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Organic Letters, ISSN 1523-7060, 11/2018, Volume 20, Issue 21, pp. 6882 - 6885
The first catalytic asymmetric conjugate addition to γ,δ-unsaturated β-dicarbonyl compounds was developed. With a chiral diene–rhodium­(I) μ-chloro dimer as... 
MULTICOMPONENT REACTIONS | CROSS-COUPLING REACTIONS | ENANTIOSELECTIVE ALLYLIC SUBSTITUTION | 1,4-ADDITION REACTIONS | CHIRAL DIENE LIGANDS | 1,3-DICARBONYL COMPOUNDS | QUATERNARY STEREOCENTERS | CHEMISTRY, ORGANIC | STEREOSELECTIVE-SYNTHESIS | ARYLBORONIC ACIDS | ALPHA,BETA-UNSATURATED CARBONYL
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
Angewandte Chemie-International Edition, ISSN 1433-7851, 2011, Volume 50, Issue 26, pp. 5834 - 5838
Naphthol compounds bearing a pendant α,β‐unsaturated ester undergo a copper(I)‐catalyzed asymmetric conjugate addition/copper(II)‐mediated intramolecular... 
dearomatization | oxidation | CARBONYL-COMPOUNDS | DIMERIZATION | asymmetric catalysis | ENANTIOSELECTIVE OXIDATIVE DEAROMATIZATION | conjugate addition | spiro compounds | PHENOLS | STEREOCENTERS | DIVERSITY | ALPHA,BETA-UNSATURATED ESTERS | DERIVATIVES | GRIGNARD-REAGENTS | ACCESS | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2006, Volume 45, Issue 30, pp. 4966 - 4970
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 05/2016, Volume 138, Issue 17, pp. 5623 - 5633
The first copper-catalyzed direct β-functionalization of saturated ketones is reported. This protocol enables diverse ketones to couple with a wide range of... 
ELECTRON-TRANSFER OXIDATION | H FUNCTIONALIZATION | C(SP)-H BOND ACTIVATION | AEROBIC ALCOHOL OXIDATION | QUATERNARY STEREOCENTERS | ALPHA,BETA-UNSATURATED CARBONYL-COMPOUNDS | ALPHA-AMINO-ACIDS | STEREOSELECTIVE-SYNTHESIS | RADICAL-ADDITION | CHEMISTRY, MULTIDISCIPLINARY | METAL-FREE
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2010, Volume 49, Issue 7, pp. 1194 - 1196
Learn your ABCs! The asymmetric borylation in conjugate fashion has rapidly progressed in recent years if not months (see scheme, pin=pinacolato, TM=transition... 
copper | asymmetric catalysis | boron | conjugate addition | main group chemistry | Conjugate addition | Boron | Main group chemistry | Copper | Asymmetric catalysis | ALPHA,BETA-UNSATURATED CARBONYL-COMPOUNDS | ORGANOBORONIC ESTERS | CATALYST | TERTIARY | CHEMISTRY, MULTIDISCIPLINARY | BETA-BORATION | COUPLING REACTIONS | ENONES
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 05/2017, Volume 56, Issue 22, pp. 6268 - 6271
Journal Article
Chemical Communications, ISSN 1359-7345, 2009, Issue 43, pp. 6577 - 6579
The highly enantioselective conjugate boration of six-membered and seven-membered cyclic enones and unsaturated esters was achieved by the use of a... 
1,4-DIBORATION | ALPHA,BETA-EPOXY KETONES | BORATION | ASYMMETRIC-SYNTHESIS | REDUCTION | BIS(PINACOLATO)DIBORON | EFFICIENT SYNTHESIS | DIBORON REAGENTS | ALPHA,BETA-UNSATURATED ESTERS | CHEMISTRY, MULTIDISCIPLINARY | AMIDES
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 08/2009, Volume 131, Issue 33, pp. 11664 - 11665
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 09/2015, Volume 357, Issue 13, pp. 2745 - 2780
Journal Article