4.2.3.7. Synthesis of a Biologically Active Oxazol-5(4<i>H</i>)-One <i>via</i> Erlenmeyer

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4.2.3.7. Synthesis of a Biologically Active Oxazol-5(4H)-One via Erlenmeyer–Plöchl Reaction

Published:2016-12-16 Issue: Volume: Page:391-395
ISSN:
Container-title:Comprehensive Organic Chemistry Experiments for the Laboratory Classroom
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Author:

Rodrigues Catarina A. B.¹,Martinho José M. G.²,Afonso Carlos A. M.¹

Affiliation:

1. Instituto de Investigação do Medicamento (iMed.ULisboa), Faculty of Pharmacy, University of Lisbon Av. Prof. Gama Pinto 1649-003 Lisboa Portugal catarinarodrigues@ff.ulisboa.pt carlosafonso@ff.ulisboa.pt

2. Centro de Química-Física Molecular and IN-Institute of Nanoscience and Nanothecnology, Instituto Superior Técnico Av. Rovisco Pais 1049-001 Lisboa Portugal

Publisher

The Royal Society of Chemistry

Link

https://books.rsc.org/books/edited-volume/chapter-pdf/1686299/bk9781849739634-00391.pdf

Reference27 articles.

1. The diverse chemistry of oxazol-5-(4H)-ones

2. Stereoselective syntheses of quaternary substituted α-amino acids using oxazol-5-(4H)-ones

3. Oxazolones in Organocatalysis, New Tricks for an Old Reagent

4. Two-photon absorption properties of push–pull oxazolones derivatives

5. Syntheses of Highly Fluorescent GFP-Chromophore Analogues

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