Direct Structural Comparison of a Rigid Cyclic Peptidic Scaffold Using Crystallography and NMR in Strained PH Polymer Gels Academic Article uri icon

abstract

  • A small series of biaryl ether containing cyclic peptidic scaffolds was synthesized and cyclized by an S N Ar reaction. The structure of one rigid scaffold was solved by X-ray crystallography and also determined in solution by NMR spectroscopy. Molecular alignment of the peptidic scaffold in strained PH polymer gels in [D 6 ]DMSO was applied to extract residual dipolar couplings (RDCs). The RDC values were used to obtain a structure that was compared to the crystal structure. Good correlation was obtained, indicating that the RDC method represents a very precise structure determination method for small organic molecules in solution.

publication date

  • January 1, 2010