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:
Autores principales: | , , |
---|---|
Formato: | JOUR |
Materias: | |
Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p447_DiChenna |
Aporte de: |
id |
todo:paper_14203049_v5_n3_p447_DiChenna |
---|---|
record_format |
dspace |
spelling |
todo:paper_14203049_v5_n3_p447_DiChenna2023-10-03T16:13:20Z Synthesis of D-homo analogs of neurosteroids 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. JOUR 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) |
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 |
JOUR |
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 |
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_ |
1807316088919162880 |