(E,Z)-2,13-octadecadien-1-ol acetate. A new pheromone structure for sesiid moths

“P-2 nickel” catalyst with ethylenediamine, a novel system for highly stereospecific reduction of alkynes to cis-olefins

Charles A. Brown, V. K. AHUJA · Journal of the Chemical Society Chemical Communications · 1973 · 259 citations

Chemical Engineering, Novel System, Engineering +13

New stereospecific synthesis of trisubstituted olefins. Stereospecific synthesis of farnesol

E. J. Corey, John A. Katzenellenbogen, Gary H. Posner · Journal of the American Chemical Society · 1967 · 237 citations

Engineering, Trisubstituted Olefins, Altmetric Attention Score +9

Saline hydrides and superbases in organic reactions. IX. Acetylene zipper. Exceptionally facile contrathermodynamic multipositional isomeriazation of alkynes with potassium 3-aminopropylamide

Charles A. Brown, Ayako Yamashita · Journal of the American Chemical Society · 1975 · 208 citations

Saline Hydrides, Acetylene Zipper, Cross-coupling Reaction +13

Sex pheromone chemistry of female corn earworm moth,Heliothis zea

Jerome A. Klun, Jack R. Plimmer, B. A. Bierl-Leonhardt et al. · Journal of Chemical Ecology · 1980 · 116 citations

Biology, Pheromone Biochemistry, Entomology +2

Stereoselective synthesis of alkyl (2E,4E)- and (2Z,4E)-3,7,11-trimethyl-2,4-dodecadienoates. Insect growth regulators with juvenile hormone activity

Clive A. Henrick, W. Edward Willy, J.W. Baum et al. · The Journal of Organic Chemistry · 1975 · 57 citations

Natural Product Synthesis, Biochemistry, Natural Sciences +11