Edward D. Robinson

A mild method for the synthesis of furans. Application to 2,5-bridged furano macrocyclic compounds

James A. Marshall, Edward D. Robinson · The Journal of Organic Chemistry · 1990 · 206 citations

Combinatorial Chemistry, Derivative (Chemistry), Molecular Sciences +13

First-in-Class Pan Caspase Inhibitor Developed for the Treatment of Liver Disease

Steven D. Linton, Teresa Aja, Robert A. Armstrong et al. · Journal of Medicinal Chemistry · 2005 · 105 citations

Pathology, Pharmacotherapy, Oxidative Stress +18

Furans in synthesis. 11. Total syntheses of (.+-.)- and (-)-fastigilin C

Steven P. Tanis, Edward D. Robinson, Mark C. McMills et al. · Journal of the American Chemical Society · 1992 · 63 citations

Bioorganic Chemistry, Engineering, Biochemistry +13

[2,3] Wittig rearrangement of nonracemic propargyl ethers leading to allenes of high stereochemical integrity

James A. Marshall, Edward D. Robinson, Antonio Zapata · The Journal of Organic Chemistry · 1989 · 61 citations

Molecular Sciences, Engineering, Alkene Metathesis +14

Synthesis of the tumor-inhibitory tobacco constituents .alpha.- and .beta.-2,7,11-cembratriene-4,6-diol by diastereoselective [2,3] Wittig ring contraction

James A. Marshall, Edward D. Robinson, Jacques Lebreton · The Journal of Organic Chemistry · 1990 · 60 citations

Molecular Pharmacology, Medicinal Chemistry, Pharmaceutical Science +15