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2. Formation of Organic Acids and Carbonyl Compounds in n‐Butane Oxidation via γ‐Ketohydroperoxide Decomposition

4. Direct kinetic measurements and theoretical predictions of an isoprene-derived Criegee intermediate.

5. The reaction of hydroxyl and methylperoxy radicals is not a major source of atmospheric methanol.

13. New Instrument for Time-Resolved OH and HO2Quantification in High-Pressure Laboratory Kinetics Studies

23. Bimolecular Reaction of Methyl-Ethyl-Substituted Criegee Intermediate with SO2

31. Chemical Kinetics at SNL.

42. Correction to "OH Roaming and Beyond in the Unimolecular Decay of the Methyl-Ethyl-Substituted Criegee Intermediate: Observations and Predictions".

43. Insertion products in the reaction of carbonyl oxide Criegee intermediates with acids: Chloro(hydroperoxy)methane formation from reaction of CH2OO with HCl and DCl

47. The impact of the third O2 addition reaction network on ignition delay times of neo-pentane.

50. Reaction mechanisms of a cyclic ether intermediate: Ethyloxirane

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