High‐Throughput Synthesis and Analysis of Acylated Cyanohydrins

Abstract The yields and optical purities of products obtained from chiral Lewis acid/Lewis base‐catalysed additions of α‐ketonitriles to prochiral aldehydes could be accurately determined by an enzymatic method. The amount of remaining aldehyde was determined after its reduction to an alcohol, whils...

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Published in:Chemistry – A European Journal
Main Authors: Hamberg, Anders, Lundgren, Stina, Wingstrand, Erica, Moberg, Christina, Hult, Karl
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2007
Subjects:
Online Access:http://dx.doi.org/10.1002/chem.200601638
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spelling crwiley:10.1002/chem.200601638 2024-09-30T14:24:55+00:00 High‐Throughput Synthesis and Analysis of Acylated Cyanohydrins Hamberg, Anders Lundgren, Stina Wingstrand, Erica Moberg, Christina Hult, Karl 2007 http://dx.doi.org/10.1002/chem.200601638 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchem.200601638 https://onlinelibrary.wiley.com/doi/full/10.1002/chem.200601638 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Chemistry – A European Journal volume 13, issue 15, page 4334-4341 ISSN 0947-6539 1521-3765 journal-article 2007 crwiley https://doi.org/10.1002/chem.200601638 2024-09-17T04:51:56Z Abstract The yields and optical purities of products obtained from chiral Lewis acid/Lewis base‐catalysed additions of α‐ketonitriles to prochiral aldehydes could be accurately determined by an enzymatic method. The amount of remaining aldehyde was determined after its reduction to an alcohol, whilst the two product enantiomers were analysed after subsequent hydrolysis first by the ( S )‐selective Candida antarctica lipase B and then by the unselective pig liver esterase. The method could be used for analysis of products obtained from a number of aromatic aldehydes and aliphatic ketonitriles. Microreactor technology was successfully combined with high‐throughput analysis for efficient catalyst optimization. Article in Journal/Newspaper Antarc* Antarctica Wiley Online Library Chemistry – A European Journal 13 15 4334 4341
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Abstract The yields and optical purities of products obtained from chiral Lewis acid/Lewis base‐catalysed additions of α‐ketonitriles to prochiral aldehydes could be accurately determined by an enzymatic method. The amount of remaining aldehyde was determined after its reduction to an alcohol, whilst the two product enantiomers were analysed after subsequent hydrolysis first by the ( S )‐selective Candida antarctica lipase B and then by the unselective pig liver esterase. The method could be used for analysis of products obtained from a number of aromatic aldehydes and aliphatic ketonitriles. Microreactor technology was successfully combined with high‐throughput analysis for efficient catalyst optimization.
format Article in Journal/Newspaper
author Hamberg, Anders
Lundgren, Stina
Wingstrand, Erica
Moberg, Christina
Hult, Karl
spellingShingle Hamberg, Anders
Lundgren, Stina
Wingstrand, Erica
Moberg, Christina
Hult, Karl
High‐Throughput Synthesis and Analysis of Acylated Cyanohydrins
author_facet Hamberg, Anders
Lundgren, Stina
Wingstrand, Erica
Moberg, Christina
Hult, Karl
author_sort Hamberg, Anders
title High‐Throughput Synthesis and Analysis of Acylated Cyanohydrins
title_short High‐Throughput Synthesis and Analysis of Acylated Cyanohydrins
title_full High‐Throughput Synthesis and Analysis of Acylated Cyanohydrins
title_fullStr High‐Throughput Synthesis and Analysis of Acylated Cyanohydrins
title_full_unstemmed High‐Throughput Synthesis and Analysis of Acylated Cyanohydrins
title_sort high‐throughput synthesis and analysis of acylated cyanohydrins
publisher Wiley
publishDate 2007
url http://dx.doi.org/10.1002/chem.200601638
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchem.200601638
https://onlinelibrary.wiley.com/doi/full/10.1002/chem.200601638
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source Chemistry – A European Journal
volume 13, issue 15, page 4334-4341
ISSN 0947-6539 1521-3765
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1002/chem.200601638
container_title Chemistry – A European Journal
container_volume 13
container_issue 15
container_start_page 4334
op_container_end_page 4341
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