Abstract: An important development in the field of NMR has been the advent of hyperpolarization approaches, capable of yielding nuclear spin states whose order exceeds by orders-of-magnitude what even the highest-field spectrometers can afford under Boltzmann equilibrium. Included among these methods is an ex-situ dynamic nuclear polarization (DNP) approach, yielding liquid-phase samples possessing spin polarizations in the 10s of percent. Although capable of providing an NMR sensitivity equivalent to the averaging of ca. 1,000,000 scans, this methodology is constrained to extract its "super-spectrum" within a single -or at most a few- transients. This makes it a poor starting point for conventional 2D NMR acquisition experiments, requiring a large number of scans that are identical to one another except for the incrementation of a certain t1 delay. It has been recently suggested that by merging this ex situ DNP approach with spatially-encoded "ultrafast" methods, a suitable starting point could arise for the acquisition of 2D spectra on hyperpolarized liquids. The present Article describes the experimental principles, potential features and current limitations of such integration between the two methodologies. It was found for a variety of small molecules that the new hyperpolarized ultrafast experiments could, for equivalent overall durations, provide heteronuclear correlation spectra at significantly lower concentrations than those currently achievable by conventional 2D NMR acquisitions. A variety of challenges still remain to be solved before bringing the full potential of this new integrated 2D NMR approach into fruition; these outstanding issues are also discussed.