IQUIR   05412
INSTITUTO DE QUIMICA ROSARIO
Unidad Ejecutora - UE
artículos
Título:
An efficient approach toward the synthesis of the A/B rings of ouabain
Autor/es:
MARÍA FERNANDA PLANO; GUILLERMO R. LABADIE; MANUEL GONZALEZ SIERRA; RAQUEL M. CRAVERO
Revista:
TETRAHEDRON LETTERS
Editorial:
Elsevier
Referencias:
Año: 2006 vol. 47 p. 7447 - 7449
ISSN:
0040-4039
Resumen:
The synthesis of the highly functionalized A/B ring related to ouabain has been accomplished efficiently from commercially available α-tetralone. A key Birch reductive alkylation allows the building of an angularly substituted decalone that was adequately functionalized to produce the intermediate 2c.