Use of palladium-mediated allylic substitution reactions in the synthesis of 2,5-disubstituted-2,5-dihydrofurans
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Enantioselective palladium catalyzed allylic substitution with a new phosphite ligand issued from (2S,5S)-hexanediol
2. Palladium-catalysed substitution reactions of geminal allylic diacetates
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4. Allylic Amination
5. Ruthenium tetraoxide: a mild reagent for the oxidation of 2′,3′-O-isopropylidene purine nucleosides
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1. Towards a better understanding of the electrosynthesis of 2,5-dicarboxy-2,5-dihydrofurans: structure, mechanism and influence over stereochemistry;Royal Society Open Science;2019-07
2. Regioselective vicinal functionalization of unactivated alkenes with sulfonium iodate(i) reagents under metal-free conditions;Organic & Biomolecular Chemistry;2016
3. 1,3-Dioxins, Oxathiins, Dithiins, and their Benzo Derivatives;Comprehensive Heterocyclic Chemistry III;2008
4. Transition metals in organic synthesis: Highlights for the year 2004;Coordination Chemistry Reviews;2006-10
5. Use of Palladium-Mediated Allylic Substitution Reactions in the Synthesis of 2,5-Disubstituted-2,5-dihydrofurans.;ChemInform;2005-01-18
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