Search Results - "Yang, Bryant H"
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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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Journal Article -
2
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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Journal Article -
3
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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Journal Article -
4
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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5
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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6
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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Book Review Journal Article -
7
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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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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9
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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10
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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11
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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12
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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Journal Article -
13
Use of pseudoephedrine as a practical chiral auxiliary for asymmetric synthesis
Published 01-01-1997“…The use of pseudoephedrine as a practical chiral auxiliary for asymmetric synthesis is described. Both enantiomers of pseudoephedrine are inexpensive commodity…”
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Dissertation