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Use of N-Fmoc amino acid chlorides and activated 2-(fluorenylmethoxy)-5(4H)-oxazolones in solid-phase peptide synthesis. Efficient syntheses of highly N-alkylated cyclic hexapeptide oxytocin antagonists related to L-365,209

Journal of organic chemistry, 1992-07, Vol.57 (16), p.4394-4400

1992

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1-(((7,7-Dimethyl-2(S)-(2(S)-amino-4-(methylsulfonyl)butyramido)bicyclo[2.2.1]heptan-1(S)-yl)methyl)sulfonyl)-4-(2-methylphenyl)piperazine (L-368,899): An Orally Bioavailable, Non-Peptide Oxytocin Antagonist with Potential Utility for Managing Preterm Labor

Journal of medicinal chemistry, 1994-03, Vol.37 (5), p.565-571

1994

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Inhibition of steroid 5.alpha.-reductase by unsaturated 3-carboxy steroids

Journal of medicinal chemistry, 1990-03, Vol.33 (3), p.943-950

1990

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Development of a novel class of cyclic hexapeptide oxytocin antagonists based on a natural product

Journal of medicinal chemistry, 1992-10, Vol.35 (21), p.3905-3918

1992

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1-[1-[4-[(N-Acetyl-4-piperidinyl)oxy]-2- methoxybenzoyl]piperidin-4-yl]-4H-3,1- benzoxazin-2(1H)-one (L-371,257): a new, orally bioavailable, non-peptide oxytocin antagonist

Journal of medicinal chemistry, 1995-11, Vol.38 (23), p.4634-4636

1995

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Development of Orally Active Oxytocin Antagonists: Studies on 1-(1-{4-[1-(2-Methyl-1-oxidopyridin-3-ylmethyl)piperidin-4-yloxy]-2- methoxybenzoyl}piperidin-4-yl)-1,4-dihydrobenz[d][1,3]oxazin-2-one (L-372,662) and Related Pyridines

Journal of medicinal chemistry, 1998-06, Vol.41 (12), p.2146-2163

1998

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Steroidal A ring aryl carboxylic acids: a new class of steroid 5.alpha.-reductase inhibitors

Journal of medicinal chemistry, 1990-03, Vol.33 (3), p.937-942

1990

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1-{1-[4-[(N-acetyl-4-piperidinyl)oxy]-2-methoxybenzoyl]piperidin-4-yl}-4H-3,1-benzoxazin-2(1H)-one (L-371,257) : a new, orally bioavailable, non-peptide oxytocin antagonist

Journal of medicinal chemistry, 1995-11, Vol.38 (23), p.4634-4636

1995

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Palladium-catalyzed phosphorylation of alkenyl triflates

Tetrahedron letters, 1989, Vol.30 (40), p.5393-5396

1989

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Inhibition of steroid 5α-reductase by unsaturated 3-carboxysteroids

Journal of medicinal chemistry, 1990-03, Vol.33 (3), p.943-950

1990

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Steroidal a ring aryl carboxylic acids : a new class of steroid 5α-reductase inhibitors

Journal of medicinal chemistry, 1990-03, Vol.33 (3), p.937-942

1990

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Design and synthesis of N-alkylated saccharins as selective α-1a adrenergic receptor antagonists

Bioorganic & medicinal chemistry letters, 1998-09, Vol.8 (18), p.2467-2472

1998

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4-Oxospiro[benzopyran-2,4′-piperidines] as selective α1a-adrenergic receptor antagonists

Bioorganic & medicinal chemistry letters, 1999, Vol.9 (2), p.291-294

1999

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Nanomolar-affinity, non-peptide oxytocin receptor antagonists

Journal of medicinal chemistry, 1993-12, Vol.36 (25), p.3993-4005

1993

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Conformationally constrained o-tolylpiperazine camphorsulfonamide oxytocin antagonists. Structural modifications that provide high receptor affinity and suggest a bioactive conformation

Bioorganic & medicinal chemistry, 1994-09, Vol.2 (9), p.971-985

1994

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Potent inhibition of human steroid 5α-reductase (EC 1.3.1.30) by 3-androstene-3-carboxylic acids

Bioorganic chemistry, 1989-09, Vol.17 (3), p.372-376

1989

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3-Phosphinic acid and 3-phosphonic acid steroids as inhibitors of steroid 5α-reductase: Species comparison and mechanistic studies

Bioorganic chemistry, 1991-09, Vol.19 (3), p.245-260

1991

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ChemInform Abstract: 4-Oxospiro[benzopyran-2,4′-piperidines] as Selective α1a-Adrenergic Receptor Antagonists

ChemInform, 1999-05, Vol.30 (20), p.no-no

1999

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ChemInform Abstract: 4‐Oxospiro[benzopyran‐2,4′‐piperidines] as Selective α 1a ‐Adrenergic Receptor Antagonists

ChemInform, 1999-05, Vol.30 (20)

1999

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The systemic inflammatory response to Clostridium difficile infection

PloS one, 2014-03, Vol.9 (3), p.e92578-e92578

2014

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Combined semi-empirical screening and design of experiments (DOE) approach to identify candidate formulations of a lyophilized live attenuated tetravalent viral vaccine candidate

