Synthesis of D-homo analogs of neurosteroids

Mostrar todas las versiones(3)

17(13→18)-Abeo and D-homo analogs of the natural neurosteroid 3α-hydroxy-5αH-pregnan-20-one were prepared by anionic or radical (mercury (II) hydride mediated) rearrangements of steroidal cyclopropylketones respectively.

Guardado en:

Detalles Bibliográficos
Autores principales:	Di Chenna, P., Ghini, A.A., Burton, G.
Formato:	Artículo publishedVersion
Publicado:	2000
Materias:	11alpha hydroxyprogesterone 3alpha hydroxy 5alpha pregnan 20 one derivative cyclopropylketone derivative dehydropregnenolone acetate ketone derivative mercury derivative neurosteroid derivative pregnenolone derivative steroid unclassified drug conference paper drug structure drug synthesis reaction analysis
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p447_DiChenna https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14203049_v5_n3_p447_DiChenna_oai
Aporte de:	Repositorio Digital de la Universidad de Buenos Aires (UBA) de Universidad de Buenos Aires

Descripción
Sumario:	17(13→18)-Abeo and D-homo analogs of the natural neurosteroid 3α-hydroxy-5αH-pregnan-20-one were prepared by anionic or radical (mercury (II) hydride mediated) rearrangements of steroidal cyclopropylketones respectively.