Regie-Control of Formal [3 + 2] Cycloadditions of 5-Alkoxyoxazoles with Diethyl Oxomalonate
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/23/9/23_9_1673/_pdf
Reference6 articles.
1. Stereoselective synthesis of 2-oxazoline-4-carboxylates through Lewis acid-catalyzed formal [3+2] cycloadditions of 5-alkoxyoxazoles with aldehydes: catalytic effect of methylaluminum .beta.-binaphthoxide on cis-selectivity
2. Reactions of 5-alkoxyoxazoles with aldehydes in the presence of Lewis acid: regio- and stereoselective formation of 4-alkoxycarbonyl-2-oxazolines
3. Highly Diastereoselective Synthesis of 2-Oxazoline-4-carboxylates by Formal [3 + 2] Cycloadditions of a 5-Alkoxyoxazole with .alpha.-Alkoxy Aldehydes Catalyzed by Tin(IV) Chloride
4. Do oxazoliks undergo Diels-Alder reactions with heterodienophiles?
5. Reaction of thioaldehydes with 5-alkoxyoxazoles. A route to 3-thiazolines
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1. 5-Alkoxyoxazole - A Versatile Building Block in (Bio)organic Synthesis;European Journal of Organic Chemistry;2016-04-19
2. Catalytic Stereoselective Synthesis of Diverse Oxindoles and Spirooxindoles from Isatins;ACS Combinatorial Science;2012-04-02
3. Titanium-Catalyzed Stereoselective Synthesis of Spirooxindole Oxazolines;Organic Letters;2010-12-27
4. ChemInform Abstract: Regio-Control of Formal (3 + 2) Cycloadditions of 5-Alkoxyoxazoles with Diethyl Oxomalonate.;ChemInform;2010-08-18
5. Compendium of Cycloaddition Reactions under High Pressure;Helvetica Chimica Acta;2005-08
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