Search Results - "Yang, Bryant"
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Half-life extension of peptidic APJ agonists by N-terminal lipid conjugation
Published in Bioorganic & medicinal chemistry letters (01-11-2020)“…[Display omitted] •Lipidated apelin-13 showed in an increase in ejection fraction in an anesthetized rat myocardial infarction model.•Rat plasma protein…”
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2
Highly Active Palladium Catalysts for Suzuki Coupling Reactions
Published in Journal of the American Chemical Society (20-10-1999)“…Mixtures of palladium acetate and o-(di-tert-butylphosphino)biphenyl (4) catalyze the room-temperature Suzuki coupling of aryl bromides and aryl chlorides with…”
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3
Palladium-catalyzed amination of aryl halides and sulfonates
Published in Journal of Organometallic Chemistry (15-03-1999)“…In this review, the progress made in the palladium-catalyzed amination of aryl halides and sulfonates is described with particular attention given to…”
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4
Design and Preparation of a Potent Series of Hydroxyethylamine Containing β-Secretase Inhibitors That Demonstrate Robust Reduction of Central β-Amyloid
Published in Journal of medicinal chemistry (08-11-2012)“…A series of potent hydroxyethyl amine (HEA) derived inhibitors of β-site APP cleaving enzyme (BACE1) was optimized to address suboptimal pharmacokinetics and…”
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5
Bacterial coinfections with coronavirus disease 2019 (COVID-19)
Published in Antimicrobial stewardship & healthcare epidemiology : ASHE (01-01-2021)“…Abstract Background: The pandemic caused by severe acute respiratory coronavirus virus 2 (SARS-CoV-2) has dramatically increased cheshospitalizations, and it…”
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6
A Palladium-Catalyzed Method for the Preparation of Indoles via the Fischer Indole Synthesis
Published in Journal of the American Chemical Society (10-11-1999)“…A Pd-catalyzed method for the preparation of N-aryl benzophenone hydrazones 4 is described. The use of a Pd/BINAP-based catalyst provides hydrazones 4 in good…”
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7
Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones
Published in Journal of the American Chemical Society (16-07-1997)“…The use of pseudoephedrine as a practical chiral auxiliary for asymmetric synthesis is described in full. Both enantiomers of pseudoephedrine are inexpensive…”
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8
The Development of Efficient Protocols for the Palladium-Catalyzed Cyclization Reactions of Secondary Amides and Carbamates
Published in Organic letters (15-07-1999)“…With the proper choice of palladium catalyst, ligand, and base, five-, six-, and seven-membered rings are formed efficiently from secondary amide or secondary…”
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9
Design and Synthesis of Potent, Orally Efficacious Hydroxyethylamine Derived β-Site Amyloid Precursor Protein Cleaving Enzyme (BACE1) Inhibitors
Published in Journal of medicinal chemistry (08-11-2012)“…We have previously shown that hydroxyethylamines can be potent inhibitors of the BACE1 enzyme and that the generation of BACE1 inhibitors with CYP 3A4…”
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10
Hydroxyethylamine-based inhibitors of BACE1: P1–P3 macrocyclization can improve potency, selectivity, and cell activity
Published in Bioorganic & medicinal chemistry letters (01-08-2013)“…We describe a systematic study of how macrocyclization in the P1–P3 region of hydroxyethylamine-based inhibitors of β-site amyloid precursor protein…”
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11
A Palladium-Catalyzed Strategy for the Preparation of Indoles: A Novel Entry into the Fischer Indole Synthesis
Published in Journal of the American Chemical Society (08-07-1998)Get full text
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12
Use of Pseudoephedrine as a Practical Chiral Auxiliary for Asymmetric Synthesis
Published in Journal of the American Chemical Society (01-10-1994)Get full text
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13
Clinical Characteristics and Outcomes of Coronavirus Disease 2019 Patients Who Received Compassionate-Use Leronlimab
Published in Clinical infectious diseases (06-12-2021)“…Abstract Background Leronlimab, a monoclonal antibody blocker of C-C chemokine receptor type 5 originally developed to treat human immunodeficiency virus…”
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14
Lithium amidotrihydroborate, a powerful new reductant. Transformation of tertiary amides to primary alcohols
Published in Tetrahedron letters (01-05-1996)“…Lithium amidotrihydroborate (LiH 2NBH 3, LAB) is a new and highly nucleophilic reducing agent that is easily prepared by deprotonation of the commerical…”
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657. Diagnostic Utility of Dedicated Fungal Blood Cultures for Diagnosis of Candidemia
Published in Open forum infectious diseases (31-12-2020)“…Abstract Background Blood culture techniques have improved to the point where they are considered sensitive enough for detection of Candida. Expert guidelines…”
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Abstract 19511: Progesterone Reduces Isoproterenol-Induced pVTs in Male Transgenic Long QT Syndrome 2 (LQT2) Rabbits
Published in Circulation (New York, N.Y.) (20-11-2012)“…Abstract only Background: During childhood, boys with long QT syndrome (LQT) have a higher risk than girls for developing ventricular arrhythmia and sudden…”
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Hydroxyethylamine-based inhibitors of BACE1: P1aP3 macrocyclization can improve potency, selectivity, and cell activity
Published in Bioorganic & medicinal chemistry letters (01-08-2013)“…We describe a systematic study of how macrocyclization in the P1aP3 region of hydroxyethylamine-based inhibitors of I2-site amyloid precursor protein…”
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18
Abstract 349: Functional Scaffold-Free 3D Cardiac Microtissues: A Novel Model for the Investigation of Heart Cells
Published in Circulation research (03-08-2012)“…Abstract only To bridge the gap between 2D cell culture and tissue, various 3D cell culture approaches have been developed for the investigation of cardiac…”
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A Potent and Orally Efficacious, Hydroxyethylamine-Based Inhibitor of β-Secretase
Published in ACS medicinal chemistry letters (08-11-2012)“…β-Secretase inhibitors are potentially disease-modifying treatments for Alzheimer's disease. Previous efforts in our laboratory have resulted in…”
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Discovery of thienopyridines as Src-family selective Lck inhibitors
Published in Bioorganic & medicinal chemistry letters (01-03-2007)“…We describe the identification, SAR, and in vivo pharmacology of a new series of Src-family selective Lck inhibitors. These thienopyridines were designed to…”
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