65833-16-1Relevant academic research and scientific papers
BINOL-fused maleimides - A new class of C2-symmetric chiral imides
Brenet, Simon,Baptiste, Benoit,Philouze, Christian,Berthiol, Florian,Einhorn, Jacques
supporting information, p. 1041 - 1045 (2013/04/23)
The first synthesis of BINOL-fused maleimides has been developed. This new chiral scaffold is easily accessible from various BINOL analogues and 2,3-dihalomaleimide derivatives under basic conditions. It can be easily functionalized on the BINOL moiety an
Development of methods for the synthesis of libraries of substituted maleimides and α,β-unsaturated-γ-butyrolactams
Awuah, Emelia,Capretta, Alfredo
experimental part, p. 3122 - 3130 (2011/06/24)
Synthetic methods for the preparation of maleimide and α,β- unsaturated-γ-butyrolactam compound collections are described. These routes take advantage of Pd cross-coupling and conjugate addition/elimination reactions to permit the facile production of bisaryl-maleimides, anilinoaryl-maleimides, and bisanilino-maleimides while allowing control over the synthesis of symmetrical or nonsymmetrical derivatives. Similarly, the chemistry developed allows for the generation of bisaryl substituted α,β-unsaturated-γ-butyrolactams. The scope and limitations of the approaches are presented.
Oxidation of 1-(4-nitrophenyl)-2-formylpyrrole
Kul'nevich,Baum,Goldovskaya
, p. 375 - 379 (2007/10/02)
Pyrrole aldehydes interact with oxidizing agents to yield products which are oxidized to different degrees. Pyrrolecarboxylic acids are formed under the influence of silver oxides, an alkaline solution of permanganate, and 2-10% sulfuric acid [1-3]. With
