2109-66-2Relevant articles and documents
Tetranuclear Zn complex covalently immobilized on sulfopropylsilylated mesoporous silica: An efficient catalyst for ring opening reaction of epoxide with amine
Bandyopadhyay, Mahuya,Bandyopadhyay, Rajib,Das, Sourav,Jadav, Divya,Kubota, Yoshihiro,Shukla, Pooja
, (2020)
Tetranuclear Zn complex, [Zn4(L)2(LH)2((CH3)2SO)2]·2CH3OH·(CH3)2SO·H2O (1) [where LH3 = 3-(E)-(2-hydroxyphenylimino)methyl-4-hydroxy-5-hydroxymethylphenyl (LH3)] was prepared and characterized by single-crystal X-ray analysis. Then, it was incorporated to the sulfopropylsilylated MCM-48, MCM-41 and SBA-15 mesoporous silica materials. The prepared materials were thoroughly characterized by XRD, FT-IR, N2 adsorption/desorption analysis, NH3-TPD, TGA, SEM-EDX and ICP-OES measurements. These catalysts were successfully used for the ring opening reaction of propylene oxide with morpholine producing the corresponding β-aminoalcohols. An abrupt increase in catalytic activities was observed after anchoring of the tetranuclear Zn complex onto the inner surface of sulfopropylsilylated mesoporous materials. Among all the catalysts, the tetranuclear Zn complex incorporated MCM-48 was found to be most active in this reaction system and gave maximum 95% conversion. Catalysis by the tetranuclear Zn complex immobilized on MCM-48 was totally heterogeneous and the catalyst was recyclable up to 4 times without leaching.
Micellization and antimicrobial properties of N-alkyl-(2-hydroxypropyl)morpholinium bromides
Ahmadova, Gulnara A.,Huseynova, Khuraman A.,Mammadov, Rustam Kh.,Muradova, Sevda A.,Qasimova, Fatma I.,Rahimov, Ravan A.,Rustamova, Inara V.,Zubkov, Fedor I.
, (2021)
New ionic-liquid cationic surfactants have been synthesized on the basis of alkyl (C9, C10, C12, C14) bromides and 1-(4-morpholinyl)-2-propanol. Surface activity and specific electroconductivity of aqueous solutions of the obtained surfactants have been studied by tensiometric and conductometric methods. Depending on the length of the alkyl chain, the values of critical micellization concentration (CMC), maximum adsorption (Гmax), area of minimal cross-sectional surface of polar group of the surfactant (Amin), adsorption efficiency (pC20), surface pressure (πCMC), binding degree of the counter-ion (β), changes of Gibbs free energies of micellization and adsorption processes (ΔGmic and ΔGad) have been determined. Antimicrobial properties of the synthesized ionic-liquid surfactants have been studied on the example of different bacteria and fungus.
COMPOUNDS FOR THE MODULATION OF MYC ACTIVITY
-
Paragraph 283; 284, (2017/05/31)
The present invention provides novel compounds of Formulas (I) and (II) and pharmaceutically acceptable salts, solvates, hydrates, tautomers, stereoisomers, isotopically labeled derivatives, and compositions thereof. Also provided are methods and kits involving the compounds or compositions for treating or preventing proliferative diseases, e.g., cancers (e.g., breast cancer, prostate cancer, lymphoma, lung cancer, pancreatic cancer, ovarian cancer, neuroblastoma, or colorectal cancer), benign neoplasms, angio genesis, inflammatory diseases, fibrosis (e.g., polycystic kidney disease), autoinflammatory diseases, and autoimmune diseases in a subject.
A solvent free method for preparation of β-amino alcohols by ring opening of epoxides with amines using MCM-22 as a catalyst
Baskaran, Thangaraj,Joshi, Akanksha,Kamalakar, Gunda,Sakthivel, Ayyamperumal
, p. 50 - 55 (2016/07/06)
β-amino alcohols were synthesized at room temperature employing microporous MCM-22 zeolite as catalyst in an eco-friendly manner without using solvent. The zeolite MCM-22 showed promising activity for the conversion of primary and secondary amines into β-amino alcohols under mild reaction conditions. The catalytic activity remains intact for three recycles.
