162586-72-3Relevant academic research and scientific papers
Efficient tetrahydrosalen synthesis from Mannich-type bases
Rivera, Augusto,Quevedo, Rodolfo,Navarro, Miguel A.,Maldonado, Mauricio
, p. 2479 - 2485 (2004)
Synthesizing a variety of tetrahydrosalens from hydrolyzing 1,3-bis (2′-hydroxy-5′-substituted-benzyl)imidazolidines with hydrochloric acid is described. Further reaction of such tetrahydrosalens with aldehydes yielded 2-substituted-1,3-bis(2′-hydroxy-5′-substituted-benzyl) imidazolidines.
Enhancing single-molecule magnet behaviour through decorating terminal ligands in Dy2 compounds
Ma, Xiufang,Chen, Bingbing,Zhang, Yi-Quan,Yang, Jinhui,Shi, Quan,Ma, Yulong,Liu, Xiangyu
supporting information, p. 12622 - 12631 (2019/08/26)
The utilization of two isomorphic ligands with different substituents leads to two centrosymmetric DyIII dimers, namely, [Dy2(bfbpen)2(H2O)2]·2I- (1) and [Dy2(bcbpen)2
FBXO3 INHIBITORS
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Page/Page column 58; 59, (2014/01/08)
The present application discloses benzathine and related compounds and their use as FBXO-3 inhibitors.
Solvent-free Mannich-type reaction of tetraazatricyclododecane (TATD) with phenols
Rivera, Augusto,Quevedo, Rodolfo
, p. 1416 - 1420 (2013/04/23)
Solvent-free Mannich-type reactions between the macrocyclic aminal 1,3,6,8-tetraazatricyclo [4.4.1.13,8]dodecane (TATD) and phenols indicate that the activation of the aromatic ring is critical for controlling the course of reaction. Activated
Synthesis and antimicrobial activity of N,N′-bis(2-hydroxylbenzyl)-1, 2-ethanediamine derivatives
Musa, Musiliyu A.,Khan, M. Omar F.,Aspedon, Arden,Cooperwood, John S.
experimental part, p. 165 - 170 (2011/02/23)
A series of N,N′-Bis(2-hydroxylbenzyl)-1,2-ethanediamine derivatives and its schiff bases were synthesized, characterized and screened for in vitro antimicrobial activity against Staphylococcus aureus, Pseudomonas aeruginosa and Salmonella enterica. Resul
Synthesis of 2t-substituted-1r,3c-bis(2'-hydroxy-5'-substituted-benzyl)- imidazolidines by reaction of 1,3-bis(2'-hydroxy-5'-substituted-benzyl)- imidazolidines with aromatic aldehydes
Rivera, Augusto,Leon, Juan Francisco,Rivera, Jasmin,Parra, Eva Cecilia,Purmova, Jindra,Burgueno-Tapia, Eleuterio,Joseph-Nathan, Pedro
, p. 2029 - 2040 (2007/10/03)
A one-step synthesis of 2t-substituted-1r,3c-bis(2'-hydroxy-5'-substitut ed-benzyl)-imidazolidines from 1,3-bis(2'-hydroxy-5'-substituted-benzyl)- imidazolidines and aromatic aldehydes is reported. The relative stereochemistry of the five-membered ring was evident from 1H NMR measurements combined with MMX calculations.
