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.

Bibliographic Details
Authors: Di Chenna, P., Ghini, A.A., Burton, G.
Format: article
Status:Published version
Publication Date:2000
Country:Argentina
Institution:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
Repository:Biblioteca Digital (UBA-FCEN)
Language:English
OAI Identifier:paperaa:paper_14203049_v5_n3_p447_DiChenna
Online Access:http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p447_DiChenna
Access Level:Open access
Keyword: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
id AR_0f9182031b23f5f0fa92038dfd8fb1cd
oai_identifier_str paperaa:paper_14203049_v5_n3_p447_DiChenna
network_acronym_str AR
network_name_str Argentina
repository_id_str
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/ar2024-05-10T10:42:34Zpaperaa: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:18962024-05-10 10:42:35.174Biblioteca 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
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
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str UBA-FCEN
institution UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (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
_version_ 1799196675586129920
score 15.812429

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