^*Indicates author to whom correspondence should be addressed

The C₃H₆O^+• fragment from 1,4-dioxane^+• revisited

R. Thissen
LPCR, Université Paris Sud, 91405 Orsay, France.
H.E. Audier, J. Chamot-Rooke and P. Mourgues
DCMR, UMR CNRS 7651, Ecole Polytechnique, 91128 Palaiseau, France.

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DOI: 10.1255/ejms.260

High-performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry of phospholipids in Natronobacterium magadii

Di-Fei Qiu^* and Xiao-Yao Xiao
Department of Chemistry, Hunan University, Hunan Changsha 410082, People’s Republic of China.
Terence J. Walton
Biochemistry Research Group, School of Biological Sciences, University of Wales Swansea, Swansea SA2 8PP, UK.
Marguerite P.L. Games and David E. Games
Mass Spectrometry Research Unit, University of Wales Swansea, Swansea SA2 8PP, UK..

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DOI: 10.1255/ejms.262

Electrospray ionization and atmospheric pressure ionization mass spectrometry of stable organic radicals

Jürgen O. Metzger and Jens Griep-Raming
Department of Chemistry, Carl von Ossietzky University Oldenburg, Carl-von-Ossietzky-Straée 9-11, D-26129 Oldenburg, Germany.

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DOI: 10.1255/ejms.263

Letter: The use of electrospray ionization mass spectrometry to distinguish the lot-to-lot heterogeneity of an antigen specific monoclonal antibody from a specific cellular clone

Maciej Adamczyk^*, John C. Gebler, Charles A. Harrington and Austin F. Sequeira
Abbott Laboratories, Diagnostics Division, Department of Chemistry (9-NM), Building AP-20, 100 Abbott Park Road, IL 60064-6016, USA. E-mail: maciej.adamczyk@abbott.com

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DOI: 10.1255/ejms.264

Thermochemistry of organic and heteroorganic species. Part V. Photoionization studies of isomerization and fragmentation of polysubstituted cyclopropenes: 3-methyl-3-acetyl- and related compounds

I.N. Domnin
Department of Chemistry, St Petersburg University,198904 St Petersburg, Peterhof, University pr. 2, Russia.
V.V. Takhistov
Centre of Ecological Safety of Russian Academy of Sciences, 197042 St Petersburg, Russia.
D.A. Ponomarev^*
Department of Chemical Engineering, St Petersburg Forest Technical Academy, 194021 St Petersburg, Russia.

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DOI: 10.1255/ejms.265

Electron impact-induced mass spectral study of new isomeric N-substituted hydrazones of ortho-, meta– and para– hydroxybenzaldehydes

E. Wyrzykiewicz and D. Prukala
Department of Mass Spectrometry of Organic Coumpounds, Faculty of Chemistry, Adam Mickiewicz University, Grunwaldzka 6, 60 -780 Poznan, Poland

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DOI: 10.1255/ejms.274

The C₃H₆O^+· fragment from 1,4-dioxane^+· revisited

José M. Vega-Pérez^*, José I. Candela, Felipe Alcudia and Fernando Iglesias-Guerra^*
Departamento de Química Orgánica y Farmacéutica, Facultad de Farmacia, Universidad de Sevilla, E-41071 Sevilla, Spain.

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DOI: 10.1255/ejms.275

Reductive degradation of O-acyl oximes under fast-atom bombardment conditions

Shizuyo Horiyama,^* Kiyoko Suwa, Masae Yamaki, Hiromi Kataoka and Toyoshi Katagi
Faculty of Pharmaceutical Sciences, Mukogawa Women’s University, 11–68 Koshien Kyuban-cho, Nishinomiya 663-8179, Japan.
Mitsuo Takayama
Faculty of Pharmaceutical Sciences, Toho University, 2-2-1 Miyama, Funabashi, Chiba 274-8510, Japan.

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DOI: 10.1255/ejms.276

Gas chromatography/mass spectrometry analysis of alkaloids in betel nut (Areca catechu)

Ron Self, R. Alan Jones and David K. Holdsworth
School of Chemical Sciences, University of East Anglia, Norwich, NR4 7TJ, UK.

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DOI: 10.1255/ejms.277

Mass spectral characteristics of C₁₉ and C₂₀ tricyclic terpanes detected in Latrobe Tasmanite oil shale

Paul F. Greenwood^* and Simon C. George
CSIRO Division of Petroleum Resources, PO Box 136, North Ryde, NSW 1670, Australia. E-mail: Paul.Greenwood@syd.dpr.csiro.au.

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DOI: 10.1255/ejms.278

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