Oxidative ring opening of furan derivatives to α,β-unsaturated γ-dicarbonyl compounds, useful intermediates for 3-oxocyclopentenes synthesis
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. The oxidation of furan derivatives with pyridinium chlorochromate: A novel synthesis of 6-hydroxy-2 h-pyran-3 (6 H)-ones
2. Pyridinium chlorochromate in the organic synthesis: a convenient oxidation of 5-bromo-2-furan-derivatives to γ-hydroxy butenolides
3. Pyridinium chlorochromate. An efficient reagent for oxidation of primary and secondary alcohols to carbonyl compounds
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1. The Synthesis of Trans-enediones from Furan Derivatives using Pyridinium Chlorochromate: An Explanation;Current Organic Chemistry;2024-09
2. Dess–Martin Periodinane/Brønsted Acid-Mediated Tandem Oxidation/Cyclization of Homopropargylic Alcohols for Synthesis of Trisubstituted Furans;Synlett;2023-03-06
3. General Method for the Synthesis of Substituted Cyclopentenones via α-Borylzirconacyclopentene Intermediates;Organic Preparations and Procedures International;2020-01-02
4. Oxidative ring-opening of benzothiazole derivatives;Canadian Journal of Chemistry;2019-05
5. Total Synthesis of (−)‐Cephalotaxine and (−)‐Homoharringtonine via Furan Oxidation–Transannular Mannich Cyclization;Angewandte Chemie International Edition;2019-04-04
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