Optimization of asymmetric reduction conditions of 1-(benzo [d] [1,3] dioxol-5-yl) ethanone by Lactobacillus fermentum P1 using D-optimal experimental design-based model-Reference-Cited by-同舟云学术

Optimization of asymmetric reduction conditions of 1-(benzo [d] [1,3] dioxol-5-yl) ethanone by Lactobacillus fermentum P1 using D-optimal experimental design-based model

Published:2021-05-24 Issue:2 Volume:52 Page:218-225
ISSN:1082-6068
Container-title:Preparative Biochemistry & Biotechnology
language:en
Short-container-title:Preparative Biochemistry & Biotechnology

Author:

Özdemir Akın¹,Dertli Enes²,Şahin Engin³

Affiliation:

1. Faculty of Engineering, Industrial Engineering Department, Ondokuz Mayıs University, Samsun, Turkey

2. Chemical and Metallurgical Engineering Faculty, Food Engineering Department, Yildiz Technical University, Yildiz, Istanbul

3. Faculty of Health Sciences, Department of Nutrition and Dietetics, Bayburt University, Bayburt, Turkey

Publisher

Informa UK Limited

Subject

General Medicine,Biochemistry,Biotechnology

Link

https://www.tandfonline.com/doi/pdf/10.1080/10826068.2021.1925913

Reference27 articles.

1. Enantioselective resolution of racemic ibuprofen esters using different lipases immobilized on epoxy-functionalized silica

2. Enzymatic reductions for the chemist

3. New opportunities for biocatalysis: driving the synthesis of chiral chemicals

4. Lipase catalyzed synthesis of cinnamyl acetate via transesterification in non-aqueous medium

5. Ureas and thioureas as Rh-ligands for the enantioselective hydride transfer reduction of acetophenone

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