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Biocatalytic reductive desymmetrization of prochiral 1,3-diketone and its application to microbial hormone synthesis

Molecular catalysis, 2020-12, Vol.497, p.111217, Article 111217

2020

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Characterization of a novel hydroxynitrile lyase from Nandina domestica Thunb

Bioscience, biotechnology, and biochemistry, 2018-10, Vol.82 (10), p.1760-1769

2018

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Isolation and characterization of racemase from Ensifer sp. 23-3 that acts on α-aminolactams and α-amino acid amides

Journal of industrial microbiology & biotechnology, 2017-11, Vol.44 (11), p.1503-1510

2017

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Synthesis of ( R)-β-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous–organic biphasic system

Journal of biotechnology, 2011-05, Vol.153 (3), p.153-159

2011

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First total synthesis of modiolide A, based on the whole-cell yeast-catalyzed asymmetric reduction of a propargyl ketone

Tetrahedron, 2007-09, Vol.63 (36), p.8752-8760

2007

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Synthesis of two piperidine alkaloids, (−)-deoxoprosopinine and (−)-deoxoprosophylline, from 6-hydroxylated dihydrosphingosine derivatives

Tetrahedron: asymmetry, 2007-09, Vol.18 (17), p.2104-2107

2007

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Trans Fatty Acid Intake and Serum Cholesterol Levels in Young Japanese Women

Bioscience, biotechnology, and biochemistry, 2012, Vol.76 (9), p.1627-1632

2012

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A novel S-enantioselective amidase acting on 3,3,3-trifluoro-2-hydroxy-2-methylpropanamide from Arthrobacter sp. S-2

Bioscience, biotechnology, and biochemistry, 2015-10, Vol.79 (10), p.1587-1596

2015

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Enantiomerically Pure Octahydronaphthalenone and Octahydroindenone: Elaboration of the Substrate Overcame the Specificity of Yeast-Mediated Reduction

Advanced synthesis & catalysis, 2003-06, Vol.345 (6-7), p.766-774

2003

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A Simple Enzymatic Method for Production of a Wide Variety of _D-Amino Acids Using _L-Amino Acid Oxidase from Rhodococcus sp. AIU Z-35-1

Enzyme Research, 2010-08, Vol.2010, p.567210-6

2010

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Screening, substrate specificity and stereoselectivity of yeast strains, which reduce sterically hindered isopropyl ketones

Tetrahedron: asymmetry, 2006-12, Vol.17 (24), p.3358-3367

2006

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S-selective hydroxynitrile lyase from a plant Baliospermum montanum: Molecular characterization of recombinant enzyme

Journal of biotechnology, 2011-05, Vol.153 (3), p.100-110

2011

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Efficient preparation of both enantiomers of 3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid catalyzed by Shinella sp. R-6 and Arthrobacter sp. S-2

Journal of molecular catalysis. B, Enzymatic, 2014-04, Vol.102, p.115-119

2014

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Chemoenzymatic Route to Both Enantiomers of a 1-Isopropyl-3a-methyloctahydroinden-4-one Derivative: A Synthetic Intermediate for Sesqui- and Diterpenoids

Advanced synthesis & catalysis, 2005-06, Vol.347 (7-8), p.1099-1109

2005

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Unprecedented chemo-enzymatic synthesis of stereochemically pure 3-acetoxy-2-methyl-2-vinylcycloalkanones

Tetrahedron letters, 2004-02, Vol.45 (8), p.1763-1767

2004

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RCAI-8, 9, 18, 19, and 49–52, conformationally restricted analogues of KRN7000 with an azetidine or a pyrrolidine ring: Their synthesis and bioactivity for mouse natural killer T cells to produce cytokines

Bioorganic & medicinal chemistry, 2008-01, Vol.16 (2), p.950-964

2008

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Formal Synthesis of (+)-Madindoline A a Potent IL-6 Inhibitor Utilizing Enzymatic Discrimination of Quaternary Carbon

Natural product communications, 2013-07, Vol.8 (7), p.897-901

2013

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Preparation of d-α-aminolactams by l-enantioselective degradation of α-aminolactam mediated by Mesorhizobium sp. L88

Biocatalysis and agricultural biotechnology, 2014-07, Vol.3 (3), p.42-47

2014

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Access to Enantiomerically Pure Intermediates for (−)-Geosmin Synthesis Starting from (4aS,5S)-4,4a,5,6,7,8-Hexahydro-5-hydroxy-4a-methyl-naphthalen-2(3H)-one

Bioscience, biotechnology, and biochemistry, 2002-01, Vol.66 (10), p.2267-2272

2002

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Application to the Preparation of Useful Compounds Based on Enzyme-and Microorganism-mediated Reactions

Journal of Synthetic Organic Chemistry, Japan, 2006/06/01, Vol.64(6), pp.664-676

2006

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Realization of the synthesis of α,α-disubstituted carbamylacetates and cyanoacetates by either enzymatic or chemical functional group transformation, depending upon the substrate specificity of Rhodococcus amidase

