Stereospecific radiosynthesis of 3-fluoro amino acids: access to enantiomerically pure radioligands for positron emission tomography-Reference-Cited by-同舟云学术

Stereospecific radiosynthesis of 3-fluoro amino acids: access to enantiomerically pure radioligands for positron emission tomography

Published:2018 Issue:13 Volume:16 Page:2219-2224
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Alluri Santosh R.¹²³⁴⁵,Riss Patrick J.¹²³⁴⁵^ORCID

Affiliation:

1. Realomics Strategic Research Initiative

2. Department of Chemistry

3. University of Oslo

4. Oslo

5. Norway

Abstract

A variety of substituted non-racemic aziridine-2-carboxylates equivalent to amino acids were prepared and subjected to ring opening reaction by [¹⁸F/¹⁹F]fluoride.

Funder

Universitetet i Oslo

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB00184G

Reference25 articles.

1. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations

2. Synthesis and ring openings of cinnamate-derived N-unfunctionalised aziridines

3. Development of PET and SPECT Probes for Glutamate Receptors

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