Results 1 to 10 of about 14,359 (248)

Transfer of structural units through imine exchanges, in solution or without solvent: successive transiminations, stimuli (pH)-modulated covalent switches, and mathematical models [PDF]

Frontiers in Chemistry
Transfer of structural units through covalent constitutional (non mechanical) switches based on (bis-)imine/amine exchanges (transiminations), can reversibly be modulated by external stimuli, namely by pH changes through alternate additions of acid and ...
Juan Ramirez, Juan Ramirez, Juan Ramirez, Juan Ramirez, Adrian-Mihail Stadler, Adrian-Mihail Stadler, Adrian-Mihail Stadler   +6 more
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Synthesis and Antimicrobial Evaluation of Some New Oxadiazoles Derived from Phenylpropionohydrazides

Molecules, 2009
In this study a series ofnew1-(2-aryl-5-phenethyl-1,3,4-oxadiazol-3(2H)-yl)ethanones 2a-e was synthesized by the cyclization of imines 1a-e using acetic anhydride. The products were evaluated for anti-bacterial and anti-fungal activity.
Mohammad Ali, Mohammad Shaharyar, Neeraj Kumar Fuloria, Vijender Singh   +3 more
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Cycloruthenated Imines: A Step into the Nanomolar Region

Molecules
A new series of promising and easily accessible antiproliferative agents based on cycloruthenated imines of benzene and thiophene carbaldehydes has been developed and fully characterized using UV-Vis spectroscopy, X-ray diffraction, NMR, HRMS, and cyclic
Arsenii A. Vasil’ev, Ivan I. Troshin, Pavel G. Shangin, Ksenia M. Voroshilkina, Ilya A. Shutkov, Alexey A. Nazarov, Aleksei V. Medved’ko   +6 more
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Design, synthesis, molecular docking study, and biological evaluation of salicylaldimine derivatives as potential histone deacetylases inhibitors (HDACi) and anticancer agents

Archives of Pharmaceutical Sciences Ain Shams University, 2018
Despite the increased success rates of histone deacetylases inhibitors (HDACi) as potent anticancer agents, many metabolic obstacles face the hydroxamic acid-based HDAC inhibitors, which inspired us to develop non-hydroxamate HDAC inhibitors.
Heba M. Hesham, Deena S. Lasheen, Khaled A. M. Abouzid   +2 more
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Asymmetric organocatalytic synthesis of chiral homoallylic amines

Beilstein Journal of Organic Chemistry
In recent decades, the chiral allylation of imines emerged as a key methodology in the synthesis of alkaloids and natural products with 4-, 5- and 6-membered cyclic amine motifs.
Nikolay S. Kondratyev, Andrei V. Malkov
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Enantioselective Hydrogenations with Chiral Titanocenes

Molecules, 2005
In this review article chiral titanocenes and their application for the enantioselective hydrogenations of different unsaturated compounds are discussed, with a special emphasis on the kinetics and the practicality of the developed systems. The nature of
J. Khinast, A. Panarello, O. Vassylyev
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Bis(benzylamine) monomers: One-pot preparation and application in dendrimer scaffolds for removing pyrene from aqueous environments

Beilstein Journal of Organic Chemistry, 2013
Bisimine and bisamine AB2 monomers have been synthesized from 3,5-diaminobenzoic acid and benzaldehyde derivatives without the need for protective groups or purification.
Olivia N. Monaco, Sarah C. Tomas, Meghan K. Kirrane, Amy M. Balija   +3 more
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Solvent-free, Environmentally Benign Syntheses of Some Imines and Antioxidant Activity

Orbital: The Electronic Journal of Chemistry, 2015
Environmentally benign, economically feasible, and solvent-free syntheses of series of imines by the condensation of a substituted hydroxynaphthyl ketone with several substituted iodoanilines under grinding approach are described.
Sainath B. Zangade, Avinash Shinde, Shivaji Chavan, Yeshwant Vibhute   +3 more
doaj  

amine imines

, 2014
Citation: 'amine imines' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.A00272 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
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nitrile imines

, 2014
Citation: 'nitrile imines' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.N04149 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +1 more source