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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Autores principales: Di Chenna, P., Ghini, A.A., Burton, G.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p447_DiChenna
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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
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