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Dual Enantioselective Control using D-phenylglycine-L-proline-derived Catalysts for the Enantioselective Addition of Diethylzinc to Aldehyde

Bulletin of the Korean Chemical Society, 2016, 37(1), , pp.108-111

2016

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Asymmetric Preparation of D-Phg-L-Pro Dipeptide-derived Chiral Ligands for Enantioselective Addition of Diethylzinc to Aldehydes

Bulletin of the Korean Chemical Society, 2012, 33(7), , pp.2397-2400

2012

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L-Alanine-derived Chiral Ligands for Asymmetric Addition of Diethylzinc to Aldehydes

Bulletin of the Korean Chemical Society, 2012, 33(9), , pp.3125-3128

2012

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Discovery of Dipeptide-Derived Catalysts for the Enantioselective Addition of Dimethylzinc to Aldehydes

European Journal of Organic Chemistry, 2012-03, Vol.2012 (9), p.1703-1706

2012

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Dynamic resolution of α-halo chiral esters for the synthesis of 3-substituted piperazin-2-ones

Tetrahedron, 2011-08, Vol.67 (34), p.6221-6226

2011

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Progerinin, an optimized progerin-lamin A binding inhibitor, ameliorates premature senescence phenotypes of Hutchinson-Gilford progeria syndrome

Communications biology, 2021-01, Vol.4 (1), p.5-5, Article 5

2021

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Author Correction: Progerinin, an optimized progerin-lamin A binding inhibitor, ameliorates premature senescence phenotypes of Hutchinson-Gilford progeria syndrome

Communications biology, 2021-03, Vol.4 (1), p.297-297, Article 297

2021

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An Efficient Synthesis of an Apoptosis Inducer, F-3-2-5 by Using Octanol-Accelerated Baylis-Hillman Reaction

Bulletin of the Korean Chemical Society, 2007, 28(2), , pp.179-180

2007

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Effects of the aryl linker and the aromatic substituent on the anti-HCV activities of aryl diketoacid (ADK) analogues

Bioorganic & medicinal chemistry, 2008-08, Vol.18 (16), p.4661-4665

2008

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Prediction of the Antagonistic Activity of Aryl Benzyl Ethers against LTD4 by Using 3D-CoMFA Model Developed with Pranlukast Analogues

Bulletin of the Korean Chemical Society, 2006-07, Vol.27 (7), p.1025-1030

2006

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Prediction of the Antagonistic Activity of Aryl Benzyl Ethers against LTD4 by Using 3D-CoMFA Model Developed with Pranlukast Analogues

Bulletin of the Korean Chemical Society, 2006, 27(7), , pp.1025-1030

2006

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Synthesis of Naringenin Amino Acid Esters as Potential CDK2 Inhibitors

Bulletin of the Korean Chemical Society, 2005, 26(12), , pp.2065-2068

2005

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Discovery of a potent dual ALK and EGFR T790M inhibitor

European journal of medicinal chemistry, 2017-08, Vol.136, p.497-510

2017

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Asymmetric Synthesis of 3,4,6-Trisubstituted 2,5-Diketopiperazines by Using Dynamic Kinetic Resolution of α-Bromo Tertiary Acetamides

European journal of organic chemistry, 2014-05, Vol.2014 (13), p.2780-2789

2014

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Asymmetric Synthesis of 3,4,6-Trisubstituted 2,5-Diketopiperazines by Using Dynamic Kinetic Resolution of [alpha]-Bromo Tertiary Acetamides

European journal of organic chemistry, 2014-05, Vol.2014 (13), p.2780

2014

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L-Alanine-derived Chiral Ligands for Asymmetric Addition of Diethylzinc to Aldehydes

Bulletin of the Korean Chemical Society, 2012, Vol.33 (9), p.3125-3128

2012

Volltextzugriff (PDF)

Asymmetric Preparation of D-Phg-L-Pro Dipeptide-derived Chiral Ligands for Enantioselective Addition of Diethylzinc to Aldehydes

Bulletin of the Korean Chemical Society, 2012, Vol.33 (7), p.2397-2400

2012

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Abstract 5477: Compound A, a fourth-generation allosteric inhibitor, a potent and highly selective EGFR with L858R activating and C797S resistance mutations for the treatment of NSCLC

Cancer research (Chicago, Ill.), 2022-06, Vol.82 (12_Supplement), p.5477-5477

2022

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An Efficient Synthesis of an Apoptosis Inducer, F-3-2-5 by Using Octanol-Accelerated Baylis-Hillman Reaction

Bulletin of the Korean Chemical Society, 2007, Vol.28 (2), p.179-180

2007

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ChemInform Abstract: Dual Enantioselective Control Using D‐Phenylglycine‐L‐Proline‐Derived Catalysts for the Enantioselective Addition of Diethylzinc to Aldehyde

