875542-94-2Relevant articles and documents
Synthesis and anticancer activity of conformationally constrained Smac mimetics containing pseudo β turns
Baravkar, Sachin B.,Wagh, Mahendra A.,Paul, Debasish,Santra, Manas,Sanjayan, Gangadhar J.
, p. 3473 - 3476 (2018/08/24)
Herein, we report synthesis and in vitro anticancer activity of conformationally constrained Smac mimetics containing reverse turn inducing motifs “Ant-Pro” and “sAnt-Pro”. The synthesis of Smac analogs with diverse hydrophobic groups at the C-
Proline imidazolidinones and enamines in Hajos-Wiechert and Wieland-Miescher ketone synthesis
de Arriba, ángel L. Fuentes,Simón, Luis,Raposo, César,Alcázar, Victoria,Morán, Joaquín R.
experimental part, p. 4841 - 4845 (2009/10/02)
Readily available aromatic prolinamides obtained from the acid chloride of proline hydrochloride and anilines induce large enantiomeric excesses in intramolecular aldol condensations. Imidazolidinones derived from the reaction of the catalyst and enamines