Abstract

The conformations of 2- C:1- N-carbonyl-2-deoxyglycopyranosylamines (β-lactams) with the α- d- gluco, α- d- galacto, β- d- arabino, α- l- xylo, α- l- gluco, and β- d- altro configurations have been investigated by X-ray crystallography and n.m.r. spectroscopy. The n.m.r. data, interpreted in terms of an equilibrium of two rapidly interconverting half-chair forms, were supported strongly by the diffractometric data which showed almost regular half-chair conformations.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call