info:eu-repo/semantics/article
Highly stereoselective synthesis of steroidal 2,5-diketopiperazines based on isocyanide chemistry
Fecha
2009-07Registro en:
Bruttomesso, Andrea; Eiras, Javier; Ramirez, Javier Alberto; Galagovsky, Lydia Raquel; Highly stereoselective synthesis of steroidal 2,5-diketopiperazines based on isocyanide chemistry; Pergamon-Elsevier Science Ltd; Tetrahedron Letters; 50; 28; 7-2009; 4022-4024
0040-4039
CONICET Digital
CONICET
Autor
Bruttomesso, Andrea
Eiras, Javier
Ramirez, Javier Alberto
Galagovsky, Lydia Raquel
Resumen
In this Letter we report that the Ugi reaction/cyclization sequence on a steroidal 17-carboxaldehyde leads to novel steroidal 2,5-diketopiperazines with a noteworthy stereoselectivity. A wide variety in the substitution pattern in the heterocyclic moiety was easily achieved by changing the components in the Ugi reaction. © 2009 Elsevier Ltd. All rights reserved.