A “Click Chemistry” Approach to the Efficient Synthesis of Multiple Imaging Probes Derived from a Single Precursor-Reference-Cited by-同舟云学术

A “Click Chemistry” Approach to the Efficient Synthesis of Multiple Imaging Probes Derived from a Single Precursor

Published:2009-10-05 Issue:10 Volume:20 Page:1940-1949
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Mindt Thomas L.¹,Müller Cristina¹,Stuker Florian¹,Salazar Jean-Frédéric¹,Hohn Alexander¹,Mueggler Thomas¹,Rudin Markus¹,Schibli Roger¹

Affiliation:

1. Department of Chemistry and Applied Biosciences, ETH Zurich, Center for Radiopharmaceutical Science ETH-PSI-USZ, Paul Scherrer Institute, Villigen, Institute for Biomedical Engineering and Institute of Pharmacology and Toxicology, University and ETH Zurich, Switzerland

Publisher

American Chemical Society (ACS)

Subject

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

Link

https://pubs.acs.org/doi/pdf/10.1021/bc900276b

Reference51 articles.

1. Molecular Imaging with PET

2. Molecular imaging in drug discovery and development

3. Molecular imaging in drug development

4. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes

5. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

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