261630-87-9Relevant academic research and scientific papers
Solvent extraction of Ag(I) and Cu(II) with new macrocyclic Schiff bases
Kedy, Souad,Kandil, Farouk,Almhna, Nadeem
, p. 525 - 528 (2012)
Two new macrocyclic Schiff bases (II) and (III) containing nitrogen - oxygen donor atoms were synthesized by reaction between diethylene triamine or 2,2'-(ethylenedioxy)bis(ethylamine) and the intermediate compound: 1,4-bis(6-methoxy-2-formylphenyl)-1,4-d
Urease inhibition studies of six Ni(II), Co(II) and Cu(II) complexes with two sexidentate N2O4-donor bis-Schiff base ligands: An experimental and DFT computational study
Fan, Yuhua,Jin, Fan,Wang, Hu,Xu, Cungang,Zhang, Dongmei,Zhang, Xia
, (2020)
Six novel complexes, [Ni(C36H34N2O10)]·2.25CH3OH·0.5C4H10O (1), [Co(C36H34N2O10)] (2), [Cu(C36H34N2O
Ring-closing metathesis reaction-based synthesis of new classes of polyether macrocyclic systems
Naveen,Babu, Srinivasarao Arulananda
supporting information, p. 7758 - 7781 (2015/09/08)
Ring closing metathesis (RCM) reactions of suitable substrates having terminal olefins, which are assembled from various linkers and hydroxy benzaldehydes and syntheses of a wide range of 16-30 membered, new crown ether-type polyether, aza-polyether, bis aza-polyether macrocycles and dilactone moiety embedded polyether macrocycles (macrolides) are reported. After the ring-closure reaction, installation of different functional groups and functional group modification on the periphery of the synthesized polyether/crown ether macrocycles obtained in the RCM reactions are accomplished using the epoxidation, oxidation and catalytic hydrogenation-based synthetic transformations. Along this line, the syntheses of a variety of polyether macrocycles possessing epoxide or α-hydroxy ketone or 1,2-diol functionalities at the periphery have been shown. Furthermore, the synthesized α-hydroxy ketone functionality installed polyether macrocycles were subjected to the allylation and Reformatsky type reactions to obtain homoallyl alcohol moiety-based and lactone ring-appended polyether macrocycles.