Vaccine, 2018-05, Vol.36 (22), p.3169-3179

2018

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Climate change decreases the cooling effect from postfire albedo in boreal North America

Global change biology, 2020-03, Vol.26 (3), p.1592-1607

2020

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Evaluation of Cost, Payments, Healthcare Utilization, and Perioperative and Post-Operative Outcomes of Patients Treated with Posterior Lumbar Spinal Surgery Using Open versus Minimally Invasive Surgical Approaches

Medical devices (Auckland, N.Z.), 2021-01, Vol.14, p.173-183

2021

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ACC/AHA/ASE/ASNC/HRS/IAC/Mended Hearts/NASCI/RSNA/SAIP/SCAI/SCCT/SCMR/SNMMI 2014 Health Policy Statement on Use of Noninvasive Cardiovascular Imaging

Journal of the American College of Cardiology, 2014-02, Vol.63 (7), p.698-721

2014

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A survey of the global impact of COVID‐19 on the practice of pediatric anesthesia: A study from the pediatric anesthesia COVID‐19 Collaborative Group

Pediatric anesthesia, 2021-06, Vol.31 (6), p.720-729

2021

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Use of N-Fmoc amino acid chlorides and activated 2-(fluorenylmethoxy)-5(4H)-oxazolones in solid-phase peptide synthesis. Efficient syntheses of highly N-alkylated cyclic hexapeptide oxytocin antagonists related to L-365,209

1-(((7,7-Dimethyl-2(S)-(2(S)-amino-4-(methylsulfonyl)butyramido)bicyclo[2.2.1]heptan-1(S)-yl)methyl)sulfonyl)-4-(2-methylphenyl)piperazine (L-368,899): An Orally Bioavailable, Non-Peptide Oxytocin Antagonist with Potential Utility for Managing Preterm Labor

Inhibition of steroid 5.alpha.-reductase by unsaturated 3-carboxy steroids

Development of a novel class of cyclic hexapeptide oxytocin antagonists based on a natural product

1-[1-[4-[(N-Acetyl-4-piperidinyl)oxy]-2- methoxybenzoyl]piperidin-4-yl]-4H-3,1- benzoxazin-2(1H)-one (L-371,257): a new, orally bioavailable, non-peptide oxytocin antagonist

Development of Orally Active Oxytocin Antagonists: Studies on 1-(1-{4-[1-(2-Methyl-1-oxidopyridin-3-ylmethyl)piperidin-4-yloxy]-2- methoxybenzoyl}piperidin-4-yl)-1,4-dihydrobenz[d][1,3]oxazin-2-one (L-372,662) and Related Pyridines

Steroidal A ring aryl carboxylic acids: a new class of steroid 5.alpha.-reductase inhibitors

1-{1-[4-[(N-acetyl-4-piperidinyl)oxy]-2-methoxybenzoyl]piperidin-4-yl}-4H-3,1-benzoxazin-2(1H)-one (L-371,257) : a new, orally bioavailable, non-peptide oxytocin antagonist

Palladium-catalyzed phosphorylation of alkenyl triflates

Inhibition of steroid 5α-reductase by unsaturated 3-carboxysteroids

Steroidal a ring aryl carboxylic acids : a new class of steroid 5α-reductase inhibitors

Design and synthesis of N-alkylated saccharins as selective α-1a adrenergic receptor antagonists

4-Oxospiro[benzopyran-2,4′-piperidines] as selective α1a-adrenergic receptor antagonists

Nanomolar-affinity, non-peptide oxytocin receptor antagonists

Conformationally constrained o-tolylpiperazine camphorsulfonamide oxytocin antagonists. Structural modifications that provide high receptor affinity and suggest a bioactive conformation

Potent inhibition of human steroid 5α-reductase (EC 1.3.1.30) by 3-androstene-3-carboxylic acids

3-Phosphinic acid and 3-phosphonic acid steroids as inhibitors of steroid 5α-reductase: Species comparison and mechanistic studies

ChemInform Abstract: 4-Oxospiro[benzopyran-2,4′-piperidines] as Selective α1a-Adrenergic Receptor Antagonists

ChemInform Abstract: 4‐Oxospiro[benzopyran‐2,4′‐piperidines] as Selective α 1a ‐Adrenergic Receptor Antagonists

The systemic inflammatory response to Clostridium difficile infection

Combined semi-empirical screening and design of experiments (DOE) approach to identify candidate formulations of a lyophilized live attenuated tetravalent viral vaccine candidate

Climate change decreases the cooling effect from postfire albedo in boreal North America

Evaluation of Cost, Payments, Healthcare Utilization, and Perioperative and Post-Operative Outcomes of Patients Treated with Posterior Lumbar Spinal Surgery Using Open versus Minimally Invasive Surgical Approaches

ACC/AHA/ASE/ASNC/HRS/IAC/Mended Hearts/NASCI/RSNA/SAIP/SCAI/SCCT/SCMR/SNMMI 2014 Health Policy Statement on Use of Noninvasive Cardiovascular Imaging

A survey of the global impact of COVID‐19 on the practice of pediatric anesthesia: A study from the pediatric anesthesia COVID‐19 Collaborative Group

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