One-pot vinylogous aldol addition of β,γ-unsaturated esters under mild conditions
Author:
Affiliation:
1. Department of Chemistry
2. Faculty of Science
3. İzmir Institute of Technology
4. Urla 35430
5. Turkey
Abstract
A new methodology for the addition of β,γ-unsaturated esters to aldehydes was developed in a TMSCl, Ag2CO3, and TBAF mixture.
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2015/NJ/C5NJ00961H
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3. Synthesis of α,β-Unsaturated δ-Lactones by Vinyl Acetate Mediated Asymmetric Cross-Aldol Reaction of Acetaldehyde: Mechanistic Insights
4. Trienediolates of hexadienoic acids in synthesis. Addition to unsaturated ketones. A convergent approach to the synthesis of retinoic acids
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1. Novel 2′-alkoxymethyl substituted klavuzon derivatives as inhibitors of Topo I and CRM1;Bioorganic Chemistry;2020-10
2. 1,5,7-Triazabicylodec-5-ene-Promoted Direct Vinylogous Aldol Reaction for the Synthesis of 3-Hydroxy-2-oxoindole Derivatives;Synlett;2019-02-11
3. Enzyme mediated kinetic resolution of δ-hydroxy-α,β-unsaturated esters as a route to optically active δ-lactones;Tetrahedron: Asymmetry;2017-06
4. ChemInform Abstract: One-Pot Vinylogous Aldol Addition of β,γ-Unsaturated Esters under Mild Conditions.;ChemInform;2015-10-22
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