DETERMINATION OF THE STEREOCHEMISTRY OF SUBSTITUTED 4-(SULFOAMIDOALKYL AND SULFONAMIDOALKYL)PIPERIDINE-2-CARBOXYLIC ACIDS WITH H-1-NMR, COSY, AND HOMONUCLEAR NOE EXPERIMENTS
A. Elhadri et al., DETERMINATION OF THE STEREOCHEMISTRY OF SUBSTITUTED 4-(SULFOAMIDOALKYL AND SULFONAMIDOALKYL)PIPERIDINE-2-CARBOXYLIC ACIDS WITH H-1-NMR, COSY, AND HOMONUCLEAR NOE EXPERIMENTS, Spectroscopy letters, 28(5), 1995, pp. 795-803
Basically the aim of this work is to define the accurate configuration
of 4-substituted (sulfo- and sulfonamidoalkyl) piperidine-2-carboxyli
c acids which have been conceived as potential NMDA antagonists. H-1 N
MR and 2D NMR (COSY) followed by qualitative Homonuclear NOE have led
to the assignement of the (+/-) cis and (+/-) trans configuration of t
he whole family's compounds.