The configuration and conformations of stereoisomeric 4R-8-(3,4-dihydro-2-pyranyloxy)quinolines were studied by means of their PMR spectra. It was established that the trans isomers of the investigated compounds have primarily a "half-chair" conformation and display an anomeric effect. A "sofa" conformation is proposed for the labile cis isomers.
|Number of pages||4|
|Journal||Chemistry of Heterocyclic Compounds|
|State||Published - 1 May 1976|
ASJC Scopus subject areas
- Organic Chemistry