Renewable phenols derived from biomass sources often contain methoxy groups that alter the properties of derivative polymers. To evaluate the impact of o-methoxy groups on the performance characteristics of cyanate ester resins, three bisphenols derived from the renewable phenol creosol were deoxygenated by conversion to ditriflates followed by palladium-catalyzed elimination and hydrolysis of the methoxy groups. The deoxygenated bisphenols were then converted to the following cyanate ester resins: bis(4-cyanato-2-methylphenyl)methane (16), 4,4'-(ethane-1,1'-diy1)bis-(1-cyanato-3-methylbenzene) (17), and 4,4'-(propane-1,1'-diy1)bis(1-cyanato-3-methylbenzene) (18). The physical properties, cure chemistry, and thermal stability of these resins were evaluated and compared to those of cyanate esters derived from the oxygenated bisphenols. 16 and 18 had melting points 37 and >95 degrees C lower, respectively, than the oxygenated versions, while 17 had a melting point 14 degrees C higher. The T-g's of thermosets generated from the deoxygenated resins ranged from 267 to 283 degrees C, up to 30 degrees C higher than the oxygenated resins, while the onset of thermal degradation was 50-80 degrees C higher. The deoxygenated resins also exhibited water uptakes up to 43% lower and wet T(g)s up to 37 degrees C higher than the oxygenated resins. TGA-FTIR of thermoset networks derived from 16-18 revealed a different decomposition mechanism compared to the oxygenated resins. Instead of a low-temperature pathway that resulted in the evolution of phenolic compounds, 16-18 had significantly higher char yields and decomposed via evolution of small molecules including isocyanic acid, CH4, CO2, and NH3.