and you may need to create a new Wiley Online Library account. ; Colombatto, S. Advanced glycation end-products (AGEs): Involvement in aging and in neurodegenerative diseases. ; Tang, T.P.
Gupta, K.C. Claisen, L. Ueber eine eigenthümliche Umlagerung. Quinoxaline-based Schiff base transition metal complexes: Review.
; Lough, A.J.
Learn more. Hirabayashi, T.; Itoh, K.; Sakai, S.; Ishii, Y. Insertion reactions of diethylaluminium derivatives II.
; Weingarten, H. A versatile new enamine synthesis.
Sinha, D.; Tiwari, A.K.
Saravanan, G.; Pannerselvam, P.; Prakash, C.R.
E ; Aboaly, M.M. Cainelli, G.; Giacomini, D.; Mezzina, E.; Panunzio, M.; Zarantonello, P. Cainelli, G.; Panunzio, M.; Contento, M.; Giacomini, D.; Mezzina, E.; Giovagnoli, D. Preparation of 1,2 aminols from cyanohydrins via. Schiff, U. Giornale di scienze naturali ed economiche. ; Rutjes, F.P.J.T. reaction of diethylaluminium dimethylamide and diethylaluminium ethanethiolate with nitriles.
Addition der Cα-H-bindung von. ; Lai, M.M.C.
D’hooghe, M.; van Brabandt, W.; Dekeukeleire, S.; Dejaegher, Y.; de Kimpe, N. Highly stereoselective synthesis of beta-lactams utilizing alpha-chloroimines as new and powerful chiral inductors. Enolizable aldehydes were supposed to behave in the same way [, In analogy of classical preparation of Schiff Bases silyl-imines, This method allows the preparation of tin imines from enolizable and non enolizable aldehydes and ketones, in good yield and under very mild conditions (, As a versatile precursor for organic syntheses, we can identify, in an oversimplification, four different types of reactions in which Schiff bases have been found extremely important applications: (a) addition of organometallic reagents or hydride to C=N bond to afford compounds of structure, The same criteria have been used for all the applications reported in, The importance of Schiff bases as intermediates in bio-processes is very well established: suffice it to mention one of the very basic process of life: the transamination reaction (, Other important bio-processes, that lately are attracting the interest of chemists and biologists, are related to the glycation of albumin that leads to the formation of important biomarkers, which are predictive of type II diabetes [, There are numerous publications covering the use of Schiff bases in therapeutic or biological applications either as potential drug candidates or diagnostic probes and analytical tools.
III. Meller, A.; Maringgele, W. Monomere und dimere hochhalogenierte Iminoborane. Microwave-assisted preparation of a series of Schiff base without solvent has also been reported. Eco-friendly synthesis of imines by ultrasound irradiation. ; Gavrilyuk, J.I.
Soule, J.-F.; Miyamura, H.; Kobayashi, S. Selective imine formation from alcohols and amines catalyzed by polymer incarcerated gold/palladium alloy nanoparticles with molecular oxygen as an oxidant. Since first synthesis of imine, number of methods has been discovered to enhance reaction yield, decrease reaction time as well as reduce hazardous reagents and reaction conditions.
J. Chem. ) and V( Keywords: Schiff base, synthetic methodology, biological applications. ; Batey, R.A. Lewis acid catalyzed three-component Hetero-Diels-Alder (Povarov) reaction of. ; Desai, K.R. Diethylaminophenyl-based Schiff base Cu(
Catalytic asymmetric Hetero-Diels-Alder reactions of carbonyl compounds and imines. Frischmann, P.D. Privileged chiral catalysts.
Synthesis of novel Schiff bases containing arylpyrimidines as promising antibacterial agents. Metal Complexes of a Novel Schiff Base Based on Penicillin: Characterization, Molecular Modeling, and Antibacterial Activity Study. (Über die katalytische Wirkungsweise von Halogenwasserstoffsäuren bei Kondensationen, II).
Sriram, D.; Yogeeswari, P.; Myneedu, N.S; Saraswat, V. Abacavir prodrugs: Microwave-assisted synthesis and their evaluation of anti-HIV activities.
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