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Refinado por: assunto: Chiral Alcohols remover
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11
Highly Enantioselective Production of Chiral Secondary Alcohols Using Lactobacillus paracasei BD101 as a New Whole Cell Biocatalyst and Evaluation of Their Antimicrobial Effects
Highly Enantioselective Production of Chiral Secondary Alcohols Using Lactobacillus paracasei BD101 as a New Whole Cell Biocatalyst and Evaluation of Their Antimicrobial Effects
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Highly Enantioselective Production of Chiral Secondary Alcohols Using Lactobacillus paracasei BD101 as a New Whole Cell Biocatalyst and Evaluation of Their Antimicrobial Effects

Yılmaz, Durmuşhan ; Şahin, Engin ; Dertli, Enes

Chemistry & biodiversity, 2017-11, Vol.14 (11), p.n/a [Periódico revisado por pares]

Switzerland

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12
Nickel‐Catalyzed Intermolecular Asymmetric Addition of Aryl Iodides across Aldehydes
Nickel‐Catalyzed Intermolecular Asymmetric Addition of Aryl Iodides across Aldehydes
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Nickel‐Catalyzed Intermolecular Asymmetric Addition of Aryl Iodides across Aldehydes

Zhu, Ziqi ; Xiao, Jieshuai ; Li, Mingjie ; Shi, Zhuangzhi

Angewandte Chemie (International ed.), 2022-05, Vol.61 (20), p.e202201370-n/a [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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13
Biocatalytic properties of a recombinant aldo-keto reductase with broad substrate spectrum and excellent stereoselectivity
Biocatalytic properties of a recombinant aldo-keto reductase with broad substrate spectrum and excellent stereoselectivity
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Biocatalytic properties of a recombinant aldo-keto reductase with broad substrate spectrum and excellent stereoselectivity

Ni, Yan ; Li, Chun-Xiu ; Ma, Hong-Min ; Zhang, Jie ; Xu, Jian-He

Applied microbiology and biotechnology, 2011-02, Vol.89 (4), p.1111-1118 [Periódico revisado por pares]

Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag

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14
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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15
Two anti‐Prelog NAD‐Dependent Alcohol Dehydrogenases with Broad Substrate Scope and Excellent Enantioselectivity
Two anti‐Prelog NAD‐Dependent Alcohol Dehydrogenases with Broad Substrate Scope and Excellent Enantioselectivity
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Two anti‐Prelog NAD‐Dependent Alcohol Dehydrogenases with Broad Substrate Scope and Excellent Enantioselectivity

Damian, Matteo ; Mutti, Francesco G.

European journal of organic chemistry, 2023-12, Vol.26 (47), p.n/a [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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16
Combined Photoredox/Enzymatic C−H Benzylic Hydroxylations
Combined Photoredox/Enzymatic C−H Benzylic Hydroxylations
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Combined Photoredox/Enzymatic C−H Benzylic Hydroxylations

Betori, Rick C. ; May, Catherine M. ; Scheidt, Karl A.

Angewandte Chemie (International ed.), 2019-11, Vol.58 (46), p.16490-16494 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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17
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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18
Kinetic Resolution of Secondary Alcohols Catalyzed by Chiral Phosphoric Acids
Kinetic Resolution of Secondary Alcohols Catalyzed by Chiral Phosphoric Acids
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Kinetic Resolution of Secondary Alcohols Catalyzed by Chiral Phosphoric Acids

Harada, Shingo ; Kuwano, Satoru ; Yamaoka, Yousuke ; Yamada, Ken-ichi ; Takasu, Kiyosei

Angewandte Chemie (International ed.), 2013-09, Vol.52 (39), p.10227-10230 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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19
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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20
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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Deste Autor:

  1. Andrade, L
  2. Araújo, L

Neste Assunto:

  1. Chiral Alcohols
  2. Chiral Alcohols
  3. Science & Technology
  4. Chemistry
  5. Physical Sciences

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