Synthesis of optically active forms of methyl (E)-2,4,5-tetradecatrienoate, the pheromone of the male dried bean beetle

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

Chemical Analysis, Magnetic Resonance, Altmetric Attention Score +16

Modern organoselenium chemistry

Derrick L. J. Clive · Tetrahedron · 1978 · 473 citations

Organic Chemistry, Modern Organoselenium Chemistry, Main Group Chemistry +1

Stereo- and regiochemistry of the Claisen rearrangement: applications to natural products synthesis

Frederick E. Ziegler · Accounts of Chemical Research · 1977 · 254 citations

Altmetrics, Natural Products Synthesis, Engineering +15

Pheromone synthesis. 4. A synthesis of (.+-.)-methyl n-tetradeca-trans-2,4,5-trienoate, an allenic ester produced by the male dried bean beetle Acanthoscelides obtectus (Say)

Philip Kocieński, George Cernigliaro, G. Feldstein · The Journal of Organic Chemistry · 1977 · 100 citations

Bioorganic Chemistry, Engineering, Entomology +17

ENANTIOSELECTIVE ADDITION OF ACETYLENE TO ALDEHYDE. PREPARATION OF OPTICALLY ACTIVE ALKYNYL ALCOHOLS

Teruaki Mukaiyama, Keisuke Suzuki, Kenso Soai et al. · Chemistry Letters · 1979 · 70 citations

Enantioselective Synthesis, Derivatives, Engineering +11