86165-77-7Relevant articles and documents
Near-infrared absorbing merocyanine dyes for bulk heterojunction solar cells
Buerckstuemmer, Hannah,Kronenberg, Nils M.,Meerholz, Klaus,Wuerthner, Frank
supporting information; experimental part, p. 3666 - 3669 (2010/11/04)
A series of near-infrared absorbing merocyanine dyes bearing the strong electron-accepting 2-oxo-5-dicyanomethylene-pyrrolidine unit was synthesized and applied in combination with PC61BM and PC71BM in solution-processed photoactive
Discovery of potent, highly selective, and orally bioavailable pyridine carboxamide c-Jun NH2-terminal kinase inhibitors
Zhao, Hongyu,Serby, Michael D.,Xin, Zhili,Szczepankiewicz, Bruce G.,Liu, Mei,Kosogof, Christi,Liu, Bo,Nelson, Lissa T. J.,Johnson, Eric F.,Wang, Sanyi,Pederson, Terry,Gum, Rebecca J.,Clampit, Jill E.,Haasch, Deanna L.,Abad-Zapatero, Cele,Fry, Elizabeth H.,Rondinone, Cristina,Trevillyan, James M.,Sham, Hing L.,Liu, Gang
, p. 4455 - 4458 (2007/10/03)
C-Jun NH2 terminal kinases (JNKs) are important cell signaling enzymes. JNK1 plays a central role in linking obesity and insulin resistance. JNK2 and JNK3 may be involved in inflammatory and neurological disorders, respectively. Small-molecule JNK inhibitors could be valuable tools to study the therapeutic benefits of inhibiting these enzymes and as leads for potential drugs targeting JNKs. In this report, we disclose a series of potent and highly selective JNK inhibitors with good pharmacokinetic profiles.
Self-condensation of Ethyl 3-Amino-3-ethoxypropenoate and related Reactions
Ivanov, Ivo C.,Sulay, Piroschka B.,Dantchev, Damian K.
, p. 753 - 760 (2007/10/02)
The acid-catalyzed self-condensation of the title compound 1a - the major component of the equilibrium 1a1b - yields via elimination of ethanol a mixture of pyridine, pyrimidine, and s-triazine derivatives (Scheme 1, Table1).In order to elucidate the course of this reaction, the ester 1 has been treated with CH-acids 12a, b to give 13a, b.Condensation of 1 with the ketene O,N-acetal 14 under self-condensation conditions mainly yields the substituted 4(1H)-pyridinone 8b.