NMR study of the spatial structure of synthetic pyrethroids

The spatial isomers of the new synthetic analogs of ethyl permithrinic ether and permethrin were investigated by NMR (1H, 13C, DEPT (distortionless enhancement by polarization transfer), COSY (correlation spectroscopy), CHCORR (heteronuclear (C, H) shift correlation spectroscopy), ROESY (rotating-frame Overhauser effect spectroscopy)). Several tendencies were revealed in the 1H and 13C chemical shifts of the α atoms of the substituents in the 2nd and 3rd positions of the cyclopropane ring. For substituents cis-orientated relative to the ester group, the spectra show a paramagnetic shift of the 1H signals and the diamagnetic shift of the 13C signals relative to the trans-orientated substituents. The 1H and 13C chemical shifts of the α atoms of the substituents in the 2nd and 3rd positions of the cyclopropane ring permit an unambiguous determination of the stereochemistry of ethyl permethrinic ether and permethrin analogs.