Daniel A. Ruppar

Highly selective enantiomer differentiation in intramolecular cyclopropanation reactions of racemic secondary allylic diazoacetates.

Michael P. Doyle, Alexey B. Dyatkin, Daniel A. Ruppar et al. · Journal of the American Chemical Society · 1995 · 91 citations

Molecular Sciences, Engineering, Biochemistry +15

Enhancement of enantiocontrol/diastereocontrol in catalytic intramolecular cyclopropanation and carbon-hydrogen insertion reactions of diazoacetates with Rh2(4S-MPPIM)4

Michael P. Doyle, Qi‐Lin Zhou, Alexey B. Dyatkin et al. · Tetrahedron Letters · 1995 · 80 citations

Novel Organocatalysts, Engineering, Carbon-hydrogen Insertion Reactions +9

Structure–activity relationships and sub-type selectivity in an oxabicyclic estrogen receptor α/β agonist scaffold

Lawrence G. Hamann, Jeffrey H. Meyer, Daniel A. Ruppar et al. · Bioorganic & Medicinal Chemistry Letters · 2005 · 39 citations · Full text

Molecular Pharmacology, Biochemistry, Sub-type Selectivity +9

Effects of isosteric pyridone replacements in androgen receptor antagonists based on 1,2-dihydro- and 1,2,3,4-tetrahydro-2,2-dimethyl-6-trifluoromethyl-8-pyridono[5,6-g]quinolines

James W. Kong, Lawrence G. Hamann, Daniel A. Ruppar et al. · Bioorganic & Medicinal Chemistry Letters · 2000 · 15 citations · Full text

Androgen Receptor Antagonists, Medicinal Chemistry, Medicine +8