^*Indicates author to whom correspondence should be addressed

A simple algorithm for the calculation of kinetic energy release distributions

Zoltán Szilágyi and Károly Vékey
Central Research Institute for Chemistry, Hungarian Academy of Sciences, H-1025 Budapest, Pusztaszeri út 59–67, Hungary.

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DOI: 10.1255/ejms.86

Ion–molecule reactions of charged thiols with neutral epoxides in the collision cell of a tandem quadrupole mass spectrometer. A model for invivo biomolecule reactions

Boris V. Rozynov
Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Science, 117871 Moscow V-437, Russia.
Douglas W. Kuehl
US Environmental Protection Agency, Environmental Research Laboratory–Duluth, Duluth, MN 55804, USA.
Robert M. Carlson^*
Department of Chemistry, University of Minnesota–Duluth, Duluth, MN 55812, USA.

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DOI: 10.1255/ejms.87

Ortho effects: a mechanistic study

Anja Barkow, Steffen Pilotek and Hans-Friedrich Grützmacher^*
Lehrstuhl I für Organische Chemie, Fakultät für Chemie,Universität Bielefeld, Universitätsstr. 25, D-33615 Bielefeld, Germany.

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DOI: 10.1255/ejms.88

Acetone chemical ionization studies. VIII: pyridine derivatives

M. Vairamani,^* S. Prabhakar, N. Prasada Raju and G.K. Viswanadha Rao
Indian Institute of Chemical Technology, Hyderabad 500 007, India.

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DOI: 10.1255/ejms.89

The chemistry of ionized ethyl glycolate, HOCH₂CO₂C₂H₅^·+, and its enol isomer, HOCH=C(OH)OC₂H₅^·+. Formation of ionized and neutral trihydroxyethylene

Dennis Suh, James T. Francis and Johan K. Terlouw^*
Department of Chemistry, McMaster University, Hamilton, Ontario L8S 4M1, Canada.
Peter C. Burgers
Hercules European Research Center BV, Nijverheidsweg 60, 3771 ME Barneveld, The Netherlands.
Richard D. Bowen
Chemistry and Chemical Technology, University of Bradford, Bradford, West Yorkshire, BD7 1DP, UK.

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DOI: 10.1255/ejms.90

Electron impact mass spectrometry of aromatic azoethers

Stelian Radu
Department of Chemistry, Faculty of Sciences, University of Craiova, A.I. Cuza 13, 1100 Craiova, Romania.

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DOI: 10.1255/ejms.91

Liquid chromatography/electrospray tandem mass spectrometry of amino acid conjugates of jasmonic acid under positive and negative ionisation

Jürgen Schmidt,^* Robert Kramell and Gernot Schneider
Institut für Pflanzenbiochemie, Weinberg 3, D-06120 Halle/S., Germany.

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DOI: 10.1255/ejms.92

Nanoelectrospray mass spectrometry/mass spectrometry for the analysis of modified oligoribonucleotides

M.A. Wolter^* and J.W. Engels
Institute for Organic Chemistry, Johann Wolfgang Goethe-University, Marie-Curie-Strasse 11, 60054 Frankfurt, Germany.

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DOI: 10.1255/ejms.93

Letter: Differentiation of S-cis and S-trans conformations of acyclic dienes by electron impact mass spectrometry

J-F. Rontani^* and V. Grossi
Centre d’Océanologie de Marseille—URA 41, Faculté des Sciences de Luminy—case 901, 13288 Marseille, France.

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DOI: 10.1255/ejms.94

Letter: Reactions in molecular clusters: proton transfer to small amino acids

Anja Meffert and Jürgen Grotemeyer
Institut für Physikalische Chemie der Universität Würzburg, Marcusstrasse 9–11, 97070 Würzburg, Germany.

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DOI: 10.1255/ejms.95