis of Active Pharmaceutical Ingredients in Deep Eutectic Solvents: State-of-the-Art and Prospects;Catalysts;2024-01-19

4. Asymmetric biocatalysis in nonconventional media: neat conditions, eutectic solvents, and supercritical conditions;Biocatalysis in Asymmetric Synthesis;2024

5. Asymmetric Reduction of Cyclic Imines by Imine Reductase Enzymes in Non‐Conventional Solvents;ChemSusChem;2023-11-15