Efficient Regioselective Ring Opening of Activated Aziridine-2-Carboxylates with [18 F]Fluoride-Reference-Cited by-同舟云学术

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Efficient Regioselective Ring Opening of Activated Aziridine-2-Carboxylates with [18 F]Fluoride

Published:2014-11-21 Issue:1 Volume:4 Page:65-71
ISSN:2191-1363
Container-title:ChemistryOpen
language:en
Short-container-title:ChemistryOpen

Author:

Schjoeth-Eskesen Christina,Hansen Paul Robert,Kjaer Andreas,Gillings Nic

Funder

Danish Research Council

Novo Nordisk Foundation

Lundbeck Foundation

Svend Andersen Foundation

Innovationsfonden

Director Michael Hermann Nielsen Memorial Fund

Else and Mogens Wedell-Wedellsborg Foundation

John and Birthe Meyer Foundation

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/open.201402081/fullpdf

Reference40 articles.

1. Versatile use of acid-catalyzed ring-opening of β-aziridinyl-α,β-enoates to stereoselective synthesis of peptidomimetics

2. Recent developments in regioselective ring opening of aziridines

3. Ring Opening of a Resin-Bound Chiral Aziridine with Phenol Nucleophiles

4. Regiospecific and Enantiospecific Ring Opening of Methyl (+)-(1'R, 2R)- and (-)-(1'R, 2S)-1-(2-phenylethanol) Aziridine-2-carboxylates

5. Substituents Effect on Aziridine Chemistry: N-Inversion Energy, Reactivity and Regioselectivity of Nucleophilic Ring-opening

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1. Synthesis of Optically Active Organofluorides by Ring Opening of Oxazolidinone-Fused Aziridines;Organic Letters;2022-12-28

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3. Methods to Enhance the Metabolic Stability of Peptide-Based PET Radiopharmaceuticals;Molecules;2020-05-14

4. A fully automated azeotropic drying free synthesis of O-(2-[18F]fluoroethyl)- -tyrosine ([18F]FET) using tetrabutylammonium tosylate;Applied Radiation and Isotopes;2019-10

5. Deoxyradiofluorination Reaction from β-Hydroxy-α-aminoesters: an Entry to [18 F]Fluoroaminoesters under Mild Conditions;European Journal of Organic Chemistry;2019-06-06

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