18F-FDG Radiosynthesis: A Landmark in the History of PET (perspective on “Efficient Stereospecific Synthesis of No-Carrier-Added 2-[18F]fluoro-2-Deoxy-D-Glucose Using Aminopolyether Supported Nucleophilic Substitution” J Nucl Med. 1986;27:235

18F-FDG Radiosynthesis: A Landmark in the History of PET (perspective on “Efficient Stereospecific Synthesis of No-Carrier-Added 2-[18F]fluoro-2-Deoxy-D-Glucose Using Aminopolyether Supported Nucleophilic Substitution” J Nucl Med. 1986;27:235–238)

Published:2020-12 Issue:Supplement 2 Volume:61 Page:105S-109S
ISSN:0161-5505
Container-title:Journal of Nuclear Medicine
language:en
Short-container-title:J Nucl Med

Author:

Fowler Joanna S.

Publisher

Society of Nuclear Medicine

Subject

Radiology Nuclear Medicine and imaging

Reference5 articles.

1. The [18F]fluorodeoxyglucose method for the measurement of local cerebral glucose utilization in man.

2. Efficient stereospecific synthesis of NCA 2-[18F]fluoro-2-deoxy-D-glucose using aminopolyether supported nucleophilic substitution;Hamacher;J Nucl Med.,1986

3. Mapping of Functional Neural Pathways by Autoradiographic Survey of Local Metabolic Rate with [ 14 C]Deoxyglucose

4. Initial and subsequent approach for the synthesis of 18FDG

5. Labeled 2-deoxy-D-glucose analogs: 18F-labeled 2-deoxy-2-fluoro-D-glucose, 2-deoxy-2-fluoro-D-mannose and 14C-2-deoxy-2-fluoro-S-glucose;Ido;J Labelled Comp Radiopharm.,1978

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