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The Modified Mosher’s Method and the Sulfoximine Method

Bulletin of the Chemical Society of Japan, 2006-07, Vol.79 (7), p.965-980

2006

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Phenylglycine Methyl Ester, a Useful Tool for Absolute Configuration Determination of Various Chiral Carboxylic Acids

Journal of organic chemistry, 2000-01, Vol.65 (2), p.397-404

2000

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NMR Spectroscopic Determination of the Absolute Configuration of Chiral Sulfoxides via N-(Methoxyphenylacetyl)sulfoximines

Journal of the American Chemical Society, 1999-11, Vol.121 (45), p.10646-10647

1999

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Discovery of novel indole derivatives as potent and selective inhibitors of proMMP-9 activation

Bioorganic & medicinal chemistry letters, 2024-01, Vol.97, p.129541-129541, Article 129541

2024

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Chiral Anisotropic Reagents for Determining the Absolute Configuration of Secondary Alcohols and Carboxylic Acids

Journal of Synthetic Organic Chemistry, Japan, 2005/11/01, Vol.63(11), pp.1102-1114

2005

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Discovery and optimization of a series of 2-aminothiazole-oxazoles as potent phosphoinositide 3-kinase γ inhibitors

Bioorganic & medicinal chemistry letters, 2012-12, Vol.22 (24), p.7534-7538

2012

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Discovery of N-{5-[3-(3-hydroxypiperidin-1-yl)-1,2,4-oxadiazol-5-yl]-4-methyl-1,3-thiazol-2-yl}acetamide (TASP0415914) as an orally potent phosphoinositide 3-kinase γ inhibitor for the treatment of inflammatory diseases

Bioorganic & medicinal chemistry, 2013-12, Vol.21 (24), p.7578-7583

2013

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A CONVENIENT SYNTHESIS OF 2-MERCAPTO-OXAZOLES VIA β-KETOAZIDE AND ITS APPLICATION TO A KEY INTERMEDIATE OF PI3Kγ INHIBITORS

Heterocycles, 2013, Vol.87 (9), p.1881

2013

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5-(1,3-Benzothiazol-6-yl)-4-(4-methyl-1,3-thiazol-2-yl)-1H-imidazole derivatives as potent and selective transforming growth factor-β type I receptor inhibitors

Bioorganic & medicinal chemistry, 2012-12, Vol.20 (24), p.7128-7138

2012

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A Convenient One-Pot Synthesis of Quaternary α-Methoxy- and α-Hydroxycarboxylic Acids

Chemical and Pharmaceutical Bulletin, 1999/05/15, Vol.47(5), pp.684-686

1999

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Pyrrole derivatives as potent inhibitors of lymphocyte-specific kinase: Structure, synthesis, and SAR

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (1), p.108-111

2010

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Discovery and optimization of a series of 2-aminothiazole-oxazoles as potent phosphoinositide 3-kinase [gamma] inhibitors

Bioorganic & medicinal chemistry letters, 2012-12, Vol.22 (24), p.7534-7538

2012

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5-(1,3-Benzothiazol-6-yl)-4-(4-methyl-1,3-thiazol-2-yl)-1H-imidazo le derivatives as potent and selective transforming growth factor-[beta] type I receptor inhibitors

Bioorganic & medicinal chemistry, 2012-12, Vol.20 (24), p.7128-7138

2012

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Ring-fused pyrazole derivatives as potent inhibitors of lymphocyte-specific kinase (Lck): Structure, synthesis, and SAR

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (1), p.112-116

2010

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Application of phenylglycine methyl ester (PGME) to determination of the absolute configuration of carboxylic acids having phenylalkyl group

Chirality (New York, N.Y.), 1997, Vol.9 (5-6), p.550-555

1997

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Resolution of 1- and 2-naphthylmethoxyacetic acids, NMR reagents for absolute configuration determination, by use of L-phenylalaninol

Chirality (New York, N.Y.), 2003, Vol.15 (7), p.609-614

2003

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A Convenient One-Pot Synthesis of Quaternary [alpha]-Methoxy- and [alpha]-Hydroxycarboxylic Acids

Chemical & pharmaceutical bulletin, 1999-05, Vol.47 (5), p.684

1999

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Sesquiterpenes and Monoterpenes from the Bark of Inula macrophylla

Journal of natural products (Washington, D.C.), 2001-04, Vol.64 (4), p.466-471

2001

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ChemInform Abstract: A Convenient Synthesis of 2-Mercapto-oxazoles via [beta]-Ketoazide and Its Application to a Key Intermediate of PI3K[gamma] Inhibitors

ChemInform, 2014-01, Vol.45 (4)

