First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone)

Mostrar todas las versiones(3)

Diosgeninlactone (1), a natural product from Solanum vespertilio, was stereo-selectively synthesized in high yield from 3β-hydroxy-5-androstene.

Guardado en:

Detalles Bibliográficos
Autores principales:	Bruttomesso, A.C., Gros, E.G.
Formato:	JOUR
Materias:	(20) 3beta,16beta dihydroxy 5 pregnen 20,16 carbolactone 3beta hydroxy 5 androsterone alkaloid derivative androsterone diosgenin hydroxyl group lactone sapogenin steroid unclassified drug catabolism cis isomer conference paper correlation analysis extraction fruit molecular dynamics molecular interaction molecular mechanics plant plant yield probability protein degradation protein isolation solanum vespertilio stereochemistry synthesis technique tomato vegetable
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p564_Bruttomesso
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

id	todo:paper_14203049_v5_n3_p564_Bruttomesso
record_format	dspace
spelling	todo:paper_14203049_v5_n3_p564_Bruttomesso2023-10-03T16:13:26Z First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone) Bruttomesso, A.C. Gros, E.G. (20) 3beta,16beta dihydroxy 5 pregnen 20,16 carbolactone 3beta hydroxy 5 androsterone alkaloid derivative androsterone diosgenin hydroxyl group lactone sapogenin steroid unclassified drug catabolism cis isomer conference paper correlation analysis extraction fruit molecular dynamics molecular interaction molecular mechanics plant plant yield probability protein degradation protein isolation solanum vespertilio stereochemistry synthesis technique tomato vegetable Diosgeninlactone (1), a natural product from Solanum vespertilio, was stereo-selectively synthesized in high yield from 3β-hydroxy-5-androstene. Fil:Bruttomesso, A.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Gros, E.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_p564_Bruttomesso
institution	Universidad de Buenos Aires
institution_str	I-28
repository_str	R-134
collection	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic	(20) 3beta,16beta dihydroxy 5 pregnen 20,16 carbolactone 3beta hydroxy 5 androsterone alkaloid derivative androsterone diosgenin hydroxyl group lactone sapogenin steroid unclassified drug catabolism cis isomer conference paper correlation analysis extraction fruit molecular dynamics molecular interaction molecular mechanics plant plant yield probability protein degradation protein isolation solanum vespertilio stereochemistry synthesis technique tomato vegetable
spellingShingle	(20) 3beta,16beta dihydroxy 5 pregnen 20,16 carbolactone 3beta hydroxy 5 androsterone alkaloid derivative androsterone diosgenin hydroxyl group lactone sapogenin steroid unclassified drug catabolism cis isomer conference paper correlation analysis extraction fruit molecular dynamics molecular interaction molecular mechanics plant plant yield probability protein degradation protein isolation solanum vespertilio stereochemistry synthesis technique tomato vegetable Bruttomesso, A.C. Gros, E.G. First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone)
topic_facet	(20) 3beta,16beta dihydroxy 5 pregnen 20,16 carbolactone 3beta hydroxy 5 androsterone alkaloid derivative androsterone diosgenin hydroxyl group lactone sapogenin steroid unclassified drug catabolism cis isomer conference paper correlation analysis extraction fruit molecular dynamics molecular interaction molecular mechanics plant plant yield probability protein degradation protein isolation solanum vespertilio stereochemistry synthesis technique tomato vegetable
description	Diosgeninlactone (1), a natural product from Solanum vespertilio, was stereo-selectively synthesized in high yield from 3β-hydroxy-5-androstene.
format	JOUR
author	Bruttomesso, A.C. Gros, E.G.
author_facet	Bruttomesso, A.C. Gros, E.G.
author_sort	Bruttomesso, A.C.
title	First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone)
title_short	First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone)
title_full	First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone)
title_fullStr	First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone)
title_full_unstemmed	First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone)
title_sort	first synthesis of (20s) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone)
url	http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p564_Bruttomesso
work_keys_str_mv	AT bruttomessoac firstsynthesisof20s3b16bdihydroxy5pregnen2016carbolactonediosgeninlactone AT groseg firstsynthesisof20s3b16bdihydroxy5pregnen2016carbolactonediosgeninlactone
_version_	1807321750777626624

First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone)

Ejemplares similares