Results 101 to 110 of about 41,169 (164)
Retraction Note: New Acetamidine Cu(II) Schiff base complex supported on magnetic nanoparticles pectin for the synthesis of triazoles using click chemistry. [PDF]
Siuki HK, Kargar PG, Bagherzade G.
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Structural elucidation, biological significance and computational approach of Copper(ii), Nickel(ii) and Cobalt(ii) with bidentate schiff base of N-(Napthalene-1-ylmethylene)isonicotinohydrazide. [PDF]
Islam MA +11 more
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Journal of the Chemical Society, Chemical Communications, 1976
Although very few examples of chemiluminescent Schiff bases have been described, and attempts to extend this class of reaction have hitherto been unsuccessful, it is now shown that these compounds are generally chemiluminescent on oxidation, with reasonable efficiency.
Frank McCapra, Alexander Burford
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Although very few examples of chemiluminescent Schiff bases have been described, and attempts to extend this class of reaction have hitherto been unsuccessful, it is now shown that these compounds are generally chemiluminescent on oxidation, with reasonable efficiency.
Frank McCapra, Alexander Burford
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Sulfenylation of chiral Schiff bases
Amino Acids, 1994The purpose of this study was to examine the conditions of sulfenylation reactions of chiralα-amino esters Schiff bases to protect the chirality in theα-position.
A, Bentama +4 more
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Direct diacylation of schiff bases
Tetrahedron Letters, 1988Abstract A novel diacylation of Schiff bases occurs using catalytic quantities of cobalt carbonyl and phase transfer catalysis conditions.
VASAPOLLO, Giuseppe, Alper Howard
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Uranyl stabilized Schiff base complex
Chemical Communications, 2007Uranyl Schiff base complex [(UO(2))(2)(Salpro)(OH)(Solvent)(2)] (1) in the presence of excess of ethylenediamine (EDA) does not undergo nucleophilic addition (hydrolysis) and substitution (transamination) reactions due to an extended chelation [2N, 3O + OH] by the flexible backbone.
Mohan S, Bharara +2 more
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Journal of Macromolecular Science: Part A - Chemistry, 1967
Abstract This paper compares the syntheses and the thermal stabilities of twelve related conjugated, pseudoconjugated, and nonconjugated Schiff base polymers of the general formula in which Z represents The polymers were prepared (a) by the condensation of Z(NH2)2 and p-C6 H4(CHO)2 in (1) solution and (2) as melts, and (b) by three new Schiff base ...
G. F. D'alelio +3 more
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Abstract This paper compares the syntheses and the thermal stabilities of twelve related conjugated, pseudoconjugated, and nonconjugated Schiff base polymers of the general formula in which Z represents The polymers were prepared (a) by the condensation of Z(NH2)2 and p-C6 H4(CHO)2 in (1) solution and (2) as melts, and (b) by three new Schiff base ...
G. F. D'alelio +3 more
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Polymeric Schiff Bases. III. Some Prototype Exchange Reactions of Schiff Bases
Journal of Macromolecular Science: Part A - Chemistry, 1967Abstract The amine moiety in Schiff bases can be exchanged quantitatively by another amine to yield new Schiff bases if the volatility of the replacing amine is lower than the derived amine, thereby allowing the latter to distilled from the reaction mass. This amine exchange was shown to be quantitative also for diamines and di-Schiff bases. Similarly,
G. F. D'alelio +3 more
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Pyridoxal-derived Schiff’s bases
Russian Journal of General Chemistry, 2015Over the past few decades synthesis of functionalized derivatives of pyridoxal (vitamin B6) and study of their biological activity have received a great deal of interest [1–3]. Among these compounds, monoand bis-azomethines of pyridoxal occupy an important place [4–6].
L. K. Kibardina +4 more
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