How to increase the reactivity of [18F]fluoroethyl bromide: [18F]fluoroethylation of amine, phenol and amide functional groups with [18F]FEtBr, [18F]FEtBr/NaI and [18F]FEtOTf-Reference-Cited by-同舟云学术

How to increase the reactivity of [18F]fluoroethyl bromide: [18F]fluoroethylation of amine, phenol and amide functional groups with [18F]FEtBr, [18F]FEtBr/NaI and [18F]FEtOTf

Published:2003 Issue:6 Volume:46 Page:587-598
ISSN:0362-4803
Container-title:Journal of Labelled Compounds and Radiopharmaceuticals
language:en
Short-container-title:J. Labelled Cpd. Radiopharm.

Author:

Zhang Ming-Rong,Furutsuka Kenji,Yoshida Yuichiro,Suzuki Kazutoshi

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Radiology Nuclear Medicine and imaging,Biochemistry,Analytical Chemistry

Reference18 articles.

1. A rapid and efficient method for the fluoroalkylation of amines and amides. Development of a method suitable for incorporation of the short-lived positron emitting radionuclide fluorine-18

2. Synthesis of two radiofluorinated cocaine analogues using distilled 2-[18F]fluoroethyl bromide

3. Radiosynthesis and biodistribution of the S-[18F]fluoroethyl analog of McN5652

4. Synthesis of no-carrier-added N-([18F]fluoroalkyl)spiperone derivatives

5. Syntheses and D2 receptor affinities of derivatives of spiperone containing aliphatic halogens

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