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Tetrahedron Letters, ISSN 0040-4039, 08/2019, Volume 60, Issue 32, p. 150906
A metal-free and two-phase protocol for the Meyer-Schuster isomerization of propargyl alcohols to the corresponding α,β-unsaturated carbonyl compounds has been... 
Meyer-Schuster rearrangement | H3PO3 aqueous solution | Two-phase | α,β-Unsaturated carbonyl compounds | REARRANGEMENT | OLEFINATION | MECHANISM | CHEMISTRY, ORGANIC | ALDEHYDES | alpha,beta-Unsaturated carbonyl compounds
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 12/2019, Volume 183, p. 111687
Conjugated α,β-unsaturated ketones are very useful compounds associated with diverse medicinal properties. This review outlines α,β-unsaturated ketones as... 
Cytotoxins | Mitochondria | Chalcones | α,β-unsaturated ketones | Curcumin | Structure-activity relationships | Tumors
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 04/2019, Volume 361, Issue 7, pp. 1554 - 1558
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 05/2015, Volume 2015, Issue 14, pp. 3044 - 3047
In this study, we developed a general iron‐catalyzed α‐methylenation of ketones by using N,N‐dimethylacetamide as the one‐carbon source. Various ketones,... 
Methylenation | CDC reaction | One‐carbon source | α, β‐unsaturated carbonyls | Iron‐catalysis | Iron-catalysis | α, β-unsaturated carbonyls | One-carbon source | OXIDATION | alpha, beta-unsaturated carbonyls | ACTIVATION | ACID | ALKYLATION | BAYLIS-HILLMAN REACTION | CHEMISTRY, ORGANIC | ADJACENT | FUNCTIONALIZATION | AMINES | C-C BOND
Journal Article
Catalysis Communications, ISSN 1566-7367, 05/2017, Volume 94, pp. 23 - 28
The hydrosilylation of aldehydes and ketones under mild conditions with hydrido thiophenolato iron(II) complexes [ –Fe(H)(SAr)(PMe ) ] ( ) as catalysts is... 
Hydrosilylation | Iron hydride | Silane | α,β-Unsaturated carbonyl compound | Carbonyl compound | DIHYDRIDE | REACTIVITY | CHEMISTRY, PHYSICAL | ALDEHYDES | H BOND ACTIVATION | KETONES | LIGANDS | EFFICIENT HYDROSILYLATION | BEARING | alpha,beta-Unsaturated carbonyl compound | COBALT | Ketones | Aldehydes | Fine chemicals
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 01/2013, Volume 19, Issue 2, pp. 601 - 605
NCN‐pincer Ru‐complexes containing bis(oxazolinyl)phenyl ligands serve as suitable catalysts in the direct conjugate additions of α,β‐unsaturated carbonyl... 
ruthenium | α,β‐unsaturated compounds | conjugate addition | alkynes | pincer complex | α,β- unsaturated compounds | DIARYLPHOSPHINES | ACTIVATION | alpha,beta-unsaturated compounds | TERMINAL ALKYNES | ASYMMETRIC ADDITION | ANTI-MARKOVNIKOV-ADDITION | ALKYNYLATION | SILYLACETYLENES | CHEMISTRY, MULTIDISCIPLINARY | LIGANDS | 1,4-ADDITION
Journal Article
Tetrahedron, ISSN 0040-4020, 02/2015, Volume 71, Issue 7, pp. 1132 - 1135
An operationally simple and environmentally benign catalytic procedure has been developed to selectively reduce different α,β-unsaturated ketones. The... 
α,β-unsaturated carbonyl | 2-MeTHF | Green chemistry | Luche reduction | Er (III) triflate | α β-unsaturated carbonyl
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 06/2016, Volume 57, Issue 24, pp. 2587 - 2590
Ligand-free CuI-catalyzed bis(pinacolato)diboron (B (pin) ) conjugate addition and reduction onto α,β-unsaturated carbonyl compounds in moderate to excellent... 
Conjugate addition | Reduction | α,β-Unsaturated carbonyl compounds | Bis(pinacolato)diboron | Ligand-free | CARBENE | ENANTIOSELECTIVE BETA-BORATION | CHEMISTRY, ORGANIC | TERTIARY | ALKENES | LIGANDS | ESTERS | DIBORATION | alpha,beta-Unsaturated carbonyl compounds | AMIDES
Journal Article