Tetrahedron: asymmetry, 2004-09, Vol.15 (18), p.2817-2820

2004

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Control of the nitrile-hydrolyzing enzyme activity in Rhodococcus rhodochrous IFO 15564: preferential action of nitrile hydratase and amidase depending on the reaction condition factors and its application to the one-pot preparation of amides from aldehydes

Journal of molecular catalysis. B, Enzymatic, 2004-06, Vol.29 (1-6), p.249-258

2004

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Access to Wieland−Miescher Ketone in an Enantiomerically Pure Form by a Kinetic Resolution with Yeast-Mediated Reduction

Journal of organic chemistry, 2000-01, Vol.65 (1), p.129-135

2000

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Access to enantiomerically pure intermediates for (-)-geosmin synthesis starting from (4aS, 5S)-4,4a, 5,6,7,8-hexahydro-5-hydroxy-4a-methylnaphthalen-2(3 H)-one

Bioscience, biotechnology, and biochemistry, 2002-10, Vol.66 (10), p.2267-2272

2002

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Efficient preparation of both enantiomers of 3,3,3-trilfuoro-2-hydroxy-2-methylpropanoic acid catalyzed by Shinella sp. R-6 and Arthrobacter sp. S-2

Journal of molecular catalysis. B, Enzymatic, 2014, Vol.102, p.115-119

2014

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Biocatalytic reductive desymmetrization of prochiral 1,3-diketone and its application to microbial hormone synthesis

Characterization of a novel hydroxynitrile lyase from Nandina domestica Thunb

Isolation and characterization of racemase from Ensifer sp. 23-3 that acts on α-aminolactams and α-amino acid amides

Synthesis of ( R)-β-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous–organic biphasic system

First total synthesis of modiolide A, based on the whole-cell yeast-catalyzed asymmetric reduction of a propargyl ketone

Synthesis of two piperidine alkaloids, (−)-deoxoprosopinine and (−)-deoxoprosophylline, from 6-hydroxylated dihydrosphingosine derivatives

Trans Fatty Acid Intake and Serum Cholesterol Levels in Young Japanese Women

A novel S-enantioselective amidase acting on 3,3,3-trifluoro-2-hydroxy-2-methylpropanamide from Arthrobacter sp. S-2

Enantiomerically Pure Octahydronaphthalenone and Octahydroindenone: Elaboration of the Substrate Overcame the Specificity of Yeast-Mediated Reduction

A Simple Enzymatic Method for Production of a Wide Variety of _D-Amino Acids Using _L-Amino Acid Oxidase from Rhodococcus sp. AIU Z-35-1

Screening, substrate specificity and stereoselectivity of yeast strains, which reduce sterically hindered isopropyl ketones

S-selective hydroxynitrile lyase from a plant Baliospermum montanum: Molecular characterization of recombinant enzyme

Efficient preparation of both enantiomers of 3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid catalyzed by Shinella sp. R-6 and Arthrobacter sp. S-2

Chemoenzymatic Route to Both Enantiomers of a 1-Isopropyl-3a-methyloctahydroinden-4-one Derivative: A Synthetic Intermediate for Sesqui- and Diterpenoids

Unprecedented chemo-enzymatic synthesis of stereochemically pure 3-acetoxy-2-methyl-2-vinylcycloalkanones

RCAI-8, 9, 18, 19, and 49–52, conformationally restricted analogues of KRN7000 with an azetidine or a pyrrolidine ring: Their synthesis and bioactivity for mouse natural killer T cells to produce cytokines

Formal Synthesis of (+)-Madindoline A a Potent IL-6 Inhibitor Utilizing Enzymatic Discrimination of Quaternary Carbon

Preparation of d-α-aminolactams by l-enantioselective degradation of α-aminolactam mediated by Mesorhizobium sp. L88

Access to Enantiomerically Pure Intermediates for (−)-Geosmin Synthesis Starting from (4aS,5S)-4,4a,5,6,7,8-Hexahydro-5-hydroxy-4a-methyl-naphthalen-2(3H)-one

Application to the Preparation of Useful Compounds Based on Enzyme-and Microorganism-mediated Reactions

Realization of the synthesis of α,α-disubstituted carbamylacetates and cyanoacetates by either enzymatic or chemical functional group transformation, depending upon the substrate specificity of Rhodococcus amidase

Control of the nitrile-hydrolyzing enzyme activity in Rhodococcus rhodochrous IFO 15564: preferential action of nitrile hydratase and amidase depending on the reaction condition factors and its application to the one-pot preparation of amides from aldehydes

Access to Wieland−Miescher Ketone in an Enantiomerically Pure Form by a Kinetic Resolution with Yeast-Mediated Reduction

Access to enantiomerically pure intermediates for (-)-geosmin synthesis starting from (4aS, 5S)-4,4a, 5,6,7,8-hexahydro-5-hydroxy-4a-methylnaphthalen-2(3 H)-one

Efficient preparation of both enantiomers of 3,3,3-trilfuoro-2-hydroxy-2-methylpropanoic acid catalyzed by Shinella sp. R-6 and Arthrobacter sp. S-2

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