methyl acrylate has been researched along with 3-buten-2-one in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (60.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Brummond, KM; Harki, DA; Jackson, PA; Widen, JC | 1 |
| Barber, DS; Das, S; Gavin, T; Geohagen, BC; He, D; Lopachin, RM | 1 |
| Das, S; Gavin, T; Geohagen, BC; LoPachin, RM | 1 |
| Bonnet-Delpon, D; Crousse, B; De, K; Legros, J | 1 |
| Libby, RD; Mehl, RA | 1 |
5 other study(ies) available for methyl acrylate and 3-buten-2-one
| Article | Year |
|---|---|
Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions.
Topics: Cell Line, Tumor; Drug Design; ErbB Receptors; Humans; Ketones; Sulfhydryl Compounds | 2017 |
Structure-toxicity analysis of type-2 alkenes: in vitro neurotoxicity.
Topics: Acrolein; Acrylamide; Acrylates; Aldehydes; Alkenes; Allyl Compounds; Animals; Blotting, Western; Brain; Butanones; Cross-Linking Reagents; Dopamine; Dose-Response Relationship, Drug; Ethylmaleimide; Hydralazine; In Vitro Techniques; Male; Membrane Fusion Proteins; Neurons; Propanols; Rats; Rats, Sprague-Dawley; Structure-Activity Relationship; Sulfhydryl Compounds; Sulfhydryl Reagents; Synaptic Vesicles; Synaptosomes; Tandem Mass Spectrometry | 2007 |
Neurotoxic mechanisms of electrophilic type-2 alkenes: soft soft interactions described by quantum mechanical parameters.
Topics: 1-Propanol; Acrolein; Acrylamide; Acrylates; Alkenes; Animals; Butanones; Corpus Striatum; Cysteine; Dopamine; Ethylmaleimide; Male; Neurotoxicity Syndromes; Propanols; Quantum Theory; Rats; Rats, Sprague-Dawley; Synaptosomes | 2007 |
Solvent-promoted and -controlled aza-Michael reaction with aromatic amines.
Topics: Acrylates; Alkylation; Amines; Aza Compounds; Butanones; Solvents | 2009 |
Characterization of covalent Ene adduct intermediates in "hydride equivalent" transfers in a dihydropyridine model for NADH reduction reactions.
Topics: Acrylates; Butanones; Dihydropyridines; Magnetic Resonance Spectroscopy; Models, Molecular; NAD; Oxidation-Reduction; Silanes | 2012 |