Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates
Prechter A, Gröger H, Heinrich MR. Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates. Organic & Biomolecular Chemistry . 2012;10(17): 3384. The kinetic enzymatic resolution of azo acetates via aminolysis with Candida antarctica lipase B has been investigated us...
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ftubbiepub:oai:pub.uni-bielefeld.de:2490875 2023-05-15T13:40:40+02:00 Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates Prechter, Agnes Gröger, Harald Heinrich, Markus R 2012 https://pub.uni-bielefeld.de/record/2490875 eng eng Royal Society of Chemistry (RSC) info:eu-repo/semantics/altIdentifier/doi/10.1039/c2ob25247c info:eu-repo/semantics/altIdentifier/issn/1477-0520 info:eu-repo/semantics/altIdentifier/issn/1477-0539 info:eu-repo/semantics/altIdentifier/wos/000302420700003 info:eu-repo/semantics/altIdentifier/pmid/22441297 https://pub.uni-bielefeld.de/record/2490875 info:eu-repo/semantics/closedAccess http://purl.org/coar/resource_type/c_6501 info:eu-repo/semantics/article doc-type:article text 2012 ftubbiepub https://doi.org/10.1039/c2ob25247c 2022-02-08T22:32:46Z Prechter A, Gröger H, Heinrich MR. Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates. Organic & Biomolecular Chemistry . 2012;10(17): 3384. The kinetic enzymatic resolution of azo acetates via aminolysis with Candida antarctica lipase B has been investigated using benzylamine as amine component. The products obtained from this biotransformation in high enantiomeric purity can serve as valuable precursors for various amino alcohols, as exemplified by the synthesis of the serotonin reuptake inhibitor (S)-(+)-cericlamine. Article in Journal/Newspaper Antarc* Antarctica PUB - Publications at Bielefeld University Organic & Biomolecular Chemistry 10 17 3384 |
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Open Polar |
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PUB - Publications at Bielefeld University |
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ftubbiepub |
language |
English |
description |
Prechter A, Gröger H, Heinrich MR. Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates. Organic & Biomolecular Chemistry . 2012;10(17): 3384. The kinetic enzymatic resolution of azo acetates via aminolysis with Candida antarctica lipase B has been investigated using benzylamine as amine component. The products obtained from this biotransformation in high enantiomeric purity can serve as valuable precursors for various amino alcohols, as exemplified by the synthesis of the serotonin reuptake inhibitor (S)-(+)-cericlamine. |
format |
Article in Journal/Newspaper |
author |
Prechter, Agnes Gröger, Harald Heinrich, Markus R |
spellingShingle |
Prechter, Agnes Gröger, Harald Heinrich, Markus R Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates |
author_facet |
Prechter, Agnes Gröger, Harald Heinrich, Markus R |
author_sort |
Prechter, Agnes |
title |
Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates |
title_short |
Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates |
title_full |
Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates |
title_fullStr |
Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates |
title_full_unstemmed |
Synthesis of (S)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates |
title_sort |
synthesis of (s)-(+)-cericlamine through lipase-catalyzed aminolysis of azo acetates |
publisher |
Royal Society of Chemistry (RSC) |
publishDate |
2012 |
url |
https://pub.uni-bielefeld.de/record/2490875 |
genre |
Antarc* Antarctica |
genre_facet |
Antarc* Antarctica |
op_relation |
info:eu-repo/semantics/altIdentifier/doi/10.1039/c2ob25247c info:eu-repo/semantics/altIdentifier/issn/1477-0520 info:eu-repo/semantics/altIdentifier/issn/1477-0539 info:eu-repo/semantics/altIdentifier/wos/000302420700003 info:eu-repo/semantics/altIdentifier/pmid/22441297 https://pub.uni-bielefeld.de/record/2490875 |
op_rights |
info:eu-repo/semantics/closedAccess |
op_doi |
https://doi.org/10.1039/c2ob25247c |
container_title |
Organic & Biomolecular Chemistry |
container_volume |
10 |
container_issue |
17 |
container_start_page |
3384 |
_version_ |
1766138306820571136 |