Strong deshielding in aromatic isoxazolines-Reference-Cited by-同舟云学术

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Strong deshielding in aromatic isoxazolines

Published:2015-09-14 Issue:1 Volume:54 Page:17-27
ISSN:0749-1581
Container-title:Magnetic Resonance in Chemistry
language:en
Short-container-title:Magn. Reson. Chem.

Author:

Ungvarská Maľučká Lucia¹,Vilková Mária¹,Kožíšek Jozef²,Imrich Ján¹

Affiliation:

1. P. J. Šafárik University, Faculty of Science; Institute of Chemistry, NMR Laboratory; Moyzesova 11 040 01 Košice Slovakia

2. Slovak Technical University, Faculty of Chemical and Food Technology; Department of Physical Chemistry; Radlinského 9 812 37 Bratislava Slovakia

Funder

Slovak Grant Agency VEGA

Slovak State NMR Program

Publisher

Wiley

Subject

General Materials Science,General Chemistry

Reference57 articles.

1. Regio- and stereochemistry of 1,3-dipolar cycloaddition of nitrile oxides to alkenes

2. Asymmetric 1,3-dipolar cycloadditions

3. Spiro Isoxazolines via Nitrile Oxide 1,3-Dipolar Cycloaddition Reactions

4. 1,3-Dipolar cycloaddition reactions on carbohydrate-based templates: synthesis of spiro-isoxazolines and 1,2,4-oxadiazoles as glycogen phosphorylase inhibitors

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1. Spectral Assignment in the [3 + 2] Cycloadditions of Methyl (2E)-3-(Acridin-4-yl)-prop-2-enoate and 4-[(E)-2-Phenylethenyl]acridin with Unstable Nitrile N-Oxides;Molecules;2024-06-09

2. Nitrile Oxide, Alkenes, Dipolar Cycloaddition, Isomerization and Metathesis Involved in the Syntheses of 2-Isoxazolines;Molecules;2023-03-10

3. Synthesis, spectral characterization, DNA binding ability and anti-cancer screening of new acridine-based derivatives;Medicinal Chemistry Research;2017-06-12

4. New spiroacridine derivatives with DNA-binding and topoisomerase I inhibition activity;Tetrahedron Letters;2016-12

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