A New Synthetic Method for α-Oxo-β,γ-unsaturated Esters
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/65/11/65_11_3209/_pdf
Reference10 articles.
1. Accelerated inverse electron demand Diels-Alder reactions of 1-oxa-1,3-butadienes: [4 + 2] cycloaddition reactions of .beta.,.gamma.-unsaturated .alpha.-keto esters
2. Divergent de novo synthesis of carbohydrates based on an accelerated inverse electron demand Diels-Alder reaction of 1-oxa-1,3-butadienes
3. Hetero-Diels-Alder Reaction of Substituted 1-Oxabutadienes and 2-Ethoxyvinylacetate An entry to various natural occurring carbohydrates
4. 2-oxo-3-butenoate esters as dienophiles and their utility in a novel synthesis of pyrroles
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1. Iodine mediated a simple strategy for the synthesis of β,γ-unsaturated-α-ketoesters and its application for the synthesis of 4,5-dihydropyrazole derivatives;Journal of the Iranian Chemical Society;2020-02-27
2. Dihydropyrans by Cycloadditions of Oxadienes;Organic Reactions;2020-01-09
3. Direct Synthesis of β,γ-Unsaturated α-Keto Esters from Aldehydes and Pyruvates;Synlett;2019-02-25
4. Stereoselective access to (Z)-α,γ-diazido-α,β-unsaturated esters via Lewis acid-mediated 1,3-diazidation of α,α-dimethoxy-β,γ-unsaturated esters with trimethylsilyl azide;Tetrahedron Letters;2015-05
5. Synthesis in ionic liquids only: access to α-oxo-γ-thio-esters via Mukaiyama coupling;Tetrahedron Letters;2014-02
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