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.
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I28-R145-paper_14203049_v5_n3_p447_DiChenna_oai2024-08-16 Di Chenna, P. Ghini, A.A. Burton, G. 2000 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. application/pdf http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p447_DiChenna info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar Molecules 2000;5(3):447-448 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 Synthesis of D-homo analogs of neurosteroids info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14203049_v5_n3_p447_DiChenna_oai |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-145 |
collection |
Repositorio Digital de la Universidad de Buenos Aires (UBA) |
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 https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14203049_v5_n3_p447_DiChenna_oai |
work_keys_str_mv |
AT dichennap synthesisofdhomoanalogsofneurosteroids AT ghiniaa synthesisofdhomoanalogsofneurosteroids AT burtong synthesisofdhomoanalogsofneurosteroids |
_version_ |
1809356924047589376 |