A Convenient Synthesis of Vinyl Epoxides from Glycidic Esters via α-Hydroxy-β,γ-unsaturated Esters
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919308011126
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5. Oxyanionic substituent effect on the carbon-hydrogen insertion of carbenes. Reaction of alkoxides with dichlorocarbene and chlorophenylcarbene
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. HClO4·SiO2-mediated Improved Isomerization of Glycidic Esters to α-Hydroxy-β,γ-unsaturated Esters: Application in the Formal Synthesis of (R)-Baclofen and β-Phenyl GABA Analogues;Chemistry Letters;2012-03-05
2. ChemInform Abstract: A Convenient Synthesis of Vinyl Epoxides from Glycidic Esters via . alpha.-Hydroxy β,γ-Unsaturated Esters.;ChemInform;2010-08-18
3. Chemical reactions of spirooxiranes;Russian Journal of Organic Chemistry;2001
4. Asymmetric synthesis of chiral vinylic epoxides and α-hydroxy-β,γ-unsaturated esters via (−)-menthol based auxiliary and enzymatic resolution respectively;Tetrahedron: Asymmetry;1996-06
5. Reactions of 2-phenylthio-2-cycloalkenones and 2-[phenyl(thiomethyl)]-2-cycloalkenones: Synthesis of some useful chiral and achiral intermediates;Tetrahedron;1995-04
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