Stereoselective and versatile approach for the synthesis of gossyplure and its components
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[1] R. Silverstein. Pheromones: Background and Potential for Use in Insect Pest Control , 1981, Science.
[2] M. Venuti,et al. CYCLIC PHOSPHONIUM YLIDES. A SHORT SYNTHESIS OF GOSSYPLURE , 1981 .
[3] R. G. Salomon,et al. Aleuritic acid, an abundant source of prostanoid synthons , 1978 .
[4] M. Miyashita,et al. Pyridinium p-toluenesulfonate. A mild and efficient catalyst for the tetrahydropyranylation of alcohols , 1977 .
[5] G. Ohloff,et al. Stereoselective Syntheses of the Isomeric 5, 10‐Pentadecadienals , 1977 .
[6] L. A. Bariola,et al. Pink Bollworm: Trap Tests with Gossyplure , 1976 .
[7] C. Henrick,et al. Stereochemical control in Wittig olefin synthesis. Preparation of the pink bollworm sex pheromone mixture, gossyplure , 1975 .
[8] H. Su,et al. Synthesis of the sex pheromone of the female Angoumois grain moth and its geometric isomers. , 1974, Journal of economic entomology.
[9] R. Staten,et al. The pink bollworm sex attractant. , 1974, Journal of economic entomology.
[10] R. Silverstein,et al. Clarification of the Chemical Status of the Pink Bollworm Sex Pheromone , 1973, Science.
[11] R. Ratcliffe,et al. Improved procedure for oxidations with the chromium trioxide-pyridine complex , 1970 .
[12] M. Schlosser,et al. Zwischenstufen der Wittig-Reaktion mit nicht stabilisierten Phosphoryliden , 1964 .
[13] E. Degering,et al. Studies on the Synthesis of Lysine1 , 1950 .