INTRODUCTIONThe classic NMR strategy for determining the structure or stereochemistry of small molecules is by using a combination of nuclear overhauser effect (NOE) and scalar J couplings. dependence, where r is the internuclear distance and can be used to connect protons up to 5Å apart. 2 1 H-1 H NOEs have the most utility in small-molecule studies. H-X NOEs usually require isotopic labeling, which can be difficult synthetically for small molecules.1 H-1 H scalar couplings are easy to measure and have high information content; 3 J HH leads to the relative orientations of the atoms by sequential connectivity and estimation of dihedral angles through the well-known Karplus equation.3 Long-range heteronuclear J couplings ( >2 J XH ) are also useful for structural determinations but the data are more difficult to obtain. Typically, these involve 13 C or 15 N as the X-nucleus and if the sample is not isotopically enriched the experiment, such as heteronuclear multiple bond coherence spectroscopy (HMBC), 4,5 can be very time consuming. If the molecule of interest has an overall dearth of protons, has NOEs that cannot be assigned unambiguously or has breaks in the NOE or scalar connectivities, the typical NOE/J analysis fails. Additionally, in order to obtain the relative orientation of remote centers, multiple NOE or J-coupling connections have to be performed in series to transverse the entire molecule. The further away the stereocenters are from each other, the greater the number of necessary connections and measurements needed to confirm unambiguously the connectivity. If one of the connections fails, the pathway fails. Thus, a method that does not rely upon these connectivities would be extremely useful for stereochemistry