Further Radiopharmaceuticals for Positron Emission Tomography and New Strategies for Their Production, Volume 2

Zusatztext

This book describes methods and procedures for preparing PET radiopharmaceuticals, and highlights new methods for conducting radiochemical reactions with carbon-11 (C11) and fluorine-18 (F18), which are two of the most commonly used radionuclides in positron emission tomography (PET) imaging.<br /><br />     Provides reliable methods for radiochemical syntheses and reactions, including all essential information to duplicate the procedure<br />     Eliminates the time-consuming process of searching journal articles and extracting pertinent details from lengthy experimental sections or supporting information<br />     Focuses on an emerging and important area for pharmaceutical and medical applications<br />     Encompasses technical, regulatory, and application aspects<br />     Includes solid-phase radiochemistry, transition-metal catalyzed radiochemistry, microfluidics, click chemistry, green radiochemistry and new strategies for radiopharmaceutical quality control

Autorenportrait

<b>Peter J. H. Scott</b>is an Assistant Professor in the Department of Radiology at the University of Michigan Medical School (USA), Director of the University of Michigan PET Center (USA) and a member of the Interdepartmental Program in Medicinal Chemistry. Professor Scott edited<i>Linker Strategies in Solid-Phase Organic Synthesis</i> (also from Wiley) and is the series editor for both the Wiley Series on Radiochemical Syntheses and the Wiley Series on Solid Phase Organic Syntheses.

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