LG
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Copper-Catalyzed Enantioselective Conjugate Addition to α,β-Unsaturated Aldehydes with Various Organometallic Reagents | Synthesis | 2016 | 686 | 2 | |||
| Construction of Bicyclo[3.2.1]octanes with Four Stereogenic Centers by Organocatalytic Domino Michael/Aldol Reaction | Organic letters | 2014 | 659 | 0 | |||
| Enantioselective Copper-Catalyzed Conjugate Addition of Trimethylaluminum to β,γ-Unsaturated α-Ketoamides: Efficient Access to γ-Methyl-Substituted Carbonyl Compounds | Angewandte Chemie | 2013 | 715 | 4 | |||
| Copper-catalyzed Asymmetric Conjugate Addition to Challenging Michael Acceptors and Synthesis of Relevant Target Molecules | Chimia | 2012 | 634 | 0 | |||
| Enantioselective Copper-Catalyzed Conjugate Addition of Trimethylaluminium to β,γ-Unsaturated α-Ketoesters | Angewandte Chemie | 2012 | 751 | 0 | |||
| Enantioselective copper-catalyzed conjugate addition to sensitive Michael acceptors and application to natural product synthesis use in perfumes and flavours chemistry | 2012 | 1,173 | 6 | ||||
| Copper-catalysed kinetic resolution of cyclic alkenyl cyclopropane malonates with organoaluminium and Grignard reagents | Synlett | 2010 | 696 | 0 | |||
| Rhodium-Catalyzed Asymmetric 1,4-Addition of Aryl Alanes to Trisubstituted Enones: Binap as an Effective Ligand in the Formation of Quaternary Stereocenters | Angewandte Chemie | 2010 | 782 | 0 | |||
| Copper catalysed asymmetric ring opening reaction of oxabenzonorbornadienes with grignard and aluminium reaggents | Synthesis | 2009 | 628 | 0 | |||
| Analysis of amphetamine derivatives in plasma using capillary zone electrophoresis coupled with laser-induced fluorescence after derivatization on solid-phase extraction support | Chimia | 2008 | 547 | 0 | |||
| Screening of π-Basic Naphthalene and Anthracene Amplifiers for π-Acidic Synthetic Pore Sensors | Journal of the American Chemical Society | 2008 | 671 | 0 | |||
| Control of Redox Potential by Deprotonation of Coordinated 1H-Imidazole in Complexes of 2-(1H-Imidazol-2-yl)pyridine | Helvetica Chimica Acta | 2005 | 352 | 0 |
