Stereoselective synthesis of optically active disparlure, the pheromone of the gypsy moth (Porthetria dispar L.)

Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters

James A. Dale, Harry S. Mosher · Journal of the American Chemical Society · 1973 · 2.6K citations

Natural Sciences, Chemistry, Nuclear Chemistry +6

Potent Sex Attractant of the Gypsy Moth: Its Isolation, Identification, and Synthesis

B. A. Bierl, Morton Beroza, C. W. Collier · Science · 1970 · 292 citations

Life Sciences, Chemistry, Entomology +15

Synthesis and activity of optically active disparlure

Shigeru Iwaki, Shingo Marumo, Tetsuo Saito et al. · Journal of the American Chemical Society · 1974 · 147 citations

Natural Sciences, Chemistry, Analytical Chemistry +4

Reactions of lithium diorganocuprates(I) with tosylates. I. Synthetic aspects

Carl R. Johnson, Gerard A. Dutra · Journal of the American Chemical Society · 1973 · 136 citations

Natural Sciences, Chemistry, Chemical Kinetics +5

Synthesis of exo-brevicomin, the pheromone of western pine beetle, to obtain optically active forms of known absolute configuration

Kenji Mori · Tetrahedron · 1974 · 92 citations

Life Sciences, Entomology, Forest Entomology +10