New modification of the Perkow reaction: halocarboxylate anions as leaving groups in 3-acyloxyquinoline-2,4(1H,3H)-dione compounds
Author:
Publisher
Beilstein Institut
Subject
Organic Chemistry
Link
https://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-1-17.pdf
Reference17 articles.
1. Synthesen von 3-Hydroxy-tetrahydrochinolin-2.4-dionen Syntheses of 3-Hydroxy-tetrahydroquinoline-2,4-diones
2. Synthetic approaches to butenolides
3. Conversion of 3-hydroxy-1,2,3,4-tetrahydroquinoline-2,4-diones to 2,3a,4,5-tetrahydrofuro[2,3-c]quinoline-2,4-dionesviaan intramolecular wittig reaction
4. The Chemistry and Properties of Enol Phosphates.
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1. Synthesis of enol phosphates directly from ketones via a modified one-pot Perkow reaction;RSC Advances;2022
2. Chemistry and Applications of 4-Hydroxyquinolin-2-one and Quinoline-2,4-dionebased Compounds;Current Organic Chemistry;2017-10-09
3. Nef–Perkow–Mumm Cascade towards Imido Phosphate Derivatives;Synlett;2017-08-11
4. Synthesis of 1,2-dihydro-2-oxo-4-quinolinyl phosphates from 2-acyl-benzoic acids;Tetrahedron Letters;2015-03
5. A simple and efficient synthesis of [2H10]deuterated bromfenvinphos by the Perkow reaction;Journal of Labelled Compounds and Radiopharmaceuticals;2011-06-03
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