ChemInform, 2016-05, Vol.47 (21), p.no-no

2016

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Synthesis of Naringenin Amino Acid Esters as Potential CDK2 Inhibitors

Bulletin of the Korean Chemical Society, 2005-12, Vol.26 (12), p.2065-2068

2005

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ChemInform Abstract: Discovery of Dipeptide-Derived Catalysts for the Enantioselective Addition of Dimethylzinc to Aldehydes

ChemInform, 2012-08, Vol.43 (32), p.no-no

2012

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ChemInform Abstract: Asymmetric Preparation of New N,N-Dialkyl-2-amino-1,1,2-triphenylethanol Catalysts and a Kinetic Resolution in the Addition of Diethylzinc to Flavene-3-carbaldehydes

ChemInform, 2013-07, Vol.44 (28), p.no-no

2013

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ChemInform Abstract: Dynamic Resolution of α-Halo Chiral Esters for the Synthesis of 3-Substituted Piperazin-2-ones

ChemInform, 2011-12, Vol.42 (52), p.no-no

2011

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Dual Enantioselective Control using D-phenylglycine-L-proline-derived Catalysts for the Enantioselective Addition of Diethylzinc to Aldehyde

Asymmetric Preparation of D-Phg-L-Pro Dipeptide-derived Chiral Ligands for Enantioselective Addition of Diethylzinc to Aldehydes

L-Alanine-derived Chiral Ligands for Asymmetric Addition of Diethylzinc to Aldehydes

Discovery of Dipeptide-Derived Catalysts for the Enantioselective Addition of Dimethylzinc to Aldehydes

Dynamic resolution of α-halo chiral esters for the synthesis of 3-substituted piperazin-2-ones

Progerinin, an optimized progerin-lamin A binding inhibitor, ameliorates premature senescence phenotypes of Hutchinson-Gilford progeria syndrome

Author Correction: Progerinin, an optimized progerin-lamin A binding inhibitor, ameliorates premature senescence phenotypes of Hutchinson-Gilford progeria syndrome

An Efficient Synthesis of an Apoptosis Inducer, F-3-2-5 by Using Octanol-Accelerated Baylis-Hillman Reaction

Effects of the aryl linker and the aromatic substituent on the anti-HCV activities of aryl diketoacid (ADK) analogues

Prediction of the Antagonistic Activity of Aryl Benzyl Ethers against LTD4 by Using 3D-CoMFA Model Developed with Pranlukast Analogues

Prediction of the Antagonistic Activity of Aryl Benzyl Ethers against LTD4 by Using 3D-CoMFA Model Developed with Pranlukast Analogues

Synthesis of Naringenin Amino Acid Esters as Potential CDK2 Inhibitors

Discovery of a potent dual ALK and EGFR T790M inhibitor

Asymmetric Synthesis of 3,4,6-Trisubstituted 2,5-Diketopiperazines by Using Dynamic Kinetic Resolution of α-Bromo Tertiary Acetamides

Asymmetric Synthesis of 3,4,6-Trisubstituted 2,5-Diketopiperazines by Using Dynamic Kinetic Resolution of [alpha]-Bromo Tertiary Acetamides

L-Alanine-derived Chiral Ligands for Asymmetric Addition of Diethylzinc to Aldehydes

Asymmetric Preparation of D-Phg-L-Pro Dipeptide-derived Chiral Ligands for Enantioselective Addition of Diethylzinc to Aldehydes

Abstract 5477: Compound A, a fourth-generation allosteric inhibitor, a potent and highly selective EGFR with L858R activating and C797S resistance mutations for the treatment of NSCLC

An Efficient Synthesis of an Apoptosis Inducer, F-3-2-5 by Using Octanol-Accelerated Baylis-Hillman Reaction

ChemInform Abstract: Dual Enantioselective Control Using D‐Phenylglycine‐L‐Proline‐Derived Catalysts for the Enantioselective Addition of Diethylzinc to Aldehyde

Synthesis of Naringenin Amino Acid Esters as Potential CDK2 Inhibitors

ChemInform Abstract: Discovery of Dipeptide-Derived Catalysts for the Enantioselective Addition of Dimethylzinc to Aldehydes

ChemInform Abstract: Asymmetric Preparation of New N,N-Dialkyl-2-amino-1,1,2-triphenylethanol Catalysts and a Kinetic Resolution in the Addition of Diethylzinc to Flavene-3-carbaldehydes

ChemInform Abstract: Dynamic Resolution of α-Halo Chiral Esters for the Synthesis of 3-Substituted Piperazin-2-ones

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