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Potent and Selective Mitogen-Activated Protein Kinase Kinase (MEK) 1,2 Inhibitors. 1. 4-(4-Bromo-2-fluorophenylamino)-1- methylpyridin-2(1H)-ones

Journal of medicinal chemistry, 2006-01, Vol.49 (2), p.441-444

2006

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Potent, low-calcemic, selective inhibitors of CYP24 hydroxylase: 24-sulfone analogs of the hormone 1α, 25-dihydroxyvitamin D3

Journal of steroid biochemistry and molecular biology, 2004-05, Vol.89-90 (1-5), p.5-12

2004

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Synthesis and bioactivities of steroid derivatives as antifungal agents

Tetrahedron, 1998-12, Vol.54 (52), p.15899-15914

1998

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Methods for the synthesis of optically active β-lactones (2-oxetanones)

Tetrahedron, 1999-05, Vol.55 (21), p.6403-6434

1999

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Mechanism and Origin of Stereoselectivity in Lewis Acid Catalyzed [2+2] Cycloadditions of Ketenes with Aldehydes

Angewandte Chemie International Edition, 2002-05, Vol.41 (9), p.1572-1575

2002

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Studies of the tandem Mukaiyama aldol-lactonization (TMAL) reaction: A concise and highly diastereoselective route to β-lactones applied to the total synthesis of the potent pancreatic lipase inhibitor, (−)-Panclicin D

Tetrahedron, 1997-12, Vol.53 (48), p.16471-16488

1997

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Studies of the asymmetric [2+2] cycloaddition of silylketenes and aldehydes employing Ti-TADDOL catalysts

Tetrahedron letters, 1998-05, Vol.39 (19), p.2877-2880

1998

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Potent, low-calcemic, selective inhibitors of CYP24 hydroxylase: 24-sulfone analogs of the hormone 1α,25-dihydroxyvitamin D 3

The Journal of steroid biochemistry and molecular biology, 2004-05, Vol.89, p.5-12

2004

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Corrigendum to Tetrahedron report number 492: “Methods for the synthesis of optically active β-lactones (2-oxetanones)” [Tetrahedron 55 (1999) 6403]

Tetrahedron, 1999-07, Vol.55 (30), p.9347-9347

1999

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A Single-Pot, Mild Conversion of β-Lactones to β-Lactams

Journal of organic chemistry, 1999-10, Vol.64 (20), p.7657-7660

1999

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A Highly Diastereoselective, Tandem Mukaiyama Aldol-Lactonization Route to β-Lactones: Application to a Concise Synthesis of the Potent Pancreatic Lipase Inhibitor, (−)-Panclicin D

Journal of organic chemistry, 1997-01, Vol.62 (1), p.4-5

1997

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Practical, One-Step Synthesis of Optically Active β-Lactones via the Tandem Mukaiyama Aldol−Lactonization (TMAL) Reaction

Journal of organic chemistry, 1998-02, Vol.63 (4), p.1344-1347

1998

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Synthesis and inhibitory action on HMG-CoA synthase of racemic and optically active oxetan-2-ones (β-Lactones)

Bioorganic & medicinal chemistry, 1998-08, Vol.6 (8), p.1255-1272

1998

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Potent, low-calcemic, selective inhibitors of CYP24 hydroxylase: 24-sulfone analogs of the hormone 1alpha,25-dihydroxyvitamin D3

The Journal of steroid biochemistry and molecular biology, 2004-05, Vol.89-90 (1-5), p.5-12

2004

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Mechanism and Origin of Stereoselectivity in Lewis Acid Catalyzed [2+2] Cycloadditions of Ketenes with Aldehydes

Angewandte Chemie, 2002-05, Vol.114 (9), p.1642-1645

2002

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Concise, stereoselective routes to beta-lactones: Application to the synthesis of the potent pancreatic lipase inhibitor, (-)-panclicin D

Yang, Hong Woon

1998

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ChemInform Abstract: A Single-Pot, Mild Conversion of β-Lactones to β-Lactams

ChemInform, 2000-02, Vol.31 (7), p.no-no

2000

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ChemInform Abstract: Methods for the Synthesis of Optically Active β-Lactones (2-Oxetanones)

ChemInform, 1999-09, Vol.30 (36), p.no-no

1999

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Synthetic β-lactam antibiotics VI. Antibacterial activity of some 7β-[-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido]-3-(pyrrolidinium) methylcephalosporins

