An efficient and stereoselective synthesis of insect pheromones by way of nickel-catalyzed Grignard reactions. Syntheses of gossyplure and pheromones of Eudia pavonia and Droxophila melanogaster.☆
暂无分享,去创建一个
P. Ménez | N. Kunesch | E. Wenkert | G. Kunesch | J. Ducoux
[1] P. Kocieňski,et al. A highly stereoselective and iterative approach to isoprenoid chains: synthesis of homogeraniol, homofarnesol, and homogeranylgeraniol , 1989 .
[2] P. Kocieňski,et al. A stereoselective synthesis of tri-substituted alkenes. The nickel-catalysed coupling of Grignard reagents with 6-alkyl-3,4-dihydro-2H-pyrans , 1988 .
[3] D. Curran,et al. Atom transfer cycloaddition. A facile preparation of functionalized (methylene)cyclopentanes , 1987 .
[4] D. Curran,et al. Atom transfer cyclization reactions of α-iodo carbonyls , 1987 .
[5] V. Ferreira,et al. Synthesis of acyclic, cis olefinic pheromones by way of nickel-catalyzed Grignard reactions , 1985 .
[6] E. Michelotti,et al. Transformation of carbon-oxygen into carbon-carbon bonds mediated by low-valent nickel species , 1984 .
[7] N. N. Joshi,et al. Stereoselective and versatile approach for the synthesis of gossyplure and its components , 1984 .
[8] R. Rossi,et al. Insect pheromone components: Use of 13C NMR spectroscopy for assigning the configuration of CC double bonds of monoenic or dienic pheromone components and for quantitative determination of Z/E mixtures , 1982 .
[9] A. Beckwith. Regio-selectivity and stereo-selectivity in radical reactions , 1981 .
[10] E. Michelotti,et al. Nickel-induced conversion of carbon-oxygen into carbon-carbon bonds. One-step transformations of enol ethers into olefins and aryl ethers into biaryls , 1979 .
[11] G. Ohloff,et al. Stereoselective Syntheses of the Isomeric 5, 10‐Pentadecadienals , 1977 .
[12] K. Eiter,et al. Trennung und analytische bestimmung synthetischer pheromone am beispiel der isomeren 7,11-hexadecadien-1-ylacetate (gossyplure) , 1976 .
[13] C. Henrick,et al. Stereochemical control in Wittig olefin synthesis. Preparation of the pink bollworm sex pheromone mixture, gossyplure , 1975 .
[14] K. Mori,et al. STEREOSELECTIVE SYNTHESIS OF THE PINK BOLLWORM SEX PHEROMONE, (Z,Z)-7,11-HEXADECADIENYL ACETATE AND ITS (Z,E)-ISOMER , 1975 .
[15] P. Sonnet. Practical synthesis of the sex pheromone of the pink bollworm , 1974 .
[16] H. Su,et al. Synthesis of the sex pheromone of the female Angoumois grain moth and its geometric isomers. , 1974, Journal of economic entomology.
[17] R. Silverstein,et al. Clarification of the Chemical Status of the Pink Bollworm Sex Pheromone , 1973, Science.
[18] G. R. Hecke,et al. Ditertiary Phosphine Complexes of Nickel. SpeCtral, Magnetic, and Proton Resonance Studies. A Planar-Tetrahedral Equilibrium , 1966 .