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11th conference of the central european division e.V. of the international isotope society
Author(s) -
Pounds S.,
Hickey M. J.,
Kingston L. P.,
Mather A. N.,
Wilkinson D. J.,
Sidorov G. V.,
Zverkov Yu. B.,
Myasoedov N. F.,
Karpenko I. L.,
Shirokova E. A.,
Yanvarev D. M.,
Yasko M. V.,
Skoblov Yu. S.,
Susan A. B.,
Myasoedov N. F.,
Nagaev I. Y.,
Shevchenko V. P.,
Susan A. B.,
Rotert G.,
Krüger Jens,
Fels Gregor,
Wuest F.,
Mäding P.,
Zessin J.,
Pleiß U.,
Wüst F.,
Bloom A. J.,
Derdau V.,
Oekonomopulos R.,
Schubert G.,
Andres H.,
Burtscher P.,
Metz Y.,
Moenius Th.,
Kaegi F.,
Metz Y.,
Rodriguez I.,
Ruetsch R.,
Janssen C. G. M.,
Verreet B.,
Lenoir H. A. C.,
Thijssen J. B. A.,
Stuerm Rolf P.,
Krins Andreas,
Rausch E.,
Breyer M.,
Hucke K.,
Gaefke D.,
Schmeer K.
Publication year - 2004
Publication title -
journal of labelled compounds and radiopharmaceuticals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.432
H-Index - 47
eISSN - 1099-1344
pISSN - 0362-4803
DOI - 10.1002/jlcr.814
Subject(s) - chemistry , stereochemistry , moiety
S Pounds [PerkinElmer Life and Analytical Sciences, Inc., USA]— Preparation of carrier – free [ Methyl ‐ 3 H ] Methyl Nosylate and its Use as a Radiochemically Stable Methylating reagent . DJ Wilkinson , AN Mather , MJ Hickey , LP Kingston [Astra Zeneca, UK]— Tritio‐Dehalogenation: New Variants on an Old Theme . VG Sidorov , YB Zverkov , NF Myasoedov , IMG , Russia ; IL Karpenko , EA Shirokova , DM Yanvarev , MV Yasko , YS Skoblov [EIMB, Russia], AB Susan , [IICH, USA]— The Syntheses of Labeled 3 ‘‐ Azido ‐ 3 ’‐ Deoxythymidine Derivatives Displaying Anti‐HIV Activity . NF Myasoedov , IY Nagaev , VP Shevchenko [IMG, Russia], AB Susan [IICH, USA], G Rotert [Abbott, USA]— Synthesis of Radiolabeled [ 3 H ] ABT‐578 for ADME Studies . J Krueger , E Linnemann , G Fels [University of Paderborn, Germany]—(‐)‐[ 3 H ] Galanthamine – Labelling , Derivatization , and Application as Photoaffinity Probe . F Wuest [Research Centre Rossendorf, Germany]— Carbon ‐11 Labeled Compounds in the Development of Pharmaceuticals . P Maeding , J Zessin , F Wüst [Research Centre Rossendorf, Germany], U Pleiss [Bayer HealthCare AG, Germany]— 11 C‐ Labeling of a Taxane Derivative by [1‐ 11 C] Acetylation . J Bloom [Amersham Biosciences, UK]— The Preparation of 2‐ Methyl [ ring ‐2‐ 14 C] benzyl chloride . V Derdau , R Oekonomopulos , G Schubert , H Heitsch [Aventis Pharma Deuschland GmbH, Germany]— Synthesis of 14 C Labeled Angiotensin ‐(1‐7)‐ Receptor Agonist AVE 0991. H Andres , P Burtscher , Y Metz , T Moenius [Novartis Pharma AG, Switzerland]— C ‐14 Labeling of the β ‐ Amino Carboxyl Moiety–Alternatives to the Acrylate Approach . F Kaegi , Y Metz , I Rodriguez , R Ruetsch [Novartis Pharma AG, Switzerland]— Effective Carbon ‐14 Labelling under Microwave Irradiation . CGM Janssen , B Verreet , HAC Lenoir , JBA Thijssen [Johnson & Johnson, Belgium]— Stable Isotope Labeled Compounds as Internal Standards for LC‐MS/MS , Requirements and Some Synthetic Approaches . RP Stuerm [SafPro AG, Switzerland]— Models for Calculating the Radiation Dose after Incorporation of 3 H and 14 C . A. Krins [VKTA Nuclear Engineering and Analytics e.V., Germany]— Dosimetry of C ‐14 Labeled Organic Compounds . E Rausch [Raytest GmbH, Germany], M Breyer , K Hucke , D Gaefke , K Schmeer [Bayer HealthCare AG, Germany]— A New Option of 14 C‐ Detection in Combination with Micro HPLC .

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