EJMS Table of Contents

European Journal of Mass Spectrometry (EJMS)

Eur. J. Mass Spectrom. Volume 10 Issue 1 (2004)


Pages 1–19
doi: 10.1255/ejms.619
Derivatization in mass spectrometry. 3. Alkylation(arylation)
John M. Halket
Drug Control Centre, King's College London, Franklin-Wilkins Building, Stamford Street, London SE1 9NN, UK. E-mail: john.halket@kcl.ac.ukVladimir G. Zaikin
Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow, Russia. E-mail: zaikin@ips.ac.ru

Pages 21–26
doi: 10.1255/ejms.622
Ion/molecule reactions of isomeric bromobutene radical cations with ammonia
Hans-Friedrich Grützmacher* and Michael Büchner
Fakultät für Chemie der Universität Bielefeld, Universität Bielefeld, Postfach 10 01 31, D-33501 Bielefeld, Germany. E-mail: hans-friedrich.gruetzmacher@uni-bielefeld.de

Pages 27–37
doi: 10.1255/ejms.624
Depression of the apparent chiral recognition ability obtained in the host–guest complexation systems by electrospray and nano-electrospray ionization mass spectrometry
Masami Sawada,* Yoshio Takai and Hitoshi Yamada
Materials Analysis Center, The Institute of Scientific and Industrial Research, Osaka University, Ibaraki, Osaka 567-0047, Japan
Muneyoshi Yoshikawa and Ryuichi Arakawa
Department of Applied Chemistry, Kansai University, Suita, Osaka 564-0073, Japan
Hiroyuki Tabuchi, Mikio Takada and Jyuichi Tanaka
Faculty of Engineering, Osaka Institute of Technology, Asahi-ku, Osaka 535-0002, Japan
Motohiro Shizuma*
Technochemistry Department, Osaka Municipal Technical Research Institute, Joto-ku, Osaka 536-8553, Japan
Hiroshi Yamaoka
Faculty of Science, Osaka Women’s University, Sakai, Osaka 567-0035, Japan
Keiji Hirose, Kazuo Fukuda and Yoshito Tobe
Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka 560-8531, Japan

Pages 39–46
doi: 10.1255/ejms.582
Methylating peptides to prevent adduct ion formation also directs cleavage in collision-induced dissociation mass spectrometry
Clement Poon, Harvey Kaplan and Paul M. Mayer*
Chemistry Department, University of Ottawa, 10 Marie Curie, Ottawa, Canada K1N 6N5

Pages 47–55
doi: 10.1255/ejms.587
Structure elucidation of unsaturated fatty acids after vicinal hydroxylation of the double bonds by negative electrospray ionisation low-energy tandem mass spectrometry
Morten K. Moe* and Einar Jensen
Institute of Pharmacy, Faculty of Medicine, University of Tromsø, N-9037 Tromsø, Norway

Pages 57–62
doi: 10.1255/ejms.595
Cyclization of N,N-dialkylditiocarbamate and alkylxanthate derivatives of polyhalogenated pyridines in gas and liquid phases
Tatiana Yu. Samguina, Vladislav V. Lobodin, Nadezhda K. Karakhanova and Albert T. Lebedev*
Organic Chemistry Department, Moscow State University, Leninskie gori 1/3, Moscow 119899, Russia. E-mail: lebedev@org.chem.msu.ru
Aleksey M. Sipyagin
Institute of Problems of Chemical Physics, RAS, Chernogolovka 142432, Russia

Pages 63–88
doi: 10.1255/ejms.625
High-energy collision-induced dissociation of oxosteroids derivatised to Girard hydrazones
William J. Griffiths*
Department of Pharmaceutical & Biological Chemistry, The School of Pharmacy, University of London, 29-39 Brunswick Square, London WC1N 1AX, UK and Department of Medical Biochemistry & Biophysics, Karolinska Institutet, SE-17177 Stockholm, Sweden. E-mail: william.griffiths@ulsop.ac.uk
Gunvor Alvelius, Suya Liu and Jan Sjövall
Department of Medical Biochemistry & Biophysics, Karolinska Institutet, SE-17177 Stockholm, Sweden

Pages 89–99
doi: 10.1255/ejms.626
Investigation of methods suitable for the matrix-assisted laser desorption/ionization mass spectrometric analysis of proteins from ribonucleoprotein complexes
Moo-Jin Suh and Patrick A. Limbach*
Rieveschl Laboratories for Mass Spectrometry, Department of Chemistry, PO Box 210172, University of Cincinnati, Cincinnati, OH 45221, USA. E-mail: Pat.Limbach@uc.edu

Pages 101–108
doi: 10.1255/ejms.592
Estimation of the molecular mass range of the tar from pyrolysis of casein by gas chromatography-mass spectrometry, probe mass spectrometry and size exclusion chromatography with 1-methyl-2-pyrrolidinone as eluent
B. Purevsuren, B. Avid and Ya. Davaajav
Institute of Chemistry and Chemical Technology, Mongolian Academy of Sciences, Ulaanbaatar,51, Mongolia
A.A. Herod,* R. Kandiyoti and T.J. Morgan
Department of Chemical Engineering and Chemical Technology, South Kensington Campus, Imperial College London, London SW7 2AZ, UK

Pages 109–120
doi: 10.1255/ejms.544
Matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry. A comparison of fragmentation patterns of linear dextran obtained by in-source decay, post-source decay and collision-induced dissociation and the stability of linear and cyclic glucans studied by in-source decay
Sajid Bashir,*,a,b Anastassios E. Giannakopulos and Peter J. Derrick
Institute of Mass Spectrometry, University of Warwick, Coventry CV4 7AL, UK
Peter Critchley
Department of Chemistry, University of Warwick, Coventry CV4 7AL, UK
Andrew Bottrillc
Institute of Mass Spectrometry, University of Warwick, Coventry, CV4 7AL, UK
Henry D. Padley
United States Army, Chemical Corp, Fort Bragg, North Carolina 28314, USA

Pages 121–134
doi: 10.1255/ejms.588
Characterization and de novo sequencing of Atlantic salmon vitellogenin protein by electrospray tandem and matrix-assisted laser desorption/ionization mass spectrometry
Joseph Banoub*
Special Projects, Oceans Division, Northwest Atlantic Fisheries Center, St John’s, Newfoundland A1C 5X1, Canada and Department of Biochemistry, Memorial University of Newfoundland, St. John’s, Newfoundland A1C 5S7, Canada. E-mail: banoubjo@dfo-mpo.gc.ca or joebanoub@attglobal.net
Alejandro Cohen
Department of Biochemistry, Memorial University of Newfoundland, St. John’s, Newfoundland A1C 5S7, Canada
Atef Mansour
Aquaculture Research Section, Science, Oceans and Environment Branch, Oceans Programs Division, Northwest Atlantic Fisheries Center, St John’s, Newfoundland A1C 5X1, Canada
Pierre Thibault
Protein Analysis, Caprion Pharmaceuticals, 7150 Alexander Fleming, Montreal, Quebec H4S 2C8, Canada
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