The First Recombinant Hydroxynitrile Lyase and its Application in the Synthesis of (S)-Cyanohydrins
The cassava species Manihot esculenta provided the first recombinant hydroxynitrile lyase (MeHNL) that became accessible by overexpression in E. coli. This MeHNL catalyzes the enantioselective addition of HCN (depicted below) not only to aliphatic, aromatic, and heteroaromatic aldehydes, but also to...
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Veröffentlicht in: | Angewandte Chemie International Edition 1996-03, Vol.35 (4), p.437-439 |
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creator | Förster, Siegfried Roos, Jürgen Effenberger, Franz Wajant, Harald Sprauer, Achim |
description | The cassava species Manihot esculenta provided the first recombinant hydroxynitrile lyase (MeHNL) that became accessible by overexpression in E. coli. This MeHNL catalyzes the enantioselective addition of HCN (depicted below) not only to aliphatic, aromatic, and heteroaromatic aldehydes, but also to ketones to give (S)‐cyanohydrins in high optical yields. R alkyl, aryl, heteroaryl; R1 H, CH3. |
doi_str_mv | 10.1002/anie.199604371 |
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This MeHNL catalyzes the enantioselective addition of HCN (depicted below) not only to aliphatic, aromatic, and heteroaromatic aldehydes, but also to ketones to give (S)‐cyanohydrins in high optical yields. 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Chem. Int. Ed. Engl</addtitle><description>The cassava species Manihot esculenta provided the first recombinant hydroxynitrile lyase (MeHNL) that became accessible by overexpression in E. coli. This MeHNL catalyzes the enantioselective addition of HCN (depicted below) not only to aliphatic, aromatic, and heteroaromatic aldehydes, but also to ketones to give (S)‐cyanohydrins in high optical yields. 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Chem. Int. Ed. Engl</addtitle><date>1996-03-01</date><risdate>1996</risdate><volume>35</volume><issue>4</issue><spage>437</spage><epage>439</epage><pages>437-439</pages><issn>0570-0833</issn><eissn>1521-3773</eissn><abstract>The cassava species Manihot esculenta provided the first recombinant hydroxynitrile lyase (MeHNL) that became accessible by overexpression in E. coli. This MeHNL catalyzes the enantioselective addition of HCN (depicted below) not only to aliphatic, aromatic, and heteroaromatic aldehydes, but also to ketones to give (S)‐cyanohydrins in high optical yields. R alkyl, aryl, heteroaryl; R1 H, CH3.</abstract><cop>Zug</cop><pub>Hüthig & Wepf Verlag</pub><doi>10.1002/anie.199604371</doi><tpages>3</tpages></addata></record> |
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subjects | (S)-cyanohydrins asymmetric syntheses enzymatic catalysis lyases |
title | The First Recombinant Hydroxynitrile Lyase and its Application in the Synthesis of (S)-Cyanohydrins |
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