We spectroscopically investigate a pathway for the conversion of 23 Na 39 K Feshbach molecules into rovibronic ground state molecules via stimulated Raman adiabatic passage. Using photoassociation spectroscopy from the diatomic scattering threshold in the a 3 Σ + potential, we locate the resonantly mixed electronically excited intermediate stateswhich, due to their singlet-triplet admixture, serve as an ideal bridge between predominantly a 3 Σ + Feshbach molecules and pure X 1 Σ + ground state molecules. We investigate their hyperfine structure and present a simple model to determine the singlet-triplet coupling of these states. Using Autler-Townes spectroscopy, we locate the rovibronic ground state of the 23 Na 39 K molecule (| S = = ñ + X v N , 0, 0 1 ) and the second rotationally excited state N=2 to unambiguously identify the ground state. We also extract the effective transition dipole moment from the excited to the ground state. Our investigations result in a fully characterized scheme for the creation of ultracold bosonic 23 Na 39 K ground state molecules. 23 Na 40 K have been created using excited states in energetically higher D 1 Π and d 3 Π potentials [13]; not shown in figure 1(a).