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This chemistry blog is aimed mainly at senior high school students or first year university students. 15
Relaxing Conformational Constraints in Dynamic Macrocycle Synthesis. A HPLC method for the quantification of butyramide and acetamide at ppb levels in hydrogeothermal waters. Find more information about Crossref citation counts. It is the simplest amide derived from acetic acid. Theoretical elucidation of rare earth extraction and separation by diglycolamides from crystal structures and DFT simulations. Dae Eon Jung, Youngho Eom, Byoung Chul Kim. Acta Crystallographica Section C Structural Chemistry. Complete basis set calculations (CBS-QB3) were used to compute the CN rotation barriers for acetamide and eight related compounds, including acetamide enolate and O-protonated acetamide. Huixia Liu, Xiaojun Deng, Xie Huang, Nan Ji, Wei He. Jae-Seung Lee, Ravinder R. Regatte, Alexej Jerschow. ja0663024si20070104_092731.pdf (988.46 kb), http://pubs.acs.org/page/copyright/permissions.html, https://doi.org/10.1021/acs.orglett.0c01488, https://doi.org/10.1021/acs.orglett.9b04413, https://doi.org/10.1021/acs.orglett.9b03274, https://doi.org/10.1021/acs.orglett.9b02961, https://doi.org/10.1021/acs.orglett.9b02513, https://doi.org/10.1021/acs.orglett.8b03175, https://doi.org/10.1021/acs.orglett.8b02323, https://doi.org/10.1021/acs.chemrev.7b00514, https://doi.org/10.1021/acs.orglett.8b00086, https://doi.org/10.1021/acsmacrolett.7b00896, https://doi.org/10.1021/acs.orglett.7b02877, https://doi.org/10.1021/acssuschemeng.7b01092, https://doi.org/10.1021/acs.orglett.7b00913, https://doi.org/10.1021/acs.orglett.7b00989, https://doi.org/10.1021/acs.macromol.7b00579, https://doi.org/10.1038/s41467-020-17588-5, https://doi.org/10.1016/j.comptc.2020.113001, https://doi.org/10.1016/j.trechm.2020.08.001, https://doi.org/10.1016/j.tetlet.2020.152444, https://doi.org/10.1016/j.molstruc.2020.129423, https://doi.org/10.1016/j.jre.2020.09.013, https://doi.org/10.1016/j.polymer.2020.122750, https://doi.org/10.1016/j.molstruc.2019.127645, https://doi.org/10.1016/j.procbio.2019.11.021, https://doi.org/10.1016/j.foodhyd.2019.105316, https://doi.org/10.1016/j.molstruc.2019.07.077, https://doi.org/10.1016/j.snb.2019.127047, https://doi.org/10.1007/s10337-019-03763-4, https://doi.org/10.1134/S0036024419100091, https://doi.org/10.1080/00397911.2019.1616761, https://doi.org/10.1007/s13233-019-7058-8, https://doi.org/10.1107/S2053229618013463, https://doi.org/10.3390/molecules23112859, https://doi.org/10.3390/molecules23102615, https://doi.org/10.3390/molecules23102681, https://doi.org/10.1016/j.jorganchem.2018.07.014, https://doi.org/10.1016/j.tetlet.2018.01.097, https://doi.org/10.1016/j.comptc.2017.05.004, https://doi.org/10.1016/j.electacta.2017.02.013, https://doi.org/10.1016/j.eurpolymj.2017.01.038, https://doi.org/10.1016/B978-0-12-409547-2.12517-X, https://doi.org/10.1016/j.cej.2015.07.070, https://doi.org/10.1016/j.conbuildmat.2015.10.085, https://doi.org/10.1016/j.conbuildmat.2015.10.087, https://doi.org/10.1016/j.molstruc.2015.08.014, https://doi.org/10.1016/j.colsurfa.2015.05.057, https://doi.org/10.1016/j.tet.2015.07.039, https://doi.org/10.1016/j.cplett.2015.03.028, https://doi.org/10.1007/s11434-013-5859-2, https://doi.org/10.1016/j.jpba.2013.03.019, https://doi.org/10.1007/s00396-012-2706-y, https://doi.org/10.1016/j.jchromb.2012.03.031, https://doi.org/10.1007/s00214-012-1178-y, https://doi.org/10.1016/j.jcis.2011.05.033, https://doi.org/10.1016/j.molstruc.2009.04.011, https://doi.org/10.1016/j.polymer.2008.06.036, https://doi.org/10.1016/j.chemphys.2007.12.002, https://doi.org/10.1016/j.theochem.2008.01.018, https://doi.org/10.1016/j.theochem.2007.11.001, https://doi.org/10.1016/j.theochem.2007.10.014. Ervin