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European Journal of Organic Chemistry, ISSN 1434-193X, 09/2019, Volume 2019, Issue 33, pp. 5624 - 5635
Preparation of 2,2‐disubstituted and 2‐monosubstituted alkenylboronic acid esters from aliphatic and aromatic ketones and aldehydes by the boron‐Wittig... 
Boron‐Wittig olefination | Boronic esters | Alkenes | Organoboron compounds | Boron-Wittig olefination | HYDROBORATION | DIVERSIFICATION | ESTERS | CHEMISTRY, ORGANIC | CARBANIONS | ALKYNES | BORYLATION | Methane | Ketones | Aldehydes
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2018, Volume 2018, Issue 15, pp. 1774 - 1784
Carbanions of sulfonyl halides and activated sulfonates add to carbonyl compounds, and so‐formed aldol‐type adducts spontaneously fragment into olefins. This... 
Carbanions | Sulfonates | Selectivity | Alkenes | Olefination | REAGENTS | STEREOCHEMISTRY | WITTIG OLEFINATION | CHEMISTRY, ORGANIC | CARBONYL-COMPOUNDS | ALDEHYDES | FLUORIDE | DIELS-ALDER REACTION | STEREOSELECTIVE-SYNTHESIS | PETERSON OLEFINATIONS | WATER | Halides | Olefins | Organic compounds
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 02/2017, Volume 2017, Issue 8, pp. 1184 - 1190
A very simple and efficient diastereoselective synthesis of 1,2‐disubstituted alkenes has been achieved under mild conditions. Sulfoxide stabilised N... 
Phosphorus | Sulfinylimines | Wittig reactions | Alkenes | Olefination | Diastereoselectivity | SAMARIUM DIIODIDE | CROSS-METATHESIS | ASYMMETRIC-SYNTHESIS | CHEMISTRY, ORGANIC | HECK REACTIONS | ALDEHYDES | PHOSPHONATE CARBANIONS | ALKYNES | TERT-BUTANESULFINYL IMINES | C-H ALKENYLATION | SUZUKI REACTIONS | Phosphonates
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 08/2018, Volume 24, Issue 43, pp. 11110 - 11118
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2014, Volume 53, Issue 41, pp. 11092 - 11095
Journal Article
Catalysis Letters, ISSN 1011-372X, 3/2017, Volume 147, Issue 3, pp. 693 - 703
Five different Ru metal precursors were reduced in imidazolium based ionic liquids under hydrogen atmosphere (4 bar) at 50 °C to obtain well-dispersed and... 
Chemistry | Stilbenes | Physical Chemistry | Organometallic Chemistry | Resveratrol | Wittig type olefination reaction | Catalysis | Industrial Chemistry/Chemical Engineering | DMU-212 | Ru nanoparticle | OXIDATION | ALCOHOLS | HYDROGENATION | MECHANISM | CHEMISTRY | CHEMISTRY, PHYSICAL | IONIC LIQUIDS | Nanoparticles | Usage | Ruthenium | Hydrogen | Analysis | Solvents | Transmission electron microscopy | Ionic liquids | Ions | Selectivity
Journal Article
Organic Letters, ISSN 1523-7060, 07/2011, Volume 13, Issue 13, pp. 3418 - 3421
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 11/2015, Volume 2015, Issue 33, pp. 7259 - 7263
Journal Article
Catalysis Communications, ISSN 1566-7367, 08/2014, Volume 53, pp. 87 - 90
New self-assembled phosphorus ligands are synthesized and used in the rhodium complex catalyzed hydroformylation–Wittig reaction of homoallylic olefins under... 
Hydroformylation–Wittig reaction | Oxa-Michael reaction | Phosphorus self-assembling ligand | Homoallylic olefin | β-Pyran | Wittig reagent | Hydroformylation-Wittig reaction | beta-Pyran | ENANTIOSELECTIVE HYDROGENATION | CONSTRUCTION | CHEMISTRY, PHYSICAL | HOMOGENEOUS CATALYSIS | REACTION SEQUENCES
Journal Article
by Gu, YH and Tian, SK
2012, Topics in Current Chemistry, Volume 327, 42
A range of phosphorus-stabilized carbon nucleophiles have been employed for alkene synthesis with high chemo-, regio-, and stereoselectivity. The Wittig,... 
PHOSPHINOXYDE ALS OLEFINIERUNGSREAGENZIEN | ARYL ALKYL KETONES | Alkenes | Ketones | ONE-POT | CHEMISTRY, ORGANIC | Phosphorus | Aldehydes | P-31 NMR-SPECTROSCOPY | WADSWORTH-EMMONS REACTION | Z-UNSATURATED ESTERS | Imines | PORPHYRIN-CATALYZED OLEFINATION | AQUEOUS WITTIG REACTIONS | Z-SELECTIVE SYNTHESIS | DOUBLE-BOND FORMATION
Book Chapter
Angewandte Chemie - International Edition, ISSN 1433-7851, 01/2013, Volume 52, Issue 5, pp. 1564 - 1567
Journal Article
ChemCatChem, ISSN 1867-3880, 01/2014, Volume 6, Issue 1, pp. 131 - 134
Cuprous iodide‐catalyzed Wittig olefination reactions of N ‐tosylhydrazones with trifluoromethylketones are reported. This procedure provides an efficient... 
tosylhydrazones | Wittig reaction | copper | alkenes | diazo compounds | trifluoromethylketones | SELECTIVE OLEFINATION | CHEMISTRY, PHYSICAL | CARBONYL-COMPOUNDS | PHOSPHORUS YLIDES | ETHYL DIAZOACETATE | MEDICINAL CHEMISTRY | PORPHYRIN-CATALYZED OLEFINATION | ALDEHYDE-OLEFINATION | STEREOSELECTIVE-SYNTHESIS | EPOXIDATION-ISOMERIZATION | TERMINAL ALKENES | Copper | Diazo compounds
Journal Article
ChemCatChem, ISSN 1867-3880, 05/2016, Volume 8, Issue 9, pp. 1636 - 1640
The Wittig‐type carbonyl olefination reaction has no biocatalytic equivalent. To build complex molecular scaffolds, however, C−C bond‐forming reactions are... 
C−C bond formation | enzyme catalysis | Wittig reactions | biocatalysis | olefination | C-C bond formation | COMPLEX | CHEMISTRY, PHYSICAL | ALDEHYDES | SQUALENE HOPENE CYCLASES | EFFICIENT | Enzymes | Catalysis | Aldehydes | Escherichia coli | Heme
Journal Article