Tetragonal versus hexagonal: Structure-dependent catalytic activity of Co/Zn bimetallic metal-organic frameworks
Pariyar, Anand,Asl, Hooman Yaghoobnejad,Choudhury, Amitava
supporting information, p. 9250 - 9257 (2016/09/28)
Tetragonal and hexagonal phases of monometallic Zn and bimetallic Co/Zn metal-organic frameworks (MOFs), with secondary building units (SBUs) containing a M3O (M = metal) cluster, were synthesized from identical constituents using a benzenetricarboxylate (BTC3-) linker that forms decorated 3,6- and 3,5-connected networks, respectively. There exist subtle differences between the SBUs; one of the metal atoms in the M3O cluster in the tetragonal phase has one dissociable DMF solvent molecule while that in the hexagonal phase has three. Connectivities between the SBUs form one-dimensional channels in both MOFs. These MOFs catalyze the chemoselective addition of amines to epoxides, giving exclusively β-hydroxyamine under heterogeneous conditions. A ring-opening reaction of a symmetrical epoxide showed that the hexagonal phase diastereoselectively yields trans-alcohol, exhibiting an exquisite model for structure-dependent activity.
Platinum-Catalyzed, Terminal-Selective C(sp3)-H Oxidation of Aliphatic Amines
Lee, Melissa,Sanford, Melanie S.
supporting information, p. 12796 - 12799 (2015/10/28)
This Communication describes the terminal-selective, Pt-catalyzed C(sp3)-H oxidation of aliphatic amines without the requirement for directing groups. CuCl2 is employed as a stoichiometric oxidant, and the reactions proceed in high yield at Pt loadings as low as 1 mol%. These transformations are conducted in the presence of sulfuric acid, which reacts with the amine substrates in situ to form ammonium salts. We propose that protonation of the amine serves at least three important roles: (i) it renders the substrates soluble in the aqueous reaction medium; (ii) it limits binding of the amine nitrogen to Pt or Cu; and (iii) it electronically deactivates the C-H bonds proximal to the nitrogen center. We demonstrate that this strategy is effective for the terminal-selective C(sp3)-H oxidation of a variety of primary, secondary, and tertiary amines.
Synthesis of piperazino and morpholino derivatives of aryloxypropane with potential analgesic and possible antimigraine activities
Ismaiel, Abdulkhader M.,Gad, Laila M.,Ghareib, Salah A.,Bamanie, Faida H.,Moustafa, Mohamed A.
experimental part, p. 381 - 387 (2012/06/05)
Modeling studies demonstrate that aryl piperazines (I), aryloxyalkylamines (II), phenylalkykamines (III) and indolylalkylamines (VI) may interact at 5-HT receptors in a similar manner. Examination of these structures (I-VI) reveals that all possess an aromatic moiety and terminal amine binding sites (Glennon et al., J Med Chem 32(8):1921-1926, 1989). In the present investigation a new series of aryloxyalkylamines (4, 5, 8, and 9) was designed and synthesized, in which the aromatic moiety is a phenyl group substituted at the 2,3-, 2,4-, 2,5-, or 2,6-positions by halogens and the terminal amine is N-methylpiperazine, or morpholine. In addition, the alkyl side chain is ethyl, or substituted ethyl at the α- or β-carbon by a methyl group. The length of the alkyl chain that separates the terminal amine from the ether oxygen atom of the aryloxy group is of major importance, and two-carbon chain appears optimal. The structures of the new compounds were assessed by microanalyses, IR, and NMR. The analgesic activity of selected compounds was performed on experimental animals and proved to be in the range of 85-100% relative to aspirin. Springer Science+Business Media, LLC 2011.
Regioselective ring opening in epoxides under the action of amines in water medium
Talybov,Abbasov,Mamedbeili,Kochetkov
experimental part, p. 1819 - 1824 (2011/02/24)
Amino(bis-amino)derivatives of 2-propanol were synthesized by ring opening in epoxides under the action of amines in water medium using environmentally safe methods. The structure of the compounds obtained was established by elemental analysis and the IR, 1H and 13C NMR spectroscopy. It was found that these substances are effective bactericides. They suppress the growth of the sulfate-reducing bacteria and exhibit high anticorrosive properties.
Hydrophobic amplification of noncovalent organocatalysis
Kleiner, Christian M.,Schreiner, Peter R.
, p. 4315 - 4317 (2007/10/03)
The effects of hydrogen-bonding organocatalysts and water for the acceleration of epoxide openings with a variety of nucleophiles are additive and lead to excellent yields of the catalyzed reactions in water. The Royal Society of Chemistry 2006.
Highly chemoselective addition of amines to epoxides in water
Azizi, Najmodin,Saidi, Mohammad R.
, p. 3649 - 3651 (2007/10/03)
(Chemical Equation Presented) Aminolysis of a variety of epoxides by aliphatic and aromatic amines in water, in the absence of any catalyst with high yields, is reported. β-Amino alcohols were formed under mild conditions with high selectivity and in excellent yields.
