Lipase-catalyzed alcoholysis of 2-thioacetoxyethyl acetate

Lipase-catalyzed alcoholysis of 2-thioacetoxyethyl acetate is described. Results depended on the biocatalyst, the nucleophile and the substrate/nucleophile ratio. When the reaction of the diester was carried out with one equivalent of 1-octanol under Candida antarctica lipase catalysis, it was found...

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Bibliographic Details
Main Authors: Iglesias, Luis Emilio, Baldessari, Alicia
Language:unknown
Published: 1998
Subjects:
Argentina
Antarc*
Antarctica
Online Access:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03650375_v86_n3-6_p203_Iglesias
https://hdl.handle.net/20.500.12110/paper_03650375_v86_n3-6_p203_Iglesias
id ftunibueairesbd:paper:paper_03650375_v86_n3-6_p203_Iglesias
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spelling ftunibueairesbd:paper:paper_03650375_v86_n3-6_p203_Iglesias 2023-05-15T13:42:26+02:00 Lipase-catalyzed alcoholysis of 2-thioacetoxyethyl acetate Iglesias, Luis Emilio Baldessari, Alicia 1998 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03650375_v86_n3-6_p203_Iglesias https://hdl.handle.net/20.500.12110/paper_03650375_v86_n3-6_p203_Iglesias unknown https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03650375_v86_n3-6_p203_Iglesias http://hdl.handle.net/20.500.12110/paper_03650375_v86_n3-6_p203_Iglesias 1998 ftunibueairesbd https://doi.org/20.500.12110/paper_03650375_v86_n3-6_p203_Iglesias 2023-02-16T01:56:29Z Lipase-catalyzed alcoholysis of 2-thioacetoxyethyl acetate is described. Results depended on the biocatalyst, the nucleophile and the substrate/nucleophile ratio. When the reaction of the diester was carried out with one equivalent of 1-octanol under Candida antarctica lipase catalysis, it was found that 2-mercaptoethyl acetate is mainly obtained through S-acetyl removal. Fil:Iglesias, L.E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Baldessari, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Other/Unknown Material Antarc* Antarctica Biblioteca Digital FCEN-UBA (Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires) Argentina
institution Open Polar
collection Biblioteca Digital FCEN-UBA (Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires)
op_collection_id ftunibueairesbd
language unknown
description Lipase-catalyzed alcoholysis of 2-thioacetoxyethyl acetate is described. Results depended on the biocatalyst, the nucleophile and the substrate/nucleophile ratio. When the reaction of the diester was carried out with one equivalent of 1-octanol under Candida antarctica lipase catalysis, it was found that 2-mercaptoethyl acetate is mainly obtained through S-acetyl removal. Fil:Iglesias, L.E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Baldessari, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
author Iglesias, Luis Emilio
Baldessari, Alicia
spellingShingle Iglesias, Luis Emilio
Baldessari, Alicia
Lipase-catalyzed alcoholysis of 2-thioacetoxyethyl acetate
author_facet Iglesias, Luis Emilio
Baldessari, Alicia
author_sort Iglesias, Luis Emilio
title Lipase-catalyzed alcoholysis of 2-thioacetoxyethyl acetate
title_short Lipase-catalyzed alcoholysis of 2-thioacetoxyethyl acetate
title_full Lipase-catalyzed alcoholysis of 2-thioacetoxyethyl acetate
title_fullStr Lipase-catalyzed alcoholysis of 2-thioacetoxyethyl acetate
title_full_unstemmed Lipase-catalyzed alcoholysis of 2-thioacetoxyethyl acetate
title_sort lipase-catalyzed alcoholysis of 2-thioacetoxyethyl acetate
publishDate 1998
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03650375_v86_n3-6_p203_Iglesias
https://hdl.handle.net/20.500.12110/paper_03650375_v86_n3-6_p203_Iglesias
geographic Argentina
geographic_facet Argentina
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_relation https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03650375_v86_n3-6_p203_Iglesias
http://hdl.handle.net/20.500.12110/paper_03650375_v86_n3-6_p203_Iglesias
op_doi https://doi.org/20.500.12110/paper_03650375_v86_n3-6_p203_Iglesias
_version_ 1766167707209695232

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