A new route to α,β-unsaturated aldehydes using the condensation of trimethylsilyl β-trimethylsilyl enol ethers with aldehydes.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Michael-type addition of O-ethyl-C,O-bis(trimethylsilyl)ketene acetal and its application to the synthesis of α-ylidene-δ-lactones
2. Stereoselective synthesis of (E)- α, β -unsaturated acids from C,O,O-tri (trimethylsilyl) ketene acetal and aldehydes.
3. Synthese von 5-Arylmethylen-1,3-dioxolan-4-onen und β-Aryl-α-ketocarbonsäuren
4. Pyrolytic rearrangements of α,β-epoxysilanes to silyl enol ethers
5. Aldéhydes α-silylés: préparation et propriétés nouvelles
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1. Synthesis of α,β-Unsaturated Aldehydes with an (E)-Trisubstituted Double Bond via Ring Opening of Cyclopropanols;Russian Journal of Organic Chemistry;2021-10
2. A simple Hückel model-driven strategy to overcome electronic barriers to retro-Brook silylation relevant to aryne and bisaryne precursor synthesis;Chemical Communications;2021
3. Electrochemical Formation of Cinnamaldehyde by the Electrolyte System N,N ‐Diisopropylethylamine and 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol;ChemElectroChem;2020-04
4. Formation of Aldehydes and Ketones by Carbonyl Homologation;Comprehensive Organic Transformations;2018-02-28
5. ChemInform Abstract: A new Route to α,β-Unsaturated Aldehydes Using the Condensation of Trimethylsilyl β-Trimethylsilyl Enol Ethers with Aldehydes.;ChemInform;2010-08-19
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