Synthesis of p-(Di-tert-butyl[18F]fluorosilyl)benzaldehyde ([18F]SiFA-A) with High Specific Activity by Isotopic Exchange: A Convenient Labeling Synthon for the 18F-Labeling of N-amino-oxy Derivatized Peptides-Reference-Cited by-同舟云学术

Synthesis of p-(Di-tert-butyl[18F]fluorosilyl)benzaldehyde ([18F]SiFA-A) with High Specific Activity by Isotopic Exchange: A Convenient Labeling Synthon for the 18F-Labeling of N-amino-oxy Derivatized Peptides

Published:2007-11-01 Issue:6 Volume:18 Page:2085-2089
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Schirrmacher Esther¹,Wängler Björn¹,Cypryk Marek¹,Bradtmöller Gerrit¹,Schäfer Martin¹,Eisenhut Michael¹,Jurkschat Klaus¹,Schirrmacher Ralf¹

Affiliation:

1. Lady Davis Institute, Jewish General Hospital, and Montreal Neurological Institute, McGill University, Montreal, Canada, Department of Radiopharmaceutical Chemistry, German Cancer Research Center, Heidelberg, Germany, Department of Nuclear Medicine, Hospital of the Ludwig-Maximilians-University, Munich, Germany, Center of Molecular and Macromolecular Studies, Polish Academy of Science, Lodz, Poland, and Department of Inorganic Chemistry II, University of Dortmund, Dortmund, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology

Link

https://pubs.acs.org/doi/pdf/10.1021/bc700195y

Reference23 articles.

1. Towards molecular imaging and treatment of disease with radionuclides: the role of inorganic chemistry

2. Multimeric Cyclic RGD Peptides as Potential Tools for Tumor Targeting: Solid-Phase Peptide Synthesis and Chemoselective Oxime Ligation

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