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spelling I28-R145-paper_14203049_v5_n3_p564_Bruttomesso_oai2020-10-19 Bruttomesso, A.C. Gros, E.G. 2000 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. application/pdf http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p564_Bruttomesso info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar Molecules 2000;5(3):564-565 (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 First synthesis of (20S) 3β,16β-dihydroxy-5-pregnen-20,16- carbolactone (diosgeninlactone) info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14203049_v5_n3_p564_Bruttomesso_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 (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 Artículo
Artículo
publishedVersion
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)
publishDate 2000
url http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p564_Bruttomesso
http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14203049_v5_n3_p564_Bruttomesso_oai
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