Kovács, Balázs Rózsa, Attila Csomos, Imre Csizmadia, Zoltán Mucsi. Vladimir Y. Mikshiev, Alexander F. Pozharskii, Alexander Filarowski, Alexander S. Novikov, Alexander S. Antonov, Peter M. Tolstoy, Mikhail A. Vovk, Olesya V. Khoroshilova. ®
Shicheng Shi, Guangrong Meng, Michal Szostak. Pyrene-Modified Unlocked Nucleic Acids: Synthesis, Thermodynamic Studies, and Fluorescent Properties. 4 + 4 + 6 + 5 + 1*2) = 24, Therefore, P = 6n Block-Localized Wavefunction (BLW) Method at the Density Functional Theory (DFT) Level. Theoretical Chemistry - Lewis Electron Dot Structures, Analytical Chemistry - Acid & Base Equilibria, Analytical Chemistry - Gas Chromatography / Mass Spectrometry, Analytical Chemistry - Liquid Chromatography, Analytical Chemistry - Statistical Analysis of Experimental Data, Chemical News & Interesting - Periodic Table - Elements, Organic Chemistry - Nucleophilic Substitution Reactions, Physical & Theoretical Chemistry - Chemical Kinetics, Physical & Theoretical Chemistry - Computational Chemistry, Physical & Theoretical Chemistry - Electrochemistry, Physical & Theoretical Chemistry - Lewis Structures, Physical & Theoretical Chemistry - Properties of Solutions, Physical & Theoretical Chemistry - Thermochemistry, Theoretical Chemistry - Lewis Electron Dot Structures and Reactivity, As a general solvent (molten acetamide is excellent solvent for many organic and inorganic compounds). Amide Bond Activation: The Power of Resonance. Sibel Demir, Sukriye Cakmak, Necmi Dege, Halil Kutuk, Mustafa Odabasoglu, R. Aysun Kepekci. Synergistic Activation of Amides and Hydrocarbons for Direct C(sp
Copper-catalyzed radical cascade oxyalkylation of olefinic amides with simple alkanes: highly efficient access to benzoxazines. Methanol production from CO
Structure, properties, spectra, suppliers and links for: Acetamide, 60-35-5, 544-44-5, 53318-35-7. New Generation Hole Transporting Materials for Perovskite Solar Cells: Amide-Based Small-Molecules with Nonconjugated Backbones. Electrophilicity Scale of Activated Amides:
An efficient computational model to predict protonation at the amide nitrogen and reactivity along the C–N rotational pathway. Dean Sherry. Tongqing Xie, Li Yang, Xingxing Sun, Jun Jiang, Xuepeng Zhang, Yi Luo, Guoqing Zhang. Structures, Internal Rotor Potentials, and Thermochemical Properties for a Series of Nitrocarbonyls, Nitroolefins, Corresponding Nitrites, and Their Carbon Centered Radicals. A Comprehensive Theoretical Study of Amide Resonance, Intramolecular Hydrogen Bonding, and π-Electron Delocalization in Diformyl and Dithioformyl Amine. Zhiguo Zhang, Lianqiang Zhang, Xinyu Duan, Xiangqian Yan, Yan Yan, Qingfeng Liu, Tongxin Liu, Guisheng Zhang. N NMR chemical shifts of sterically-hindered amides: ground-state destabilization in amide electrophilicity. Yann Bourne-Branchu, Corinne Gosmini, Grégory Danoun. Journal of Chemical Theory and Computation. Ling Li, Lu Hua Li, Sugeetha