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Refinado por: assunto: Chiral Alcohols remover Base de dados/Biblioteca: DOAJ Directory of Open Access Journals remover
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Chemoenzymatic Synthesis of Optically Active Alcohols Possessing 1,2,3,4-Tetrahydroquinoline Moiety Employing Lipases or Variants of the Acyltransferase from Mycobacterium smegmatis
Chemoenzymatic Synthesis of Optically Active Alcohols Possessing 1,2,3,4-Tetrahydroquinoline Moiety Employing Lipases or Variants of the Acyltransferase from Mycobacterium smegmatis
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Chemoenzymatic Synthesis of Optically Active Alcohols Possessing 1,2,3,4-Tetrahydroquinoline Moiety Employing Lipases or Variants of the Acyltransferase from Mycobacterium smegmatis

Zdun, Beata ; Kopińska, Izabela ; Dranka, Maciej ; Reiter, Tamara ; Kroutil, Wolfgang ; Borowiecki, Paweł

Catalysts, 2022-12, Vol.12 (12), p.1610 [Periódico revisado por pares]

Basel: MDPI AG

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2
A Comparative Study on Asymmetric Reduction of Ketones Using the Growing and Resting Cells of Marine-Derived Fungi
A Comparative Study on Asymmetric Reduction of Ketones Using the Growing and Resting Cells of Marine-Derived Fungi
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A Comparative Study on Asymmetric Reduction of Ketones Using the Growing and Resting Cells of Marine-Derived Fungi

Liu, Hui ; Chen, Bi-Shuang ; de Souza, Fayene Zeferino Ribeiro ; Liu, Lan

Marine drugs, 2018-02, Vol.16 (2), p.62 [Periódico revisado por pares]

Switzerland: MDPI AG

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3
Ru-Catalyzed Asymmetric Addition of Arylboronic Acids to Aliphatic Aldehydes via P-Chiral Monophosphorous Ligands
Ru-Catalyzed Asymmetric Addition of Arylboronic Acids to Aliphatic Aldehydes via P-Chiral Monophosphorous Ligands
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Ru-Catalyzed Asymmetric Addition of Arylboronic Acids to Aliphatic Aldehydes via P-Chiral Monophosphorous Ligands

Miao, Rui ; Xia, Yanping ; Wei, Yifei ; Ouyang, Lu ; Luo, Renshi

Molecules (Basel, Switzerland), 2022-06, Vol.27 (12), p.3898 [Periódico revisado por pares]

Basel: MDPI AG

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4
New Anti-Prelog Stereospecific Whole-Cell Biocatalyst for Asymmetric Reduction of Prochiral Ketones
New Anti-Prelog Stereospecific Whole-Cell Biocatalyst for Asymmetric Reduction of Prochiral Ketones
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New Anti-Prelog Stereospecific Whole-Cell Biocatalyst for Asymmetric Reduction of Prochiral Ketones

Wang, Min-Yu ; Cai, Shun-Ju ; Lin, Jia-Chun ; Ji, Xiao-Jun ; Zhang, Zhi-Gang

Molecules (Basel, Switzerland), 2023-02, Vol.28 (3), p.1422 [Periódico revisado por pares]

Switzerland: MDPI AG

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5
Sterically controlled rhenium-catalyzed hydroxyl transposition
Sterically controlled rhenium-catalyzed hydroxyl transposition
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Sterically controlled rhenium-catalyzed hydroxyl transposition

Caron-Duval, Edouard ; Spino, Claude Royer, Jacques

ARKIVOC free online journal of organic chemistry, 2024-01, Vol.2024 (2) [Periódico revisado por pares]

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6
Tween® 20-Enhanced Bioreduction of Acetophenones Promoted by Daucus carota Root
Tween® 20-Enhanced Bioreduction of Acetophenones Promoted by Daucus carota Root
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Tween® 20-Enhanced Bioreduction of Acetophenones Promoted by Daucus carota Root

Monique Rodrigues da Costa ; Álvaro Takeo Omori

Food technology and biotechnology, 2017-01, Vol.55 (2), p.231-235 [Periódico revisado por pares]

University of Zagreb Faculty of Food Technology and Biotechnology

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7
Evolutionary coupling-inspired engineering of alcohol dehydrogenase reveals the influence of distant sites on its catalytic efficiency for stereospecific synthesis of chiral alcohols
Evolutionary coupling-inspired engineering of alcohol dehydrogenase reveals the influence of distant sites on its catalytic efficiency for stereospecific synthesis of chiral alcohols
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Evolutionary coupling-inspired engineering of alcohol dehydrogenase reveals the influence of distant sites on its catalytic efficiency for stereospecific synthesis of chiral alcohols

Gu, Jie ; Sim, Byu Ri ; Li, Jiarui ; Yu, Yangqing ; Qin, Lei ; Wu, Lunjie ; Shen, Yu ; Nie, Yao ; Zhao, Yi-Lei ; Xu, Yan

Computational and structural biotechnology journal, 2021-01, Vol.19, p.5864-5873 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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8
Efficient Biosynthesis of (S)-1-chloro-2-heptanol Catalyzed by a Newly Isolated Fungi Curvularia hominis B-36
Efficient Biosynthesis of (S)-1-chloro-2-heptanol Catalyzed by a Newly Isolated Fungi Curvularia hominis B-36
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Efficient Biosynthesis of (S)-1-chloro-2-heptanol Catalyzed by a Newly Isolated Fungi Curvularia hominis B-36

Xu, Shenpeng ; Lin, Qinzhe ; Chen, Wentian ; Lin, Ruoyu ; Shen, Yikai ; Tang, Pinchuan ; Yu, Sisi ; Du, Wenting ; Li, Jun

Catalysts, 2023-01, Vol.13 (1), p.52 [Periódico revisado por pares]

Basel: MDPI AG

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9
Increased availability of NADH in metabolically engineered baker's yeast improves transaminase-oxidoreductase coupled asymmetric whole-cell bioconversion
Increased availability of NADH in metabolically engineered baker's yeast improves transaminase-oxidoreductase coupled asymmetric whole-cell bioconversion
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Increased availability of NADH in metabolically engineered baker's yeast improves transaminase-oxidoreductase coupled asymmetric whole-cell bioconversion

Knudsen, Jan Dines ; Hägglöf, Cecilia ; Weber, Nora ; Carlquist, Magnus

Microbial cell factories, 2016-02, Vol.15 (31), p.37-37, Article 37 [Periódico revisado por pares]

England: BioMed Central Ltd

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10
Enzymatic characterization of a recombinant carbonyl reductase from Acetobacter sp. CCTCC M209061
Enzymatic characterization of a recombinant carbonyl reductase from Acetobacter sp. CCTCC M209061
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Enzymatic characterization of a recombinant carbonyl reductase from Acetobacter sp. CCTCC M209061

Wei, Ping ; Cui, Yu-Han ; Zong, Min-Hua ; Xu, Pei ; Zhou, Jian ; Lou, Wen-Yong

Bioresources and bioprocessing, 2017-01, Vol.4 (1), p.39-39, Article 39 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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