63487-02-5Relevant academic research and scientific papers
QUINOLINE COMPOUNDS AND METHODS OF USE
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Page/Page column 127, (2008/06/13)
Compounds of Formula I, and stereoisomers, geometric isomers, tautomers, solvates, metabolites, salts and pharmaceutically acceptable prodrugs thereof, are useful for inhibiting receptor tyrosine kinases and for treating hyperproliferative disorders mediated thereby. Methods of using compounds of Formula I, and stereoisomers, geometric isomers, tautomers, solvates and pharmaceutically acceptable salts thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions are disclosed. [ Formula I]
Stereoselective synthesis of 3,6-disubstituted-3,6-dihydropyridin-2-ones as potential diketopiperazine mimetics using organocopper-mediated anti-S N2′ reactions and their use in the preparation of low-molecule CXCR4 antagonists
Niida, Ayumu,Tanigaki, Hiroaki,Inokuchi, Eriko,Sasaki, Yoshikazu,Oishi, Shinya,Ohno, Hiroaki,Tamamura, Hirokazu,Wang, Zixuan,Peiper, Stephen C.,Kitaura, Kazuo,Otaka, Akira,Fujii, Nobutaka
, p. 3942 - 3951 (2007/10/03)
Organocopper-mediated anti-SN2′ reactions of γ-phosphoryloxy-α,β-unsaturated-δ-lactams were used to prepare highly functionalized diketopiperazine mimetics. The substrate phosphates 24, 32, and 47 were prepared from a-amino acid-derived allylic
Facile access to (Z)-alkene-containing diketopiperazine mimetics utilizing organocopper-mediated anti-SN2′ reactions
Niida, Ayumu,Oishi, Shinya,Sasaki, Yoshikazu,Mizumoto, Makiko,Tamamura, Hirokazu,Fujii, Nobutaka,Otaka, Akira
, p. 4183 - 4186 (2007/10/03)
Regio- and stereoselective anti-SN2′ alkylation of γ-phosphoryloxy-α,β-unsaturated-δ-lactams with organocopper reagents allowing the preparation of N-alkylated-α,δ- substituted-β,γ-unsaturated-δ-lactams as highly functionalized diketopiperazine
