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International Journal of Biological Macromolecules, ISSN 0141-8130, 07/2018, Volume 113, pp. 711 - 718
Owe to unique advantages of heterogeneous catalytic reactions, there is increasing interest to use this type of chemical transformations in organic synthesis.... 
Ionomer | Michael-type addition | Cellulose | POLYMER SCIENCE | BIOCHEMISTRY & MOLECULAR BIOLOGY | NANOCRYSTALS | ADSORPTION PROPERTY | MAGNETIC CELLULOSE | NANOPARTICLES | SUPPORTED IONIC LIQUIDS | ASYMMETRIC MICHAEL | ALIPHATIC-AMINES | lonomer | NANOCOMPOSITE | CHEMISTRY, APPLIED | HETEROGENEOUS CATALYST | WATER | Index Medicus
Journal Article
Journal of Biomedical Materials Research Part A, ISSN 1549-3296, 08/2011, Volume 98A, Issue 2, pp. 201 - 211
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 09/2016, Volume 81, Issue 17, pp. 7557 - 7565
A convenient, mild and effective conjugate addition of 3-butyn-2-one to a variety of anilines in ethanol is reported. The reaction was monitored and... 
UNSATURATED CARBONYL-COMPOUNDS | MICHAEL-TYPE ADDITIONS | SP-HYBRIDIZED CARBON | ENAMINO-KETONES | METHYL PROPIOLATE | NMR-SPECTROSCOPY | NUCLEAR-MAGNETIC-RESONANCE | CHEMISTRY, ORGANIC | FOURIER-TRANSFORM IR | PRIMARY AMINES | CONFORMATIONAL-ANALYSIS | Usage | Fourier transform infrared spectroscopy | Chemical properties | Aniline
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 03/2016, Volume 57, Issue 10, pp. 1150 - 1153
Journal Article
REACTIVE & FUNCTIONAL POLYMERS, ISSN 1381-5148, 10/2018, Volume 131, pp. 164 - 173
Journal Article
Journal of Molecular Catalysis. B, Enzymatic, ISSN 1381-1177, 02/2014, Volume 100, pp. 121 - 128
Fe O /ZnO core/shell magnetic nanoparticles in 1:1 and 1:2 molar ratios were prepared and characterized by using X-ray powder diffraction, scanning electron... 
Magnetic nanoparticle | Immobilization | Michael-type additions | Lipase | Chalcone | STABILITY | CHEMISTRY, PHYSICAL | ENZYME IMMOBILIZATION | GLASS-BEADS | THERMOMYCES-LANUGINOSUS | OXIDE NANOPARTICLES | CANDIDA-RUGOSA LIPASE | BETA-GALACTOSIDASE | SURFACE | BIOCATALYST | SECONDARY-AMINES
Journal Article
Polymer, ISSN 0032-3861, 2010, Volume 51, Issue 3, pp. 639 - 646
A novel injectable in situ cross-linked hydrogel has been designed via Michael type addition between thiol-modified chitosan (CS–NAC) and PEG diacrylate... 
In situ hydrogel | Michael type addition | Chitosan | POLYMER SCIENCE | ENCAPSULATION | CONTROLLED-RELEASE | DEGRADABLE DEXTRAN HYDROGELS | RHEOLOGICAL CHARACTERIZATION | NASAL ABSORPTION ENHANCEMENT | POLY(ETHYLENE GLYCOL) | GRAFTED CHITOSAN | PART 1 | LINKABLE HYALURONAN HYDROGELS | DRUG-DELIVERY SYSTEMS
Journal Article
TETRAHEDRON LETTERS, ISSN 0040-4039, 01/2014, Volume 55, Issue 1, pp. 267 - 270
Asymmetric conjugate addition of arylboronic acids to 2-nitroacrylamide in the presence of cationic palladium-Chiraphos complex proceeds with high yield and... 
NITRO ACRYLATES | MICHAEL-TYPE HYDROARYLATION | Pd-catalysis | ENANTIOSELECTIVE SYNTHESIS | CHEMISTRY, ORGANIC | ALPHA,BETA-UNSATURATED CARBONYL-COMPOUNDS | Asymmetric Michael addition | Nitroalkenes | ORGANOBORONIC ACIDS | beta-Amino acids | LIGANDS | Arylboronic acids | ELECTRON-DEFICIENT ALKENES | STEREOSELECTIVE-SYNTHESIS
Journal Article
Tetrahedron, ISSN 0040-4020, 07/2012, Volume 68, Issue 27-28, pp. 5619 - 5630
A comprehensive library of - or 1-substituted indoles was formed by conjugate additions of indoline with Michael acceptors followed by an oxidation step. Using... 
Conjugate addition | Indoline | Michael acceptor | Substitution | Catalyst | ALKYLATION | MICHAEL-TYPE ADDITION | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | DIELS-ALDER REACTIVITY | SODIUM SALT | FUNCTIONALIZATION | PRODUCTS | Chemical synthesis | Libraries | Universities and colleges | Conjugates | Synthesis | Heterocyclic aromatic compounds | Tetrahedrons | Tools | Oxidation | Indoles
Journal Article
Research on Chemical Intermediates, ISSN 0922-6168, 07/2017, Volume 43, Issue 7, pp. 3691 - 3709
Journal Article
Journal of Chemical Research, ISSN 1747-5198, 04/2018, Volume 42, Issue 4, pp. 227 - 232
Efficient and flexible syntheses of 1,4-disubstituted quinolizidine-type poison-frog alkaloids using the highly stereoselective Michael-type conjugate addition... 
Michael-type conjugate addition | 1,4-disubstituted quinolizidine | SKIN | NICOTINIC ACETYLCHOLINE-RECEPTORS | CHEMISTRY, MULTIDISCIPLINARY | STEREOCHEMISTRY | Alkaloids
Journal Article
Synlett, ISSN 0936-5214, 09/2010, Volume 2010, Issue 14, pp. 2174 - 2178
Abstract Michael-type addition of enamino esters to 3,4,6-tri-O-benzyl-2-nitro-D-glucal under solvent-free conditions formed C-glycosides in excellent yields... 
letter | C -glycosides | Michael-type addition | solvent-free | CONVENIENT SYNTHESIS | ROUTE | C-glycosides | FERRIER REARRANGEMENT | CHEMISTRY, ORGANIC | GLYCALS | TRANSITION-STATE | KETONES | AMINO-ACIDS | 2-NITROGLYCALS | DERIVATIVES | CONJUGATE ADDITION
Journal Article