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Preparation of (4-Amino-1-Hydroxybutylidene)bisphosphonic Acid Sodium Salt, MK-217 (Alendronate Sodium). An Improved Procedure for the Preparation of 1-Hydroxy-1,1-bisphosphonic Acids

Journal of organic chemistry, 1995-12, Vol.60 (25), p.8310-8312

1995

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Synthesis of the first sulfur-35-labeled hERG radioligand

Bioorganic & medicinal chemistry letters, 2006-03, Vol.16 (6), p.1692-1695

2006

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Practical enantioselective synthesis of a homotyrosine derivative and (R,R)-4-propyl-9-hydroxynaphthoxazine, a potent dopamine agonist

Journal of organic chemistry, 1987-11, Vol.52 (23), p.5143-5150

1987

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Use of fluorous and solid-phase electrophiles as scavengers for excess amine in the preparation of sulfur-35 labelled radioligands

Journal of labelled compounds & radiopharmaceuticals, 2005-03, Vol.48 (3), p.203-208

2005

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Development of a High Specific Activity Sulfur-35-Labeled Sulfonamide Radioligand That Allowed the Identification of a New Growth Hormone Secretagogue Receptor

Journal of medicinal chemistry, 1996-04, Vol.39 (9), p.1767-1770

1996

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Synthesis of [35S]aryl sulfonyl chlorides from [35S]elemental sulfur

Journal of labelled compounds & radiopharmaceuticals, 2005-03, Vol.48 (4), p.275-283

2005

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A convenient method for [14C] carbonylation reactions

Journal of labelled compounds & radiopharmaceuticals, 2000-10, Vol.43 (11), p.1135-1144

2000

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Applications of LC-ARC™ stop-flow radiochemical detection

Journal of labelled compounds & radiopharmaceuticals, 2007-04, Vol.50 (5-6), p.543-544

2007

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Synthesis of two non-peptidyl GnRH receptor antagonists via [14C]carbonylation

Journal of labelled compounds & radiopharmaceuticals, 2003-09, Vol.46 (10), p.993-1000

2003

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Use of Dibutyl[14C]formamide as a Formylating Reagent in the Vilsmeier-Haack Reaction and Synthesis of a 14C-Labeled Novel Phosphodiesterase-4 (PDE-4) Inhibitor

Helvetica chimica acta, 2005-05, Vol.88 (5), p.1040-1047

2005

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A Receptor in Pituitary and Hypothalamus that Functions in Growth Hormone Release

Science (American Association for the Advancement of Science), 1996-08, Vol.273 (5277), p.974-977

1996

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Carbon-14 labeling of a trifluoromethoxy group: synthesis of a substance P antagonist

Journal of labelled compounds & radiopharmaceuticals, 2001-10, Vol.44 (12), p.815-829

2001

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Synthesis of [3,5-dichlorobenzenesulfonamide-U-14C)] labeled VLA-4 antagonists

Journal of labelled compounds & radiopharmaceuticals, 2004-02, Vol.47 (2), p.115-125

2004

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Ultrasonic particle size reduction of radiolabeled pharmaceuticals

Journal of labelled compounds & radiopharmaceuticals, 2004-06, Vol.47 (7), p.399-406

2004

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Synthesis of [C2H3]methotrexate and [C2H3]7-hydroxymethotrexate

Journal of labelled compounds & radiopharmaceuticals, 2002-01, Vol.45 (1), p.29-36

2002

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An enantioselective approach to (+)-thienamycin from dimethyl 1,3-acetonedicarboxylate and (+)-.alpha.-methylbenzylamine

Journal of organic chemistry, 1986-05, Vol.51 (9), p.1498-1504

1986

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Perhydroindan derivatives. XVI. Synthesis of racemic epiallogibberic acid (3)

Journal of organic chemistry, 1973-04, Vol.38 (7), p.1398-1403

1973

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Diastereoselective routes to a 1.beta.-methylcarbapenem key intermediate. Scope of ate complex formation between ester enolates and organoboranes and -alanes

Journal of organic chemistry, 1992-04, Vol.57 (8), p.2411-2418

1992

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Use of Dibutyl[ 14 C]formamide as a Formylating Reagent in the Vilsmeier – Haack Reaction and Synthesis of a 14 C‐Labeled Novel Phosphodiesterase‐4 (PDE‐4) Inhibitor

