Lipase-catalyzed acetylation and esterification of bile acids
In this chapter we describe the application of lipases as catalysts in reactions on a relevant family of steroids: the bile acids. Twenty three monoacetyl, diacetyl, and ester derivatives of deoxycholic, chenodeoxycholic, lithocholic, and cholic acids, 15 of them new compounds, were obtained through...
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| Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_10643745_v1835_n_p337_Baldessari |
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todo:paper_10643745_v1835_n_p337_Baldessari2023-10-03T16:01:57Z Lipase-catalyzed acetylation and esterification of bile acids Baldessari, A. García Liñares, G. Acetylation Alcoholysis Bile acids Esterification Lipases bile acid chenodeoxycholic acid deoxycholic acid lithocholic acid triacylglycerol lipase acetylation alcoholysis catalysis enzyme mechanism enzyme substrate esterification molecular docking molecular model In this chapter we describe the application of lipases as catalysts in reactions on a relevant family of steroids: the bile acids. Twenty three monoacetyl, diacetyl, and ester derivatives of deoxycholic, chenodeoxycholic, lithocholic, and cholic acids, 15 of them new compounds, were obtained through lipase-catalyzed acetylation, esterification, and alcoholysis reactions in very good to excellent yield and a highly regioselective way. Among them, acetylated ester products, in which the lipase catalyzed both reactions in one pot, were obtained. The influence of various reaction parameters in the enzymatic reactions, such as enzyme source, nucleophile/substrate ratio, enzyme/substrate ratio, solvent, and temperature, was studied. Some of the reported products are novel, and it is not possible to obtain them satisfactorily by following traditional synthetic procedures. Due to its singular structure containing three hydroxyl groups, cholic acid showed a different behavior in the enzymatic reactions, from that observed for the other three bile acids studied. In order to shed light to different behaviors of bile acids in the enzymatic reactions, molecular modeling was applied to substrates and some derivatives. © Springer Science+Business Media, LLC, part of Springer Nature 2018. SER info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_10643745_v1835_n_p337_Baldessari |
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Universidad de Buenos Aires |
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I-28 |
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R-134 |
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Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
Acetylation Alcoholysis Bile acids Esterification Lipases bile acid chenodeoxycholic acid deoxycholic acid lithocholic acid triacylglycerol lipase acetylation alcoholysis catalysis enzyme mechanism enzyme substrate esterification molecular docking molecular model |
| spellingShingle |
Acetylation Alcoholysis Bile acids Esterification Lipases bile acid chenodeoxycholic acid deoxycholic acid lithocholic acid triacylglycerol lipase acetylation alcoholysis catalysis enzyme mechanism enzyme substrate esterification molecular docking molecular model Baldessari, A. García Liñares, G. Lipase-catalyzed acetylation and esterification of bile acids |
| topic_facet |
Acetylation Alcoholysis Bile acids Esterification Lipases bile acid chenodeoxycholic acid deoxycholic acid lithocholic acid triacylglycerol lipase acetylation alcoholysis catalysis enzyme mechanism enzyme substrate esterification molecular docking molecular model |
| description |
In this chapter we describe the application of lipases as catalysts in reactions on a relevant family of steroids: the bile acids. Twenty three monoacetyl, diacetyl, and ester derivatives of deoxycholic, chenodeoxycholic, lithocholic, and cholic acids, 15 of them new compounds, were obtained through lipase-catalyzed acetylation, esterification, and alcoholysis reactions in very good to excellent yield and a highly regioselective way. Among them, acetylated ester products, in which the lipase catalyzed both reactions in one pot, were obtained. The influence of various reaction parameters in the enzymatic reactions, such as enzyme source, nucleophile/substrate ratio, enzyme/substrate ratio, solvent, and temperature, was studied. Some of the reported products are novel, and it is not possible to obtain them satisfactorily by following traditional synthetic procedures. Due to its singular structure containing three hydroxyl groups, cholic acid showed a different behavior in the enzymatic reactions, from that observed for the other three bile acids studied. In order to shed light to different behaviors of bile acids in the enzymatic reactions, molecular modeling was applied to substrates and some derivatives. © Springer Science+Business Media, LLC, part of Springer Nature 2018. |
| format |
SER |
| author |
Baldessari, A. García Liñares, G. |
| author_facet |
Baldessari, A. García Liñares, G. |
| author_sort |
Baldessari, A. |
| title |
Lipase-catalyzed acetylation and esterification of bile acids |
| title_short |
Lipase-catalyzed acetylation and esterification of bile acids |
| title_full |
Lipase-catalyzed acetylation and esterification of bile acids |
| title_fullStr |
Lipase-catalyzed acetylation and esterification of bile acids |
| title_full_unstemmed |
Lipase-catalyzed acetylation and esterification of bile acids |
| title_sort |
lipase-catalyzed acetylation and esterification of bile acids |
| url |
http://hdl.handle.net/20.500.12110/paper_10643745_v1835_n_p337_Baldessari |
| work_keys_str_mv |
AT baldessaria lipasecatalyzedacetylationandesterificationofbileacids AT garcialinaresg lipasecatalyzedacetylationandesterificationofbileacids |
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1782027631224422400 |