Ramakrishnan, Xiujuan J. Dai, Kevin Nicholas, Ying Chen, Zhiqiang Chen, and Xiaowei Liu . Hydrogen bonded dimers of small alkyl substituted amides: Structures, energetics, and spectral analyses based on density functional theory calculations. Christophe Morell, Alexandre Hocquet, André Grand, Brigitte Jamart-Grégoire. Chemistry of Bridged Lactams and Related Heterocycles. Mechanisms behind the enhancement of thermal properties of graphene nanofluids. Conformational Distributions of N-Acetyl-L-cysteine in Aqueous Solutions: A Combined Implicit and Explicit Solvation Treatment of VA and VCD Spectra. Synthesis of Biaryls through Nickel-Catalyzed Suzuki-Miyaura Coupling of Amides by Carbon-Nitrogen Bond Cleavage. Conquering amide planarity: Structural distortion and its hidden reactivity. Griselda Hernández, Janet S. Anderson and David M. LeMaster . Structural Characterization of N-Alkylated Twisted Amides: Consequences for Amide Bond Resonance and N−C Cleavage. Eric D. Glendening, Clark R. Landis, Frank Weinhold. International Journal of Chemical Kinetics. N-Methyldehydroamino acids promote a configuration cis of N-methylamide bond. the Altmetric Attention Score and how the score is calculated. O NMR and
Acetamide (systematic name: ethanamide) is an organic compound with the formula CH3CONH2. N
Highly Chemoselective Synthesis of Indolizidine Lactams by SmI
Structures and energetic properties of 4-halobenzamides. iso
Vertically aligned multi-walled carbon nanotubes based flexible immunosensor for extreme low level detection of multidrug resistant leukemia cells. Palladium(II)-Catalyzed Oxidative Cascade Cyclization Reactions of Anilides and Anilines: Scope and Mechanistic Investigations. Acetamide can be considered an intermediate between acetone, which has two methyl (CH3) groups either side of the carbonyl (CO), and urea which has two amide (NH2) groups in those locations. However, chemistry topics of general interest are going to be included. Colloids and Surfaces A: Physicochemical and Engineering Aspects. Alternatives to Gadolinium-Based Metal Chelates for Magnetic Resonance Imaging. Lukas Fischer, Alexander K. Strzelczyk, Nils Wedler, Christian Kropf, Stephan Schmidt, Laura Hartmann. an integrated, formamide-assisted approach. Fourier Transform Infrared Spectroscopy characterization of aging-related properties of original and nano-modified asphalt binders. Resonance-assisted amide protonation in dutasteride hydrochloride salt. 15
Nehal Fayek Farid, Nada Sayed Abdelwahab. -methyl-α,β-dehydroamino acids. Jorge G. Uranga, Aswin Gopakumar, Tim Pfister, Gunay Imanzade, Loris Lombardo, Gabriela Gastelu, Andreas Züttel, Paul J. Dyson. 3
Xiujing Peng, Jianhui Su, Hao Li, Yu Cui, Jin Yong Lee, Guoxin Sun. The first resonance structure of acetamide, CH, CONH,, is shown. Zhi-Yong Zeng, Yi-Siang Wang, Sheng D. Chao. Experimental and theoretical spectroscopic characterization, NLO response, and reactivity of the pharmacological agent spilanthol and analogues. Bekir Salgin, Önnaz Özkanat, Johannes M. C. Mol, Herman Terryn, and Michael Rohwerder . Hind Hadi, Ahmad Makahleh, Bahruddin Saad. Feng Hu, Roger Lalancette, Michal Szostak. Dan Li, Jingjing Meng, Yuan Niu, Hongmin Zhao, Chunjun Liang. Effect of structural isomerism and polymer end group on the pH-stability of hydrogen-bonded multilayers. Wenchao Lu, Fangwei Liu, Rifat Emre, and Jianbo Liu .