146981-00-2Relevant academic research and scientific papers
Chimeric polymers formed from a monomer capable of free radical, oxidative and electrochemical polymerisation
Lakshmi, Dhana,Whitcombe, Michael J.,Davis, Frank,Chianella, Iva,Piletska, Elena V.,Guerreiro, Antonio,Subrahmanyam, Sreenath,Brito, Paula S.,Fowler, Steven A.,Piletsky, Sergey A.
supporting information; experimental part, p. 2759 - 2761 (2009/12/04)
A new monomer, which incorporates both aniline and methacrylamide functional groups, was shown to possess orthogonal polymerisation behaviour to produce conjugated polyaniline suitable for a wide range of applications. The Royal Society of Chemistry 2009.
1,3-Dihydro-1,3-diacetyl-2H-benzimidazol-2-one: A new versatile and selective acetylating agent
Chung, In Hwa,Cha, Ki Suk,Seo, Jae Hong,Kim, Joong Hyup,Chung, Bong Young,Kim, Choong Sup
, p. 529 - 533 (2007/10/03)
1,3-Dihydro-1,3-diacetyl-2H-benzimidazol-2-one (4, DABI) was proven to be a versatile and selective acetylating agent for amines. Selectivity and reactivity are not only superior than those of other known acetylating agents, but also products could be easily separated with excellent yield.
5-Lipoxygenase inhibitors: Synthesis and structure-activity relationships of a series of 1-aryl-2H,4H-tetrahydro-1,2,4-triazin-3-ones
Bhatia, Pramila A.,Brooks, Clint D. W.,Basha, Anwer,Ratajczyk, James D.,Gunn, Bruce P.,Bouska, Jennifer B.,Lanni, Carmine,Young, Patrick R.,Bell, Randy L.,Carter, George W.
, p. 3938 - 3950 (2007/10/03)
Synthetic routes were developed to access a variety of novel 1-aryl- 2H,4H-tetrahydro-1,2,4-triazin-3-one analogs which were evaluated as 5- lipoxygenase (5-LO) inhibitors. The parent structure, 1-phenylperhydro- 1,2,4-triazin-3-one (4), was found to be a
