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.
Documento: | Artículo |
Título: | Synthesis of D-homo analogs of neurosteroids |
Autor: | Di Chenna, P.; Ghini, A.A.; Burton, G. |
Filiación: | Departamento de Quimica Organica, Fac. de Ciencias Exactas y Naturales, Universidad de Buenos Aires, (1428) Buenos Aires, Argentina |
Palabras clave: | 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 |
Año: | 2000 |
Volumen: | 5 |
Número: | 3 |
Página de inicio: | 447 |
Página de fin: | 448 |
DOI: | http://dx.doi.org/10.3390/50300447 |
Título revista: | Molecules |
Título revista abreviado: | Molecules |
ISSN: | 14203049 |
CODEN: | MOLEF |
CAS: | 11alpha hydroxyprogesterone, 80-75-1 |
PDF: | https://bibliotecadigital.exactas.uba.ar/download/paper/paper_14203049_v5_n3_p447_DiChenna.pdf |
Registro: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14203049_v5_n3_p447_DiChenna |