Donald Bankston

A Scaleable Synthesis of BAY 43-9006:  A Potent Raf Kinase Inhibitor for the Treatment of Cancer

Donald Bankston, Jacques Dumas, Reina Natero et al. · Organic Process Research & Development · 2002 · 111 citations

Other Urea Targets, Medicinal Chemistry, Bioorganic Chemistry +15

2-Acetylpyridine thiocarbonohydrazones. Potent inactivators of herpes simplex virus ribonucleotide reductase

Todd A. Blumenkopf, Joan A. Harrington, Cecilia S. Koble et al. · Journal of Medicinal Chemistry · 1992 · 62 citations

Omega-carboxypyridyl substituted ureas as Raf kinase inhibitors

Uday R. Khire, Donald Bankston, J A Barbosa et al. · Bioorganic & Medicinal Chemistry Letters · 2003 · 44 citations · Full text

Molecular Pharmacology, Biochemistry, Medicine +5

Convergent catalytic asymmetric synthesis of camptothecin analog GI147211C

Francis G. Fang, Donald Bankston, Edward M. Huie et al. · Tetrahedron · 1997 · 38 citations

Medicinal Chemistry, Camptothecin Analog Gi147211c, Biochemistry +2

Palladium(II) Acetate−Tris(triphenylphosphine)rhodium(I) Chloride:  A Novel Catalytic Couple for the Intramolecular Heck Reaction

Donald Bankston, Frank Fang, Edward M. Huie et al. · The Journal of Organic Chemistry · 1999 · 35 citations

Inorganic Chemistry, Chemical Engineering, Cross-coupling Reaction +14