34579-88-9Relevant academic research and scientific papers
Facile, one-pot synthesis of aromatic diamine-based benzoxazines and their advantages over diamines as epoxy hardeners
Chang, Sheng Lung,Lin, Ching Hsuan
, p. 2430 - 2437 (2010)
Three aromatic diamine-based benzoxazines were successfully prepared by a facile, clean, one-pot procedure from 1,4-phenylenediamine (1), 4,4'-diaminodiphenyl ether (2), and 4,4′-diaminodiphenyl methane (3), respectively. Their structures were confirmed b
Studies on structurally different benzoxazines based on diphenols and diamines: Kinetics of thermal degradation and TG-FTIR studies
Shamim Rishwana,Mahendran,Vijayakumar
, p. 74 - 87 (2015/10/28)
Structurally different bisbenzoxazines (QB, RB, pHBA-pd and mHBA-pd) are synthesized using quinol, resorcinol, p-phenylenediamine and m-phenylenediamine and are thermally cured. The thermal stability of the materials was studied using TGA. The plate like
Synthesis and biological activity of 6-alkyl/chloro-3-{4-(6-alkyl/chloro- 2H-benzo[e][1,3]oxazin-3(4H)-yl)phenyl}-3,4-dihydro-2H-benzo[e] [1,3] oxazines
Manikannan, Ramaiyan,Muthusubramanian, Shanmugam
experimental part, p. 1083 - 1087 (2010/11/16)
The efficient synthesis of symmetrical bis-benzoxazines using microwave irradiation is described and the possibility of a multicomponernt approach to the target molecule has also been explored. The antimicrobial studies on the synthesized benzoxazines have been investigated.
N,N′-bisbenzylidenebenzene-1,4-diamines and N,N′- bisbenzylidenenaphthalene-1,4-diamines as sirtuin type 2 (SIRT2) inhibitors
Kiviranta, P?ivi H.,Lepp?nen, Jukka,Kyrylenko, Sergiy,Salo, Heikki S.,Lahtela-Kakkonen, Maija,Tervo, Anu J.,Wittekindt, Carsten,Suuronen, Tiina,Kuusisto, Erkki,J?rvinen, Tomi,Salminen, Antero,Poso, Antti,Wallén, Erik A. A.
, p. 7907 - 7911 (2007/10/03)
A series of N,N′-bisbenzylidenebenzene-1,4-diamine and N,N′-bisbenzylidenenaphthalene-1,4-diamine derivatives were synthesized as inhibitors for human sirtuin type 2 (SIRT2). The design of the new compounds was based on two earlier reported hits from molecular modeling and virtual screening. The most potent compound was N,N′-bis(2-hydroxybenzylidene) benzene-1,4-diamine, which was equipotent with the most potent hit compound and well-known SIRT2 inhibitor sirtinol.
