作者:Francisco Camps、Jose Coll、Gemma Fabrias、Angel Guerrero
DOI:10.1016/s0040-4020(01)91296-7
日期:1984.1
Synthesis of fluorinated analogs of some dienic insect sex pherormones through a stereocontrolled Wittig reaction of β-fluorinated aldehydes with the appropriate ω-functionalized ylides is reported. Some features of the 1H and 19F NMR spectra of these analogs are also discussed.
据报道,通过β-氟化醛与适当的ω-官能化的乙炔的立体控制的Wittig反应,合成了一些二齿昆虫性信息素的氟化类似物。还讨论了这些类似物的1 H和19 F NMR光谱的某些特征。