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

Autores
Bruttomesso, A.C.; Gros, E.G.
Año de publicación
2000
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
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.
Fuente
Molecules 2000;5(3):564-565
Materia
(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
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/2.5/ar
Repositorio
Biblioteca Digital (UBA-FCEN)
Institución
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
OAI Identificador
paperaa:paper_14203049_v5_n3_p564_Bruttomesso
Acceder
id BDUBAFCEN_6ac44826e7baeed4a24a2f229ce0b67f
oai_identifier_str paperaa:paper_14203049_v5_n3_p564_Bruttomesso
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling 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 carbolactone3beta hydroxy 5 androsteronealkaloid derivativeandrosteronediosgeninhydroxyl grouplactonesapogeninsteroidunclassified drugcatabolismcis isomerconference papercorrelation analysisextractionfruitmolecular dynamicsmolecular interactionmolecular mechanicsplantplant yieldprobabilityprotein degradationprotein isolationsolanum vespertiliostereochemistrysynthesistechniquetomatovegetableDiosgeninlactone (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.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_p564_BruttomessoMolecules 2000;5(3):564-565reponame: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/ar2025-10-23T11:18:26Zpaperaa:paper_14203049_v5_n3_p564_BruttomessoInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-10-23 11:18:27.017Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone)
title First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone)
spellingShingle First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone)
Bruttomesso, A.C.
(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
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)
dc.creator.none.fl_str_mv Bruttomesso, A.C.
Gros, E.G.
author Bruttomesso, A.C.
author_facet Bruttomesso, A.C.
Gros, E.G.
author_role author
author2 Gros, E.G.
author2_role author
dc.subject.none.fl_str_mv (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
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
dc.description.none.fl_txt_mv 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.
description Diosgeninlactone (1), a natural product from Solanum vespertilio, was stereo-selectively synthesized in high yield from 3β-hydroxy-5-androstene.
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_p564_Bruttomesso
url http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p564_Bruttomesso
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):564-565
reponame:Biblioteca Digital (UBA-FCEN)
instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (UBA-FCEN)
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str UBA-FCEN
institution 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_ 1846784879766798336
score 12.982451

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