Synthesis of 18F-labeled Neurotensin(8-13) via Copper-Mediated 1,3-Dipolar [3+2]Cycloaddition Reaction
Article Properties
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LanguageEnglish
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DOI (url)
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Publication Date2007/06/01
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Indian UGC (journal)
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Citations33
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Theres Ramenda
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Ralf Bergmann
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Frank Wuest
Cite
Ramenda, Theres, et al. “Synthesis of 18F-Labeled Neurotensin(8-13) via Copper-Mediated 1,3-Dipolar [3+2]Cycloaddition Reaction”. Letters in Drug Design &Amp; Discovery, vol. 4, no. 4, 2007, pp. 279-85, https://doi.org/10.2174/157018007784619998.
Ramenda, T., Bergmann, R., & Wuest, F. (2007). Synthesis of 18F-labeled Neurotensin(8-13) via Copper-Mediated 1,3-Dipolar [3+2]Cycloaddition Reaction. Letters in Drug Design &Amp; Discovery, 4(4), 279-285. https://doi.org/10.2174/157018007784619998
Ramenda, Theres, Ralf Bergmann, and Frank Wuest. “Synthesis of 18F-Labeled Neurotensin(8-13) via Copper-Mediated 1,3-Dipolar [3+2]Cycloaddition Reaction”. Letters in Drug Design &Amp; Discovery 4, no. 4 (2007): 279-85. https://doi.org/10.2174/157018007784619998.
Ramenda T, Bergmann R, Wuest F. Synthesis of 18F-labeled Neurotensin(8-13) via Copper-Mediated 1,3-Dipolar [3+2]Cycloaddition Reaction. Letters in Drug Design & Discovery. 2007;4(4):279-85.
Journal Categories
Medicine
Public aspects of medicine
Toxicology
Poisons
Medicine
Therapeutics
Pharmacology
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Citations
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
| Recent Advances in Bioorthogonal Click Chemistry for Enhanced PET and SPECT Radiochemistry | Bioconjugate Chemistry |
| 11 | 2023 |
Radiosynthesis of 5-[18F]Fluoro-1,2,3-triazoles through Aqueous Iodine–[18F]Fluorine Exchange Reaction | Molecules |
| 2 | 2021 |
A Compact and Synthetically Accessible Fluorine‐18 Labelled Cyclooctyne Prosthetic Group for Labelling of Biomolecules by Copper‐Free Click Chemistry | ChemMedChem |
| 10 | 2018 |
18F‐Labeling of Sensitive Biomolecules for Positron Emission Tomography | Chemistry – A European Journal |
| 66 | 2017 |
| Small Prosthetic Groups in 18 F-Radiochemistry: Useful Auxiliaries for the Design of 18 F-PET Tracers | Seminars in Nuclear Medicine |
| 34 | 2017 |
Citations Analysis
The category
Science: Chemistry 23
is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled Radiosynthesis and bioconjugation of [18F]FPy5yne, a prosthetic group for the 18F labeling of bioactive peptides and was published in 2008. The most recent citation comes from a 2023 study titled Recent Advances in Bioorthogonal Click Chemistry for Enhanced PET and SPECT Radiochemistry. This article reached its peak citation in 2009, with 5 citations. It has been cited in 19 different journals, 15% of which are open access. Among related journals, the Journal of Labelled Compounds and Radiopharmaceuticals cited this research the most, with 4 citations. The chart below illustrates the annual citation trends for this article.