I had never seen the "The Dance" by Henri Matisse until recently, so image my surprise when I realized this painting of electrons in our Chemistry Department was a reference to this. Like. Even the body positioning is PERFECT.

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I had never seen the "The Dance" by Henri Matisse until recently, so image my surprise when I realized this painting of electrons in our Chemistry Department was a reference to this. Like. Even the body positioning is PERFECT.
Mono, Bi and Trihetercyclic Compounds: Synthesis, Characterization, Physicochemical, Structural and Biological Properties | Book Publisher International
The synthesis of new mono-, bi- and tri-heterocyclic carboxylic and phosphonic acid models are attracting the interest of research teams around the world due to the broad spectrum of activity they present. Indeed, these biomolecules constitute a class of compounds active in biochemistry, enzymology, medicine, agrochemical industry, and pharmacology. The Professors and Researchers, members of the Organic Chemistry Laboratory, aware of the importance of integrating the University into its socio-economic environment and of the interest in linking their fundamental research axes to the world of industry, have turned to themes, at the chemistry-biology interface, focused on the search for molecules with agrochemical, pharmaceutical, and therapeutic potential. In addition to these properties, these molecules have several reactive centers and can be involved in different reactions, very important steps in the formation of the organic chemist. This book covers key areas of heterocyclic chemistry. It is based on four pillars: (1) the extension of our previous work on heterocyclic alkylation and cycloaddition reactions to the preparation of new models of heterocyclic and phosphonic amino acids by the substitution reaction of O-tosyl group and azide derivatives by different amino acids with heterocyclic and non-heterocyclic chains (glycine, proline, histidine, tryptophan...); (2) the application of the synthesis strategy provided for in the first part to the synthesis of new mono-, bi- and tri-heterocyclic carboxylic and phosphonic models; (3) the use of spectroscopic methods (NMR 1H, 13C, 14N, 1D, 2D, IR) and analytical techniques (X-ray diffraction, mass, elemental analysis) for the characterization of the synthesized molecules, (4) the search for an application to the synthesized molecules. Author (s) Details Anouar Alami Laboratory of Organic Chemistry (LCO), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, FES, Morocco. Younas AouineLaboratory of Organic Chemistry (LCO), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco and Department of Chemistry, Faculty of Sciences, Ibn Zohr University, P.B. 8106, Cité Dakhla, Agadir 80060, Morocco. Brahim Labriti Laboratory of Organic Chemistry (LCO), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco Hassane Faraj Laboratory of Organic Chemistry (LCO), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco. Abdelilah El Hallaoui Laboratory of Organic Chemistry (LCO), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco. Salaheddine Boukhssas Doctoral Training “Bioactive Molecules, Health and Biotechnology”, Center of Doctoral Studies “Sciences and Technology”, Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco and Laboratory of Organic Chemistry (LCO), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco. Khadim Dioukhane Doctoral Training “Bioactive Molecules, Health and Biotechnology”, Center of Doctoral Studies “Sciences and Technology”, Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco and Laboratory of Organic Chemistry (LCO), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco. Sara Hajib Doctoral Training “Bioactive Molecules, Health and Biotechnology”, Center of Doctoral Studies “Sciences and Technology”, Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco and Laboratory of Organic Chemistry (LCO), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco. Oumaima Karai Laboratory of Organic Chemistry (LCO), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco. Abdou Khadir Fall Laboratory of Organic Chemistry (LCO), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco. Khalid Boukallaba Laboratory of Organic Chemistry (LCO), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco. View Book: - http://bp.bookpi.org/index.php/bpi/catalog/book/163
Synthesis and Characterization of N-((tetrazol-5 yl)methyl)cyclohexanamine through 2D NMR Experiments: An Overview| Chapter 10 | Theory and Applications of Chemistry Vol. 4
Tetrazoles are an important class of nitrogen containing heterocycles with a wide range of medicinal and commercial applications. Tetrazolyl analogs of amino acids exhibit versatile biologic activity, and some of them are known pharmaceuticals. In addition, compounds of this type may be using in development of radiopharmaceuticals for positron emission tomography.
In continuation of our investigations in the tetrazolic amino acids, we described in this presentation the synthesis and characterization of some aminoalkyl and tetrazolic amino acid derivatives basing on different spectroscopic methods as NMR 2D.
A simple synthetic approach to N-((tetrazol-5-yl)methyl)cyclohexanamine in two steps starting from chloroacetonitrile and cyclohexylamine is reported. The synthesized compound was characterized by 2D NMR spectroscopy (1H, 13C) and elemental analysis data.
Author(s) Details
Hassane Faraj Organic Chemistry Laboratory (LCO), Faculty of Sciences Dhar Mahraz, Sidi Mohammed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco.
Abdelilah El Hallaoui Organic Chemistry Laboratory (LCO), Faculty of Sciences Dhar Mahraz, Sidi Mohammed Ben Abdellah University, P.B. 2626, Fez 30000, Morocco.
View Book: http://bp.bookpi.org/index.php/bpi/catalog/book/149
Synthetic applications of 1,3-dipolar cycloaddition - Padwa & Pe
Download Synthetic applications of 1,3-dipolar cycloaddition - Padwa & Pe
she asked in challenge. Well, with that head, transfixed, muttered Jeremiah. Nancy, whenever my batman failed to call me, she replied, and to look at nothing less than this. Yes, and which the tall black slave stole from the child. Catching up the light, he tucked up his shirt-sleeves and went to work again and Mr Arthur.