Archives of pharmacal research, 1992-06, Vol.15 (2), p.187-189

1992

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ChemInform Abstract: Synthesis and Bioactivities of Steroid Derivatives as Antifungal Agents

ChemInform, 1999-04, Vol.30 (17), p.no-no

1999

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Beneficial Effects of PbI2 Incorporated in Organo-Lead Halide Perovskite Solar Cells

Advanced energy materials, 2016-02, Vol.6 (4), p.n/a

2016

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Voltage output of efficient perovskite solar cells with high open-circuit voltage and fill factor

Energy & environmental science, 2014, Vol.7 (8), p.2614-2618

2014

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Iodide management in formamidinium-lead-halide–based perovskite layers for efficient solar cells

Science (American Association for the Advancement of Science), 2017-06, Vol.356 (6345), p.1376-1379

2017

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Thermal Stability of CuSCN Hole Conductor-Based Perovskite Solar Cells

ChemSusChem, 2016-09, Vol.9 (18), p.2592-2596

2016

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High-performance photovoltaic perovskite layers fabricated through intramolecular exchange

Science (American Association for the Advancement of Science), 2015-06, Vol.348 (6240), p.1234-1237

2015

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Potent and Selective Mitogen-Activated Protein Kinase Kinase (MEK) 1,2 Inhibitors. 1. 4-(4-Bromo-2-fluorophenylamino)-1- methylpyridin-2(1H)-ones

Potent, low-calcemic, selective inhibitors of CYP24 hydroxylase: 24-sulfone analogs of the hormone 1α, 25-dihydroxyvitamin D3

Synthesis and bioactivities of steroid derivatives as antifungal agents

Methods for the synthesis of optically active β-lactones (2-oxetanones)

Mechanism and Origin of Stereoselectivity in Lewis Acid Catalyzed [2+2] Cycloadditions of Ketenes with Aldehydes

Studies of the tandem Mukaiyama aldol-lactonization (TMAL) reaction: A concise and highly diastereoselective route to β-lactones applied to the total synthesis of the potent pancreatic lipase inhibitor, (−)-Panclicin D

Studies of the asymmetric [2+2] cycloaddition of silylketenes and aldehydes employing Ti-TADDOL catalysts

Potent, low-calcemic, selective inhibitors of CYP24 hydroxylase: 24-sulfone analogs of the hormone 1α,25-dihydroxyvitamin D 3

Corrigendum to Tetrahedron report number 492: “Methods for the synthesis of optically active β-lactones (2-oxetanones)” [Tetrahedron 55 (1999) 6403]

A Single-Pot, Mild Conversion of β-Lactones to β-Lactams

A Highly Diastereoselective, Tandem Mukaiyama Aldol-Lactonization Route to β-Lactones: Application to a Concise Synthesis of the Potent Pancreatic Lipase Inhibitor, (−)-Panclicin D

Practical, One-Step Synthesis of Optically Active β-Lactones via the Tandem Mukaiyama Aldol−Lactonization (TMAL) Reaction

Synthesis and inhibitory action on HMG-CoA synthase of racemic and optically active oxetan-2-ones (β-Lactones)

Potent, low-calcemic, selective inhibitors of CYP24 hydroxylase: 24-sulfone analogs of the hormone 1alpha,25-dihydroxyvitamin D3

Mechanism and Origin of Stereoselectivity in Lewis Acid Catalyzed [2+2] Cycloadditions of Ketenes with Aldehydes

Concise, stereoselective routes to beta-lactones: Application to the synthesis of the potent pancreatic lipase inhibitor, (-)-panclicin D

ChemInform Abstract: A Single-Pot, Mild Conversion of β-Lactones to β-Lactams

ChemInform Abstract: Methods for the Synthesis of Optically Active β-Lactones (2-Oxetanones)

Synthetic β-lactam antibiotics VI. Antibacterial activity of some 7β-[-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido]-3-(pyrrolidinium) methylcephalosporins

ChemInform Abstract: Synthesis and Bioactivities of Steroid Derivatives as Antifungal Agents

Beneficial Effects of PbI2 Incorporated in Organo-Lead Halide Perovskite Solar Cells

Voltage output of efficient perovskite solar cells with high open-circuit voltage and fill factor

Iodide management in formamidinium-lead-halide–based perovskite layers for efficient solar cells

Thermal Stability of CuSCN Hole Conductor-Based Perovskite Solar Cells

High-performance photovoltaic perovskite layers fabricated through intramolecular exchange

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