2014

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ChemInform Abstract: A Convenient Synthesis of 2-Mercapto-oxazoles via β-Ketoazide and Its Application to a Key Intermediate of PI3Kγ Inhibitors

ChemInform, 2014-01, Vol.45 (4), p.no-no

2014

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The structures and absolute configurations of macrophyllic acids A–E, five new rearranged eudesmane sesquiterpene acids from the bark of Inula macrophylla

Tetrahedron letters, 2000-04, Vol.41 (14), p.2395-2400

2000

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Sesquiterpenes and Monoterpenes from the Bark of Inula m acrophylla

Journal of natural products (Washington, D.C.), 2001-04, Vol.64 (4), p.466-471

2001

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ChemInform Abstract: A Convenient One-Pot Synthesis of Quaternary α-Methoxy- and α-Hydroxycarboxylic Acids

ChemInform, 1999-11, Vol.30 (45), p.no-no

1999

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The Modified Mosher′s Method and the Sulfoximine Method

ChemInform, 2006-10, Vol.37 (44), p.no-no

2006

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Chiral Anisotropic Reagents for Determining the Absolute Configuration of Secondary Alcohols and Carboxylic Acids

ChemInform, 2006-05, Vol.37 (18), p.no-no

2006

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The Modified Mosher’s Method and the Sulfoximine Method

Phenylglycine Methyl Ester, a Useful Tool for Absolute Configuration Determination of Various Chiral Carboxylic Acids

NMR Spectroscopic Determination of the Absolute Configuration of Chiral Sulfoxides via N-(Methoxyphenylacetyl)sulfoximines

Discovery of novel indole derivatives as potent and selective inhibitors of proMMP-9 activation

Chiral Anisotropic Reagents for Determining the Absolute Configuration of Secondary Alcohols and Carboxylic Acids

Discovery and optimization of a series of 2-aminothiazole-oxazoles as potent phosphoinositide 3-kinase γ inhibitors

Discovery of N-{5-[3-(3-hydroxypiperidin-1-yl)-1,2,4-oxadiazol-5-yl]-4-methyl-1,3-thiazol-2-yl}acetamide (TASP0415914) as an orally potent phosphoinositide 3-kinase γ inhibitor for the treatment of inflammatory diseases

A CONVENIENT SYNTHESIS OF 2-MERCAPTO-OXAZOLES VIA β-KETOAZIDE AND ITS APPLICATION TO A KEY INTERMEDIATE OF PI3Kγ INHIBITORS

5-(1,3-Benzothiazol-6-yl)-4-(4-methyl-1,3-thiazol-2-yl)-1H-imidazole derivatives as potent and selective transforming growth factor-β type I receptor inhibitors

A Convenient One-Pot Synthesis of Quaternary α-Methoxy- and α-Hydroxycarboxylic Acids

Pyrrole derivatives as potent inhibitors of lymphocyte-specific kinase: Structure, synthesis, and SAR

Discovery and optimization of a series of 2-aminothiazole-oxazoles as potent phosphoinositide 3-kinase [gamma] inhibitors

5-(1,3-Benzothiazol-6-yl)-4-(4-methyl-1,3-thiazol-2-yl)-1H-imidazo le derivatives as potent and selective transforming growth factor-[beta] type I receptor inhibitors

Ring-fused pyrazole derivatives as potent inhibitors of lymphocyte-specific kinase (Lck): Structure, synthesis, and SAR

Application of phenylglycine methyl ester (PGME) to determination of the absolute configuration of carboxylic acids having phenylalkyl group

Resolution of 1- and 2-naphthylmethoxyacetic acids, NMR reagents for absolute configuration determination, by use of L-phenylalaninol

A Convenient One-Pot Synthesis of Quaternary [alpha]-Methoxy- and [alpha]-Hydroxycarboxylic Acids

Sesquiterpenes and Monoterpenes from the Bark of Inula macrophylla

ChemInform Abstract: A Convenient Synthesis of 2-Mercapto-oxazoles via [beta]-Ketoazide and Its Application to a Key Intermediate of PI3K[gamma] Inhibitors

ChemInform Abstract: A Convenient Synthesis of 2-Mercapto-oxazoles via β-Ketoazide and Its Application to a Key Intermediate of PI3Kγ Inhibitors

The structures and absolute configurations of macrophyllic acids A–E, five new rearranged eudesmane sesquiterpene acids from the bark of Inula macrophylla

Sesquiterpenes and Monoterpenes from the Bark of Inula m acrophylla

ChemInform Abstract: A Convenient One-Pot Synthesis of Quaternary α-Methoxy- and α-Hydroxycarboxylic Acids

The Modified Mosher′s Method and the Sulfoximine Method

Chiral Anisotropic Reagents for Determining the Absolute Configuration of Secondary Alcohols and Carboxylic Acids

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