Synthesis of D-homo analogs of neurosteroids

Autores
Di Chenna, P.; Ghini, A.A.; Burton, G.
Año de publicación
2000
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
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.
Fuente
Molecules 2000;5(3):447-448
Materia
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
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/2.5/ar
Repositorio
Biblioteca Digital (UBA-FCEN)
Institución
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
OAI Identificador
paperaa:paper_14203049_v5_n3_p447_DiChenna
Acceder
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oai_identifier_str paperaa:paper_14203049_v5_n3_p447_DiChenna
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling Synthesis of D-homo analogs of neurosteroidsDi Chenna, P.Ghini, A.A.Burton, G.11alpha hydroxyprogesterone3alpha hydroxy 5alpha pregnan 20 one derivativecyclopropylketone derivativedehydropregnenolone acetateketone derivativemercury derivativeneurosteroid derivativepregnenolone derivativesteroidunclassified drugconference paperdrug structuredrug synthesisreaction analysis17(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.2000info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p447_DiChennaMolecules 2000;5(3):447-448reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-10-16T09:30:03Zpaperaa:paper_14203049_v5_n3_p447_DiChennaInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-10-16 09:30:04.997Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv Synthesis of D-homo analogs of neurosteroids
title Synthesis of D-homo analogs of neurosteroids
spellingShingle Synthesis of D-homo analogs of neurosteroids
Di Chenna, P.
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
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
dc.creator.none.fl_str_mv Di Chenna, P.
Ghini, A.A.
Burton, G.
author Di Chenna, P.
author_facet Di Chenna, P.
Ghini, A.A.
Burton, G.
author_role author
author2 Ghini, A.A.
Burton, G.
author2_role author
author
dc.subject.none.fl_str_mv 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
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
dc.description.none.fl_txt_mv 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.
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.
publishDate 2000
dc.date.none.fl_str_mv 2000
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p447_DiChenna
url http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p447_DiChenna
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/2.5/ar
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/ar
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Molecules 2000;5(3):447-448
reponame:Biblioteca Digital (UBA-FCEN)
instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (UBA-FCEN)
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str UBA-FCEN
institution UBA-FCEN
repository.name.fl_str_mv Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
repository.mail.fl_str_mv ana@bl.fcen.uba.ar
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score 12.712165

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