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Efficient Synthesis of Imidazoles from Aldehydes and 1,2-Diketones Using Microwave Irradiation

Organic letters, 2004-04, Vol.6 (9), p.1453-1456

2004

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Allosteric Akt (PKB) inhibitors: discovery and SAR of isozyme selective inhibitors

Bioorganic & medicinal chemistry letters, 2005-02, Vol.15 (3), p.761-764

2005

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General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines

Tetrahedron letters, 2004-06, Vol.45 (25), p.4873-4876

2004

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Discovery of 2,3,5-trisubstituted pyridine derivatives as potent Akt1 and Akt2 dual inhibitors

Bioorganic & medicinal chemistry letters, 2005-02, Vol.15 (4), p.905-909

2005

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Discovery of N-{[1-(propylsulfonyl)-4-pyridin-2-ylpiperidin-4-yl]methyl}benzamides as novel, selective and potent GlyT1 inhibitors

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (5), p.1488-1491

2009

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Structure activity relationships of human galactokinase inhibitors

Bioorganic & medicinal chemistry letters, 2015-02, Vol.25 (3), p.721-727

2015

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Discovery of Positive Allosteric Modulators for the Metabotropic Glutamate Receptor Subtype 5 from a Series of N-(1,3-Diphenyl-1H- pyrazol-5-yl)benzamides That Potentiate Receptor Function in Vivo

Journal of medicinal chemistry, 2004-11, Vol.47 (24), p.5825-5828

2004

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Fluorous-tethered amine bases for organic and parallel synthesis: scope and limitations

Tetrahedron letters, 2002-09, Vol.43 (36), p.6319-6323

2002

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A ‘one pot’ microwave-mediated synthesis of the basic canthine skeleton: expedient access to unnatural β-carboline alkaloids

Tetrahedron letters, 2003-06, Vol.44 (24), p.4495-4498

2003

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Discovery of GlyT1 inhibitors with improved pharmacokinetic properties

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (5), p.1492-1495

2009

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Synthesis and biological evaluation of unnatural canthine alkaloids

Tetrahedron letters, 2005-04, Vol.46 (16), p.2779-2782

2005

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A general Staudinger protocol for solution-phase parallel synthesis

Tetrahedron letters, 2002-06, Vol.43 (25), p.4467-4470

2002

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Design, Synthesis, and Tripeptidyl Peptidase II Inhibitory Activity of a Novel Series of (S)-2,3-Dihydro-2-(4-alkyl-1H-imidazol-2-yl)-1H-indoles

Journal of medicinal chemistry, 2002-11, Vol.45 (24), p.5303-5310

2002

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Broadening the scope of 1,2,4-triazine synthesis by the application of microwave technology

Tetrahedron letters, 2003-02, Vol.44 (6), p.1123-1127

2003

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Analysis and purification of modified methoxy(polyethylene glycol) compounds of similar molecular mass by high-performance liquid chromatography

Journal of Chromatography A, 1995-06, Vol.704 (2), p.369-376

1995

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Fluorous-tethered quenching reagents for solution phase parallel synthesis

Tetrahedron letters, 2002-06, Vol.43 (23), p.4225-4228

2002

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Microwave-initiated living free radical polymerization: rapid formation of custom Rasta resins

Tetrahedron letters, 2003-06, Vol.44 (23), p.4321-4325

2003

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Discovery of N-{[1-(propylsulfonyl)-4-pyridin-2-ylpiperidin-4-yl]methyl}benzami des as novel, selective and potent GlyT1 inhibitors

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (5), p.1488-1491

2009

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Highlights of Applications in Synthesis and Catalysis: 10.6 Fluorous Scavengers

Handbook of Fluorous Chemistry, 2004, p.236-246

2004

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Design, Synthesis, and Tripeptidyl Peptidase II Inhibitory Activity of a Novel Series of ( S )-2,3-Dihydro-2-(4-alkyl-1 H -imidazol-2-yl)-1 H -indoles

