86162-58-5Relevant academic research and scientific papers
Ortho Substituent Effects in Amide Hydrolysis of Maleanilic Acid Derivatives. Stabilization of Positive Charge Developed in the Transition State
Suh, Junghun,Kim, Mahn Joo,Kim, Chong Bok
, p. 2453 - 2456 (1983)
The effects of ortho substituents on the rate of the hydrolysis of maleanilic acid derivatives have been studied.The rate is enhanced up to 55 times by polar substituents, while it is retarded greatly by nonpolar substituents.The acceleration by the polar
DABCO-catalyzed [3+2] cycloaddition reactions of azomethine imines with N-aryl maleimides: Facile access to dinitrogen-fused heterocycles
Jia, Qianfa,Chen, Lei,Yang, Gongming,Wang, Jian,Wei, Jia,Du, Zhiyun
supporting information, p. 7150 - 7153 (2015/12/12)
DABCO-catalyzed [3+2] cycloaddition of azomethine imines with maleimides has been developed. This method could efficiently furnish dinitrogen-fused tetracyclic heterocycles in high levels of regioselectivity and with good yields.
N-arylmaleimide derivatives
Miller, Christopher W.,Hoyle, Charles E.,Valente, Edward J.,Zubkowski, Jeffrey D.,Joensson, E. Sonny
, p. 563 - 571 (2007/10/03)
Nine phenyl substituted N-phenylmaleimide monomers for photopolymerization studies have been characterized by x-ray crystallography. Structures for N-(2′-t-butylphenyl)maleimide (1), P21/n, a = 10.197(3) A, b = 11.904(4) A, c = 10.496(5) A, β =
