Lipases as catalysts in synthesis of fine chemicals

The application of lipases as catalysts in the synthesis of an intermediate of alfuzosin and lapyrium chloride is described. In the first case, the one-pot procedure to obtain the intermediate involves the treatment of tetrahydrofuroic acid with ethanol in the presence of Candida antarctica lipase f...

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Language:unknown
Published: 2012
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Online Access:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10643745_v861_n_p445_Baldessari
https://hdl.handle.net/20.500.12110/paper_10643745_v861_n_p445_Baldessari
id ftunibueairesbd:paper:paper_10643745_v861_n_p445_Baldessari
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spelling ftunibueairesbd:paper:paper_10643745_v861_n_p445_Baldessari 2023-05-15T13:51:24+02:00 Lipases as catalysts in synthesis of fine chemicals 2012 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10643745_v861_n_p445_Baldessari https://hdl.handle.net/20.500.12110/paper_10643745_v861_n_p445_Baldessari unknown https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10643745_v861_n_p445_Baldessari http://hdl.handle.net/20.500.12110/paper_10643745_v861_n_p445_Baldessari Alfuzosin Esterification and aminolysis reactions Fine chemicals Lapyrium chloride Lipases acetic acid derivative biological product chloroacetic acid diamine fungal protein furan derivative lapyrium lipase B Candida antarctica pyridinium derivative quinazoline derivative triacylglycerol lipase article biocatalysis Candida chemistry green chemistry synthesis Acetic Acids Biological Agents Diamines Fungal Proteins Furans Green Chemistry Technology Lipase Pyridinium Compounds Quinazolines 2012 ftunibueairesbd https://doi.org/20.500.12110/paper_10643745_v861_n_p445_Baldessari 2023-02-16T02:09:35Z The application of lipases as catalysts in the synthesis of an intermediate of alfuzosin and lapyrium chloride is described. In the first case, the one-pot procedure to obtain the intermediate involves the treatment of tetrahydrofuroic acid with ethanol in the presence of Candida antarctica lipase followed by the addition of N-methyl-1,3-diaminopropane. In the second part of the chapter, an efficient route for large-scale preparation of lapyrium chloride is developed from chloroacetic acid in four steps, three of them enzymatic. Due to the chemoselective behavior of the lipases, both products described in the present chapter were obtained in a high degree of purity and yield, applying mild reaction conditions, and following a low environmental impact methodology. © 2012 Springer Science+Business Media New York. Other/Unknown Material Antarc* Antarctica Biblioteca Digital FCEN-UBA (Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires)
institution Open Polar
collection Biblioteca Digital FCEN-UBA (Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires)
op_collection_id ftunibueairesbd
language unknown
topic Alfuzosin
Esterification and aminolysis reactions
Fine chemicals
Lapyrium chloride
Lipases
acetic acid derivative
biological product
chloroacetic acid
diamine
fungal protein
furan derivative
lapyrium
lipase B
Candida antarctica
pyridinium derivative
quinazoline derivative
triacylglycerol lipase
article
biocatalysis
Candida
chemistry
green chemistry
synthesis
Acetic Acids
Biological Agents
Diamines
Fungal Proteins
Furans
Green Chemistry Technology
Lipase
Pyridinium Compounds
Quinazolines
spellingShingle Alfuzosin
Esterification and aminolysis reactions
Fine chemicals
Lapyrium chloride
Lipases
acetic acid derivative
biological product
chloroacetic acid
diamine
fungal protein
furan derivative
lapyrium
lipase B
Candida antarctica
pyridinium derivative
quinazoline derivative
triacylglycerol lipase
article
biocatalysis
Candida
chemistry
green chemistry
synthesis
Acetic Acids
Biological Agents
Diamines
Fungal Proteins
Furans
Green Chemistry Technology
Lipase
Pyridinium Compounds
Quinazolines
Lipases as catalysts in synthesis of fine chemicals
topic_facet Alfuzosin
Esterification and aminolysis reactions
Fine chemicals
Lapyrium chloride
Lipases
acetic acid derivative
biological product
chloroacetic acid
diamine
fungal protein
furan derivative
lapyrium
lipase B
Candida antarctica
pyridinium derivative
quinazoline derivative
triacylglycerol lipase
article
biocatalysis
Candida
chemistry
green chemistry
synthesis
Acetic Acids
Biological Agents
Diamines
Fungal Proteins
Furans
Green Chemistry Technology
Lipase
Pyridinium Compounds
Quinazolines
description The application of lipases as catalysts in the synthesis of an intermediate of alfuzosin and lapyrium chloride is described. In the first case, the one-pot procedure to obtain the intermediate involves the treatment of tetrahydrofuroic acid with ethanol in the presence of Candida antarctica lipase followed by the addition of N-methyl-1,3-diaminopropane. In the second part of the chapter, an efficient route for large-scale preparation of lapyrium chloride is developed from chloroacetic acid in four steps, three of them enzymatic. Due to the chemoselective behavior of the lipases, both products described in the present chapter were obtained in a high degree of purity and yield, applying mild reaction conditions, and following a low environmental impact methodology. © 2012 Springer Science+Business Media New York.
title Lipases as catalysts in synthesis of fine chemicals
title_short Lipases as catalysts in synthesis of fine chemicals
title_full Lipases as catalysts in synthesis of fine chemicals
title_fullStr Lipases as catalysts in synthesis of fine chemicals
title_full_unstemmed Lipases as catalysts in synthesis of fine chemicals
title_sort lipases as catalysts in synthesis of fine chemicals
publishDate 2012
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10643745_v861_n_p445_Baldessari
https://hdl.handle.net/20.500.12110/paper_10643745_v861_n_p445_Baldessari
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_relation https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10643745_v861_n_p445_Baldessari
http://hdl.handle.net/20.500.12110/paper_10643745_v861_n_p445_Baldessari
op_doi https://doi.org/20.500.12110/paper_10643745_v861_n_p445_Baldessari
_version_ 1766255255662624768