Journal of medicinal chemistry, 2002-11, Vol.45 (24), p.5303-5310

2002

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Synthesis of 1,1′‐carbonyldimidazole‐ 1‐ 14 C and its use in preparing a methoxy(polyethylene)glycol semicarbazide linker

Journal of labelled compounds & radiopharmaceuticals, 1995-07, Vol.36 (7), p.661-669

1995

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Fluorous Scavengers

ChemInform, 2005-10, Vol.36 (41), p.no-no

2005

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Synthesis of tritium-labeled azaline B acetate

Journal of labelled compounds & radiopharmaceuticals, 1997-02, Vol.39 (2), p.147-157

1997

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Synthesis of 1,1′-carbonyldimidazole-1-14C and its use in preparing a methoxy(polyethylene)glycol semicarbazide linker

Journal of labelled compounds & radiopharmaceuticals, 1995-07, Vol.36 (7), p.661-669

1995

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Efficient Synthesis of Imidazoles from Aldehydes and 1,2-Diketones Using Microwave Irradiation

Allosteric Akt (PKB) inhibitors: discovery and SAR of isozyme selective inhibitors

General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines

Discovery of 2,3,5-trisubstituted pyridine derivatives as potent Akt1 and Akt2 dual inhibitors

Discovery of N-{[1-(propylsulfonyl)-4-pyridin-2-ylpiperidin-4-yl]methyl}benzamides as novel, selective and potent GlyT1 inhibitors

Design, Synthesis, and In Vivo Efficacy of Glycine Transporter-1 (GlyT1) Inhibitors Derived from a Series of [4-Phenyl-1-(propylsulfonyl)piperidin-4-yl]methyl Benzamides

Structure activity relationships of human galactokinase inhibitors

Discovery of Positive Allosteric Modulators for the Metabotropic Glutamate Receptor Subtype 5 from a Series of N-(1,3-Diphenyl-1H- pyrazol-5-yl)benzamides That Potentiate Receptor Function in Vivo

Fluorous-tethered amine bases for organic and parallel synthesis: scope and limitations

A ‘one pot’ microwave-mediated synthesis of the basic canthine skeleton: expedient access to unnatural β-carboline alkaloids

Discovery of GlyT1 inhibitors with improved pharmacokinetic properties

Synthesis and biological evaluation of unnatural canthine alkaloids

A general Staudinger protocol for solution-phase parallel synthesis

Design, Synthesis, and Tripeptidyl Peptidase II Inhibitory Activity of a Novel Series of (S)-2,3-Dihydro-2-(4-alkyl-1H-imidazol-2-yl)-1H-indoles

Broadening the scope of 1,2,4-triazine synthesis by the application of microwave technology

Analysis and purification of modified methoxy(polyethylene glycol) compounds of similar molecular mass by high-performance liquid chromatography

Fluorous-tethered quenching reagents for solution phase parallel synthesis

Microwave-initiated living free radical polymerization: rapid formation of custom Rasta resins

Discovery of N-{[1-(propylsulfonyl)-4-pyridin-2-ylpiperidin-4-yl]methyl}benzami des as novel, selective and potent GlyT1 inhibitors

Highlights of Applications in Synthesis and Catalysis: 10.6 Fluorous Scavengers

Design, Synthesis, and Tripeptidyl Peptidase II Inhibitory Activity of a Novel Series of ( S )-2,3-Dihydro-2-(4-alkyl-1 H -imidazol-2-yl)-1 H -indoles

Synthesis of 1,1′‐carbonyldimidazole‐ 1‐ 14 C and its use in preparing a methoxy(polyethylene)glycol semicarbazide linker

Fluorous Scavengers

Synthesis of tritium-labeled azaline B acetate

Synthesis of 1,1′-carbonyldimidazole-1-14C and its use in preparing a methoxy(polyethylene)glycol semicarbazide linker

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