A. Chucholowski

发表

Synthesis and structure-activity relationships of a novel series of non-peptide angiotensin II receptor binding inhibitors specific for the AT2 subtype.

C. J. Blankley, J. C. Hodges, J. Quin, 1991, Journal of medicinal chemistry.

Design and synthesis of 5-aryl-pyridone-carboxamides as inhibitors of anaplastic lymphoma kinase.

Rongshi Li, Jian Wang, Rongshi Li, 2006, Journal of medicinal chemistry.

Stereospecific 1,2-migrations in carbohydrates. Stereocontrolled synthesis of .alpha.- and .beta.-2-deoxyglycosides.

K. Nicolaou, T. Ladduwahetty, J. Randall, 1986, Journal of the American Chemical Society.

Stereospecific 1,2-Migrations in Carbohydrates. Stereocontrolled Synthesis of α- and β-2-Deoxyglycosides.

K. Nicolaou, T. Ladduwahetty, J. Randall, 1986 .

Heterocyclic ureas: inhibitors of acyl-CoA:cholesterol O-acyltransferase as hypocholesterolemic agents.

C. J. Blankley, M. Wilson, R. Stanfield, 1996, Journal of medicinal chemistry.

Reactions of glycosyl fluorides. Synthesis of O-, S-, and N-glycosides

K. Nicolaou, J. Randall, A. Chucholowski, 1984 .

Reactions of glycosyl fluorides. Synthesis of C-glycosides

K. Nicolaou, R. Dolle, J. Randall, 1984 .

Inhibitors of cholesterol biosynthesis. 3. Tetrahydro-4-hydroxy-6-[2-(1H-pyrrol-1-yl)ethyl]-2H-pyran-2-one inhibitors of HMG-CoA reductase. 2. Effects of introducing substituents at positions three and four of the pyrrole nucleus.

C J Blankley, C. J. Blankley, D. Ortwine, 1991, Journal of medicinal chemistry.

Heterobiaryl human immunodeficiency virus entry inhibitors.

D. Bolognesi, S. Fisher, M. Greenberg, 2009, Journal of medicinal chemistry.

threo-3-Hydroxycarboxylic acids as key intermediates in a highly stereoselective synthesis of (Z)- and (E)-olefins and enol ethers

Andreas Pointner, A. Pointner, J. Mulzer, 1979 .

Novel Solution‐ and Solid‐Phase Strategies for the Parallel and Combinatorial Synthesis of Small‐Molecular‐Weight Compound Libraries

D. Obrecht, T. Masquelin, J. M. Villalgordo, 1997 .

Stereoselective additions to carboxylic acid dianions and β-lactone substituted ester enolates

J. Mulzer, G. Huttner, I. Jibril, 1984 .

Diastereoselective Michael additions of β-lactone enolates to dimethyl maleate

J. Mulzer, G. Huttner, I. Jibril, 1983 .

Competition in the Three‐Component System Triphenylphosphane/Azo Ester/3‐Hydroxy‐Carboxylic Acid: OH ? versus COOH‐Activation

J. Mulzer, A. Chucholowski, Gisela Brüntrup, 1979 .

Base catalyzed rearrangement of 5-cyanomethyl-2-isoxazolines; novel pathway for the formation of 2-aminopyridine N-oxides

A. Chucholowski, S. Uhlendorf, 1990 .

Three‐Center Diastereoselective Aldol Additions of β‐Lactone Enolates to Aldehydes

J. Mulzer, A. Chucholowski, 1982 .

Relationship between tissue selectivity and lipophilicity for inhibitors of HMG-CoA reductase.

C. J. Blankley, B. Roth, T. Bocan, 1991, Journal of medicinal chemistry.

Oxidosqualene cyclase (OSC) inhibitors for the treatment of dyslipidemia

T. Schulz-Gasch, M. Kansy, R. Thoma, 2005 .

Design and Synthesis of Human Immunodeficiency Virus Entry Inhibitors: Sulfonamide as an Isostere for the α-Ketoamide Group

Rongshi Li, D. Bolognesi, S. Fisher, 2007 .