Synthesis of D-homo analogs of neurosteroids

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
Lenguaje:Inglés
Publicado: 2000
Materias:
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p447_DiChenna
Aporte de:
id paperaa:paper_14203049_v5_n3_p447_DiChenna
record_format dspace
spelling paperaa:paper_14203049_v5_n3_p447_DiChenna2023-06-12T16:50:03Z Synthesis of D-homo analogs of neurosteroids Molecules 2000;5(3):447-448 Di Chenna, P. Ghini, A.A. Burton, G. 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 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. Fil:Di Chenna, P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Ghini, A.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Burton, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2000 info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion application/pdf eng info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p447_DiChenna
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
language Inglés
orig_language_str_mv eng
topic 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
spellingShingle 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
Di Chenna, P.
Ghini, A.A.
Burton, G.
Synthesis of D-homo analogs of neurosteroids
topic_facet 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
description 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.
format Artículo
Artículo
publishedVersion
author Di Chenna, P.
Ghini, A.A.
Burton, G.
author_facet Di Chenna, P.
Ghini, A.A.
Burton, G.
author_sort Di Chenna, P.
title Synthesis of D-homo analogs of neurosteroids
title_short Synthesis of D-homo analogs of neurosteroids
title_full Synthesis of D-homo analogs of neurosteroids
title_fullStr Synthesis of D-homo analogs of neurosteroids
title_full_unstemmed Synthesis of D-homo analogs of neurosteroids
title_sort synthesis of d-homo analogs of neurosteroids
publishDate 2000
url http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p447_DiChenna
work_keys_str_mv AT dichennap synthesisofdhomoanalogsofneurosteroids
AT ghiniaa synthesisofdhomoanalogsofneurosteroids
AT burtong synthesisofdhomoanalogsofneurosteroids
_version_ 1769810135660625920