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Efficient Enzymatic Synthesis of Carbamates in Water Using Promiscuous Esterases/Acyltransferases

  • Biocatalysis provides an attractive approach to facilitate synthetic reactions in aqueous media. Motivated by the discovery of promiscuous aminolysis activity of esterases, we exploited the esterase from Pyrobaculum calidifontis VA1 (PestE) for the synthesis of carbamates from different aliphatic, aromatic, and arylaliphatic amines and a set of carbonates such as dimethyl‐, dibenzyl‐, or diallyl carbonate. Thus, aniline and benzylamine derivatives, aliphatic and even secondary amines could be efficiently converted into the corresponding benzyloxycarbonyl (Cbz)‐ or allyloxycarbonyl (Alloc)‐protected products in bulk water, with (isolated) yields of up to 99 %.

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Metadaten
Author: Hannes MeinertORCiD, Florian OehlschlägerORCiD, Clemens CzieglerORCiD, Jan Rockstroh, Irene MarzuoliORCiD, Serena BisagniORCiD, Michael LalkORCiD, Thomas BayerORCiD, Hans IdingORCiD, Uwe T. BornscheuerORCiD
URN:urn:nbn:de:gbv:9-opus-122571
DOI:https://doi.org/10.1002/anie.202405152
ISSN:1433-7851
ISSN:1521-3773
Parent Title (English):Angewandte Chemie International Edition
Publisher:Wiley
Place of publication:Hoboken, NJ
Document Type:Article
Language:English
Date of Publication (online):2024/05/13
Date of first Publication:2024/07/14
Release Date:2025/10/22
Tag:Acyltransferase; Amine; Biocatalysis; Carbamate; Esterase
Volume:63
Issue:30
Article Number:e202405152
Page Number:6
Faculties:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie
Collections:weitere DFG-förderfähige Artikel
Licence (German):License LogoCreative Commons - Namensnennung-Nicht kommerziell-Keine Bearbeitung 4.0 International