Chemoselective reduction of an α,β-epoxy ketone moiety coexisting with an enone function
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Organoselenium-mediated reduction of α,β-epoxy ketones to β-hydroxy ketones: A new access to inter- and intramolecular aldols
2. Organoselenium-mediated Reduction of α, β-Epoxy Esters to β-Hydroxy Esters
3. Sodium phenylseleno(triethoxy)borate, Na+(PhSeB(OEt)3]−: The reactive species generated from (PhSe)2 with NaBH4 in ethanol
4. Mild procedure for the conversion of epoxides to allylic alcohols. First organoselenium reagent
5. Reduction of .alpha.,.beta.-oxido ketones with chromous acetate. Synthesis of 3.beta.,5.beta.,17.beta.,19-tetrahydroxy-5.beta.-androstane, a degradation product of strophanthidin
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1. Formation of Alcohols and Phenols by Ether Cleavage;Comprehensive Organic Transformations;2018-02-28
2. Synthesis of Epoxyisoprostanes: Effects in Reducing Secretion of Pro-inflammatory Cytokines IL-6 and IL-12;Angewandte Chemie International Edition;2013-04-16
3. Synthese von Epoxyisoprostanen: verminderte Sekretion der entzündungsfördernden Zytokine IL-6 und IL-12;Angewandte Chemie;2013-04-16
4. Methods and mechanisms of epoxy compounds reduction;Russian Journal of Organic Chemistry;2008-02
5. Selective reduction of α,β-epoxyketones to β-hydroxyketones using silyllithium reagents;Tetrahedron Letters;2007-09
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