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The Journal of Organic Chemistry|June 3, 2010
Profiling sulfonate ester stability: identification of complementary protecting groups for sulfonatesStephen C MillerJournal of Computational Chemistry|December 15, 2018
Computational investigation into the fluorescence of luciferin analoguesThom Vreven, Stephen C MillerChemical Communications (Cambridge, England)|January 7, 2011
Design and application of esterase-labile sulfonate protecting groupsLaert Rusha, Stephen C MillerOrganic Letters|July 18, 2018
Silicon Substitution in Oxazine Dyes Yields Near-Infrared Azasiline Fluorophores That Absorb and Emit beyond 700 nmAdam Choi, Stephen C MillerOrganic & Biomolecular Chemistry|January 25, 2017
Reductively-labile sulfonate ester protecting groups that are rapidly cleaved by physiological glutathioneAdam Choi, Stephen C MillerOrganic Letters|November 4, 2011
Synthesis of near-IR fluorescent oxazine dyes with esterase-labile sulfonate estersSteven M Pauff, Stephen C MillerThe FEBS Journal|December 13, 2019
Enzymatic promiscuity and the evolution of bioluminescenceSpencer T Adams, Stephen C MillerACS Chemical Neuroscience|July 31, 2015
Luciferins behave like drugsDavid M Mofford, Stephen C MillerThe Journal of Organic Chemistry|November 22, 2012
A trifluoroacetic acid-labile sulfonate protecting group and its use in the synthesis of a near-IR fluorophoreSteven M Pauff, Stephen C MillerCurrent Opinion in Chemical Biology|August 1, 2014
Beyond D-luciferin: expanding the scope of bioluminescence imaging in vivoSpencer T Adams, Stephen C MillerPageof 3