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Journal of the American Chemical Society|June 1, 2016
How Acid-Catalyzed Decarboxylation of 2,4-Dimethoxybenzoic Acid Avoids Formation of Protonated CO2Graeme W Howe, Adelle A Vandersteen, Ronald KlugerChemical Communications (Cambridge, England)|May 8, 2010
Protein-protein coupling and its application to functional red cell substitutesRonald Kluger, Jonathan S Foot, Adelle A VandersteenThe Journal of Organic Chemistry|July 19, 2012
Protonated carbonic acid and reactive intermediates in the acidic decarboxylation of indolecarboxylic acidsAdelle A Vandersteen, Scott O C Mundle, Ronald KlugerJournal of the American Chemical Society|October 7, 2017
Carbon Kinetic Isotope Effects and the Mechanisms of Acid-Catalyzed Decarboxylation of 2,4-Dimethoxybenzoic Acid and CO<sub>2</sub> Incorporation into 1,3-DimethoxybenzeneAdelle A Vandersteen, Graeme W Howe, Barbara Sherwood Lollar, et al.Rapid Communications in Mass Spectrometry : RCM|July 4, 2013
Pressure-monitored headspace analysis combined with compound-specific isotope analysis to measure isotope fractionation in gas-producing reactionsScott O C Mundle, Adelle A Vandersteen, Georges Lacrampe-Couloume, et al.The Journal of Organic Chemistry|November 22, 2013
Carbon kinetic isotope effects reveal variations in reactivity of intermediates in the formation of protonated carbonic acidAdelle A Vandersteen, Scott O C Mundle, Georges Lacrampe-Couloume, et al.Pageof 1