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

✍ Scribed by S. Pounds; M. J. Hickey; L. P. Kingston; A. N. Mather; D. J. Wilkinson; G. V. Sidorov; Yu. B. Zverkov; N. F. Myasoedov; I. L. Karpenko; E. A. Shirokova; D. M. Yanvarev; M. V. Yasko; Yu. S. Skoblov; A. B. Susan; N. F. Myasoedov; I. Y. Nagaev; V. P. Shevchenko; A. B. Susan; G. Rotert; Jens Krüger; Gregor Fels; F. Wuest; P. Mäding; J. Zessin; U. Pleiß; F. Wüst; A. J. Bloom; V. Derdau; R. Oekonomopulos; G. Schubert; H. Andres; P. Burtscher; Y. Metz; Th. Moenius; F. Kaegi; Y. Metz; I. Rodriguez; R. Ruetsch; C. G. M. Janssen; B. Verreet; H. A. C. Lenoir; J. B. A. Thijssen; Rolf P. Stuerm; Andreas Krins; E. Rausch; M. Breyer; K. Hucke; D. Gaefke; K. Schmeer


Publisher
John Wiley and Sons
Year
2004
Tongue
French
Weight
479 KB
Volume
47
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

S Pounds [PerkinElmer Life and Analytical Sciences, Inc., USA]—Preparation of carrierfree [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 ‘‐Azido3’‐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 βAmino 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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