Conformational analysis by carbon-13 nuclear magnetic resonance spectroscopy. Part I. Hexahydro-3H-oxazolo[3,4-a] pyridines

Abstract
Compraison of the C(3), C(1), and C(8a) chemical shifts in hexahydro-3H-oxazolo [3,4-a] pyridine with those in methyl substituted derivatives suggests its existence in solution at n.m.r. probe temperature as a cistrans equilibrium mixture containing 73–78% of the trans-fused conformation; 13C–H coupling constants involving the C(3) protons are dependent upon the orientation of adjacent heteroatom lone pairs.

This publication has 0 references indexed in Scilit: