Publications by authors named "Olle Matsson"

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Mechanistic insights into the Pd-catalyzed direct amination of allyl alcohols: evidence for an outer-sphere mechanism involving a palladium hydride intermediate.
Supaporn Sawadjoon, Per J R Sjöberg, Andreas Orthaber, Olle Matsson, Joseph S M Samec

Chemistry· February 2014

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[Poisonous reading].
Olle Matsson

Lakartidningen· November 2013

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Nitrogen kinetic isotope effects for the monoamine oxidase B-catalyzed oxidation of benzylamine and (1,1-(2)H2)benzylamine: nitrogen rehybridization and CH bond cleavage are not concerted.
Susanna MacMillar, Dale E Edmondson, Olle Matsson

J Am Chem Soc· August 2011

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Determining the transition-state structure for different SN2 reactions using experimental nucleophile carbon and secondary alpha-deuterium kinetic isotope effects and theory.
Kenneth C Westaway, Yao-ren Fang, Susanna MacMillar, Olle Matsson, Raymond A Poirier

J Phys Chem A· October 2008

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A new insight into using chlorine leaving group and nucleophile carbon kinetic isotope effects to determine substituent effects on the structure of SN2 transition states.
Kenneth C Westaway, Yao-ren Fang, Susanna MacMillar, Olle Matsson, Raymond A Poirier

J Phys Chem A· August 2007

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The effect of solvent on the structure of the transition state for the S(N)2 reaction between cyanide ion and ethyl chloride in DMSO and THF probed with six different kinetic isotope effects.
Yao-ren Fang, Susanna MacMillar, Jonas Eriksson, Magdalena Kołodziejska-Huben, Agnieszka Dybała-Defratyka, Olle Matsson

J Org Chem· June 2006

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A new interpretation of chlorine leaving group kinetic isotope effects; a theoretical approach.
Agnieszka Dybała-Defratyka, Michał Rostkowski, Olle Matsson, Kenneth C Westaway, Piotr Paneth

J Org Chem· July 2004

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Experimental and theoretical multiple kinetic isotope effects for an SN2 reaction. An attempt to determine transition-state structure and the ability of theoretical methods to predict experimental kinetic isotope effects.
Yao-Ren Fang, Ying Gao, Per Ryberg, Jonas Eriksson, Magdalena Kołodziejska-Huben, Olle Matsson

Chemistry· June 2003

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The mechanism of base-promoted HF elimination from 4-fluoro-4-(4-nitrophenyl)butan-2-one is E1cB. evidence from double isotopic fractionation experiments.
Per Ryberg, Olle Matsson

J Org Chem· February 2002

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