Volume 12 Issue 1 (2006) Table of Contents

*Indicates author to whom correspondence should be addressed

Pages 1–14

Derivatization in mass spectrometry – 7. On-line derivatisation/degradation

John M. Halket
Drug Control Centre, King’s College London, Franklin-Wilkins Building, Stamford Street, London SE1 9NH, UK. E-mail: john.halket@kcl.ac.uk
Vladimir G. Zaikin
Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky prospect 29, 119991 Moscow, Russia. E-mail: zaikin@ips.ac.ru

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DOI: 10.1255/ejms.785

Pages 15–18

Cationization versus surface activity—the effect on electrospray ionization

Magdalena Frańska,a,* Ilona Przybysz,a Magdalena Borkowskaa and Tomasz Kozikb
aPoznań University of Technology, Institute of Chemistry, Piotrowo 3, 60-965 Poznań, Poland. E-mail: Magdalena.Franska@fct.put.poznan.pl
bAdam Mickiewicz University, Faculty of Chemistry, Grunwaldzka 6, 60-780 Poznań, Poland

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DOI: 10.1255/ejms.788

Pages 19–24

Generation of alkoxide anions from a series of aliphatic diols and alcohols and their ion-molecule reactions with carbon dioxide in the gas phase

M. Ravi Kumar, S. Prabhakar, T. Jagadeshwar Reddy and M. Vairamani*
National Center for Mass Spectrometry, Indian Institute of Chemical Technology, Hyderabad, India-500 007

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DOI: 10.1255/ejms.791

Pages 25–30

Electron ionization mass spectra and tautomerism of 2-phenacylpyridines

Olli Martiskainen,a Ryszard Gawinecki,b Borys Ošmiałowskib and Kalevi Pihlajaa,*
aStructural Chemistry Group, Department of Chemistry, University of Turku, FI-20014 Turku Finland. E-mail: kpihlaja@utu.fi
bDepartment of Chemistry, Technical and Agricultural University, Seminaryjna 3, PL-85-326 Bydgoszcz, Poland

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DOI: 10.1255/ejms.786

Pages 31–36

Efficient clustering of cyclic sulfonium salts applying liquid secondary ion mass spectrometry

Rosaria Cozzolino, Richard T. Gallagher and Thomas Drewello*
Department of Chemistry, University of Warwick, Coventry CV4 7AL, UK

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DOI: 10.1255/ejms.789

Pages 37–42

Electrospray ionization tandem mass spectrometry determined regioisomeric structures of disubstituted β-cyclodextrin derivatives

Hatsuo Yamamura,a,* Toshifumi Iwata,a Masao Kawaia and Akihiro Satob
aGraduate School of Engineering, Gokiso-cho, Showa-ku, Nagoya, Aichi 466-8555, Japan
bJasco International Co., Ltd, 11-10 Myojin-cho 1-chome Hachioji, Tokyo 192-0046, Japan

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DOI: 10.1255/ejms.793

Pages 43–50

Negative electrospray, ion trap multistage mass spectrometry of synthetic fragments of the O-PS of Vibrio cholerae O:1

Slávka Bekešová,a,* Vladimír Kováčik,a Josef Chmelíkb and Pavol Kováčc
aInstitute of Chemistry, Slovak Academy of Sciences, Dúbravská cesta 9, 845 38 Bratislava, Slovakia. E- mail: chembeke@savba.sk
bInstitute of Analytical Chemistry, Czech Academy of Sciences, Veveří 97, 811 42 Brno, Czech Republic
cNIDDK, National Institute of Health, Bethesda, Maryland 20892-0815, USA

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DOI: 10.1255/ejms.790

Pages 51–62

Mass spectrometric sequencing and acylation character analysis of C-terminal anchoring segment from Influenza A hemagglutinin

Marina V. Serebryakova
Orekhovich Institute of Biomedical Chemistry, Russian Academy of Medical Sciences, Moscow 119992, Russia
Larisa V. Kordyukova* and Ludmila A. Baratova
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119992, Russia. E-mail: kord@belozersky.msu.ru
Stanislav G. Markushin
Andjaparidze Institute for Viral Preparations, Moscow 115088, Russia

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DOI: 10.1255/ejms.792

Pages 63–70

Letter: Some more aspects of formation and stability of the protonated serine octamer cluster

Ulf Mazurek
Department of Physical Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel. E-mail: ykv@chem.ch.huji.ac.il

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DOI: 10.1255/ejms.783

Pages 71–74

Letter: Radical ion and protonated molecule formation with retinal in electrospray and nanospray

Thais Guaratinia,b,c, Paul J. Gatesb, Karina H. M. Cardozob,c,, Patrícia M. B. G. M.Camposa, Pio Colepicoloc, and Norberto P. Lopesa,b,*
a Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Via do Café S/N, CEP 14040-903, Ribeirão Preto-SP, Brazil. E-mail: npelopes@fcfrp.usp.br
bSchool of Chemistry, University of Bristol, Cantock’s Close, Bristol, BS8 1TS, UK
cDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, Av Professor Lineu Prestes, 748 CP 20780, CEP 05508900, São Paulo-SP, Brazil

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DOI: 10.1255/ejms.784

Pages 75–78

Letter: Steric effects in electrospray-tandem mass spectrometry of 11βnitrates of estrane series.

V.I. Kadentsev,* A.O. Chizhov, O.S. Chizhov, and O.N. Krupinova
N.D. Zelinsky Institute of Organic Chemistry, RAS 119991, 47 Leninsky Prosp., Moscow, Russian Federation. Email: vkadents@ioc.ac.ru
V.M. Rzheznikov and L.E. Golubovskaya
Endocrinological Research Centre, RAMS 117036, 11 Dmitriya Ul’yanova Str., Moscow, Russian Federation

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DOI: 10.1255/ejms.787


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