Details

Autor(en) / Beteiligte

• 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.
• Nagaev, I. Y.
• Shevchenko, V. P.
• 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.
• 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.

Titel

11th conference of the central european division e.V. of the international isotope society

Ist Teil von

• Journal of labelled compounds & radiopharmaceuticals, 2004-03, Vol.47 (4), p.243-288

Ort / Verlag

Chichester, UK: John Wiley & Sons, Ltd

Erscheinungsjahr

2004

Quelle

Wiley Online Journals

Beschreibungen/Notizen

• S Pounds [PerkinElmer Life and Analytical Sciences, Inc., USA]—Preparation of carrier – free [Methyl‐3H] 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 [3H]ABT‐578 for ADME Studies. J Krueger, E Linnemann, G Fels [University of Paderborn, Germany]—(‐)‐[3H]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]—11C‐Labeling of a Taxane Derivative by [1‐11C] Acetylation. J Bloom [Amersham Biosciences, UK]—The Preparation of 2‐Methyl [ring‐2‐14C] benzyl chloride. V Derdau, R Oekonomopulos, G Schubert, H Heitsch [Aventis Pharma Deuschland GmbH, Germany]—Synthesis of 14C 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 3H and 14C. 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 14C‐Detection in Combination with Micro HPLC.