Helvetica chimica acta, 2005-05, Vol.88 (5), p.1040-1047

2005

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Synthesis of 13C-Labeled Pyrazinone Thrombin Inhibitors and Elucidation of Metabolic Activation Pathways

Helvetica chimica acta, 2004-03, Vol.87 (3), p.674-681

2004

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Synthesis of 13 C‐Labeled Pyrazinone Thrombin Inhibitors and Elucidation of Metabolic Activation Pathways

Helvetica chimica acta, 2004-03, Vol.87 (3), p.674-681

2004

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Efficient utilization of [ 14C]carbon dioxide as a phosgene equivalent for labeled synthesis

Tetrahedron letters, 1997-02, Vol.38 (6), p.919-922

1997

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Cyclization of unsaturated hydroxylamine derivatives

Journal of organic chemistry, 1976-03, Vol.41 (5), p.855-863

1976

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Perhydroindan derivatives. XV. Synthesis of a tetracyclic precursor to epiallogibberic acid

Journal of organic chemistry, 1973-02, Vol.38 (4), p.741-748

1973

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Suzuki cross-coupling for the incorporation of labeled methyl groups onto aryl halides. A synthesis of [14C]tosyl chloride and its use in the synthesis of [14C]L-738,167

Journal of labelled compounds & radiopharmaceuticals, 1999-05, Vol.42 (5), p.469-476

1999

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Preparation of (4-Amino-1-Hydroxybutylidene)bisphosphonic Acid Sodium Salt, MK-217 (Alendronate Sodium). An Improved Procedure for the Preparation of 1-Hydroxy-1,1-bisphosphonic Acids

Synthesis of the first sulfur-35-labeled hERG radioligand

Practical enantioselective synthesis of a homotyrosine derivative and (R,R)-4-propyl-9-hydroxynaphthoxazine, a potent dopamine agonist

Use of fluorous and solid-phase electrophiles as scavengers for excess amine in the preparation of sulfur-35 labelled radioligands

Development of a High Specific Activity Sulfur-35-Labeled Sulfonamide Radioligand That Allowed the Identification of a New Growth Hormone Secretagogue Receptor

Synthesis of [35S]aryl sulfonyl chlorides from [35S]elemental sulfur

A convenient method for [14C] carbonylation reactions

Applications of LC-ARC™ stop-flow radiochemical detection

Synthesis of two non-peptidyl GnRH receptor antagonists via [14C]carbonylation

Use of Dibutyl[14C]formamide as a Formylating Reagent in the Vilsmeier-Haack Reaction and Synthesis of a 14C-Labeled Novel Phosphodiesterase-4 (PDE-4) Inhibitor

A Receptor in Pituitary and Hypothalamus that Functions in Growth Hormone Release

Carbon-14 labeling of a trifluoromethoxy group: synthesis of a substance P antagonist

Synthesis of [3,5-dichlorobenzenesulfonamide-U-14C)] labeled VLA-4 antagonists

Ultrasonic particle size reduction of radiolabeled pharmaceuticals

Synthesis of [C2H3]methotrexate and [C2H3]7-hydroxymethotrexate

An enantioselective approach to (+)-thienamycin from dimethyl 1,3-acetonedicarboxylate and (+)-.alpha.-methylbenzylamine

Perhydroindan derivatives. XVI. Synthesis of racemic epiallogibberic acid (3)

Diastereoselective routes to a 1.beta.-methylcarbapenem key intermediate. Scope of ate complex formation between ester enolates and organoboranes and -alanes

Use of Dibutyl[ 14 C]formamide as a Formylating Reagent in the Vilsmeier – Haack Reaction and Synthesis of a 14 C‐Labeled Novel Phosphodiesterase‐4 (PDE‐4) Inhibitor

Synthesis of 13C-Labeled Pyrazinone Thrombin Inhibitors and Elucidation of Metabolic Activation Pathways

Synthesis of 13 C‐Labeled Pyrazinone Thrombin Inhibitors and Elucidation of Metabolic Activation Pathways

Efficient utilization of [ 14C]carbon dioxide as a phosgene equivalent for labeled synthesis

Cyclization of unsaturated hydroxylamine derivatives

Perhydroindan derivatives. XV. Synthesis of a tetracyclic precursor to epiallogibberic acid

Suzuki cross-coupling for the incorporation of labeled methyl groups onto aryl halides. A synthesis of [14C]tosyl chloride and its use in the synthesis of [14C]L-738,167

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