![Enantioselective synthesis of cyanohydrins catalysed by hydroxynitrile lyases – a review - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C6OB00934D Enantioselective synthesis of cyanohydrins catalysed by hydroxynitrile lyases – a review - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C6OB00934D](https://pubs.rsc.org/image/article/2016/OB/c6ob00934d/c6ob00934d-s7_hi-res.gif)
Enantioselective synthesis of cyanohydrins catalysed by hydroxynitrile lyases – a review - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C6OB00934D
![Enantioselective synthesis of cyanohydrins catalysed by hydroxynitrile lyases – a review - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C6OB00934D Enantioselective synthesis of cyanohydrins catalysed by hydroxynitrile lyases – a review - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C6OB00934D](https://pubs.rsc.org/image/article/2016/OB/c6ob00934d/c6ob00934d-s1_hi-res.gif)
Enantioselective synthesis of cyanohydrins catalysed by hydroxynitrile lyases – a review - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C6OB00934D
![Enantioselective synthesis of cyanohydrins catalysed by hydroxynitrile lyases – a review - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C6OB00934D Enantioselective synthesis of cyanohydrins catalysed by hydroxynitrile lyases – a review - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C6OB00934D](https://pubs.rsc.org/image/article/2016/OB/c6ob00934d/c6ob00934d-s8_hi-res.gif)
Enantioselective synthesis of cyanohydrins catalysed by hydroxynitrile lyases – a review - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C6OB00934D
![Short Topic: More ways to use reagents | Mitsunobu Reaction Using Acetone Cyanohydrin | TCI EUROPE N.V. Short Topic: More ways to use reagents | Mitsunobu Reaction Using Acetone Cyanohydrin | TCI EUROPE N.V.](https://www.tcichemicals.com/assets/cms-images/156-column_Fig1(E)_web.jpg)
Short Topic: More ways to use reagents | Mitsunobu Reaction Using Acetone Cyanohydrin | TCI EUROPE N.V.
![Acetone Cyanohydrin as a Source of HCN in the Cu-Catalyzed Hydrocyanation of α-Aryl Diazoacetates | The Journal of Organic Chemistry Acetone Cyanohydrin as a Source of HCN in the Cu-Catalyzed Hydrocyanation of α-Aryl Diazoacetates | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/jo100356d/asset/images/large/jo-2010-00356d_0004.jpeg)
Acetone Cyanohydrin as a Source of HCN in the Cu-Catalyzed Hydrocyanation of α-Aryl Diazoacetates | The Journal of Organic Chemistry
![Catalytic Transfer Hydration of Cyanohydrins to α-Hydroxyamides | Journal of the American Chemical Society Catalytic Transfer Hydration of Cyanohydrins to α-Hydroxyamides | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.8b12877/asset/images/large/ja-2018-128775_0002.jpeg)
Catalytic Transfer Hydration of Cyanohydrins to α-Hydroxyamides | Journal of the American Chemical Society
![Acetone cyanohydrin - 75-86-5, C4H7NO, density, melting point, boiling point, structural formula, synthesis Acetone cyanohydrin - 75-86-5, C4H7NO, density, melting point, boiling point, structural formula, synthesis](https://www.chemsynthesis.com/molimg/1/big/14/14290.gif)
Acetone cyanohydrin - 75-86-5, C4H7NO, density, melting point, boiling point, structural formula, synthesis
![Preparation of acetone cyanohydrin (2-hydroxy-2-methylpropanenitrile; 2-hydroxyisobutyronitrile; alpha-hydroxyisobutyronitrile) Preparation of acetone cyanohydrin (2-hydroxy-2-methylpropanenitrile; 2-hydroxyisobutyronitrile; alpha-hydroxyisobutyronitrile)](https://prepchem.com/uploads/7e/2a/54dedf9e52df3bdd077dcede56c8.png)
Preparation of acetone cyanohydrin (2-hydroxy-2-methylpropanenitrile; 2-hydroxyisobutyronitrile; alpha-hydroxyisobutyronitrile)
![Catalytic Transfer Hydration of Cyanohydrins to α-Hydroxyamides | Journal of the American Chemical Society Catalytic Transfer Hydration of Cyanohydrins to α-Hydroxyamides | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.8b12877/asset/images/medium/ja-2018-128775_0001.gif)