Dynamic NMR and Theoretical Study of Hindered Internal Rotation about the C-N Bond in 4-(Phenyl) Acetyl Morpholine☆
-
Add time:08/16/2019 Source:sciencedirect.com
Variable-temperature 13C NMR spectroscopy is used to investigate barrier of C-N internal rotation in compound 4- (Phenyl) acetyl morpholine, and then with simulation of band shape broadening pattern at coalescence region, rate constants of exchange were obtained for all temperatures. For simulation of line-shape broadening Spin works software (version 3.1) was used, that with two interfaces made possible simulation with two band shape simulator programs, Dynamic Nuclear Magnetic Resonance (DNMR) and MEXICO. For obtaining the thermodynamic activation parameters
We also recommend Trading Suppliers and Manufacturers of N-(4-Acetyl-phenyl)-N-benzyl-methanesulfonamide (cas 110698-70-9). Pls Click Website Link as below: cas 110698-70-9 suppliers
Prev:Structure-based design and synthesis of 1H-pyrazolo[3,4-d]pyrimidin-4-amino derivatives as Janus kinase 3 inhibitors
Next:Original articleSynthesis and QSAR modeling of 2-acetyl-2-ethoxycarbonyl-1-[4(4′-arylazo)-phenyl]-N,N-dimethylaminophenyl aziridines as potential antibacterial agents) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Calculation of 13C Nuclear Magnetic Shielding Constants Using Optimally Selected Basis Functions in 4-(phenyl) Acetyl Morpholine☆08/19/2019
- A new chemoenzymatic approach to the synthesis of chiral 4-aryl-1,4-dihydro-2H-isoquinolines via the enzymatic resolution of 2-acetyl-4-phenyl-1,4-dihydro-2H-isoquinolin-3-one08/18/2019
- Original articleSynthesis and QSAR modeling of 2-acetyl-2-ethoxycarbonyl-1-[4(4′-arylazo)-phenyl]-N,N-dimethylaminophenyl aziridines as potential antibacterial agents08/17/2019
