Oxime formation from hydroxylamine and ketone: a (computational) reality check on stage one of the mechanism. | Henry Rzepa's Blog
![Catalytic Reduction of Oximes to Hydroxylamines: Current Methods, Challenges and Opportunities - Mas‐Roselló - 2022 - Chemistry – A European Journal - Wiley Online Library Catalytic Reduction of Oximes to Hydroxylamines: Current Methods, Challenges and Opportunities - Mas‐Roselló - 2022 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/bf121b24-46eb-4c2f-ac36-d36afbec099d/chem202103683-fig-0001-m.jpg)
Catalytic Reduction of Oximes to Hydroxylamines: Current Methods, Challenges and Opportunities - Mas‐Roselló - 2022 - Chemistry – A European Journal - Wiley Online Library
![Preparation of optically active amines from oximes: Yeast catalyzed selective reduction Regular Paper | Semantic Scholar Preparation of optically active amines from oximes: Yeast catalyzed selective reduction Regular Paper | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/b194cabb333ff40a87f87afa7f304c98bdbca5e4/3-Figure2-1.png)
Preparation of optically active amines from oximes: Yeast catalyzed selective reduction Regular Paper | Semantic Scholar
![Catalysts | Free Full-Text | Heterogeneous Catalysis as an Efficient Tool for Selective Hydrogenation of Oximes to Amines and Hydroxylamines Catalysts | Free Full-Text | Heterogeneous Catalysis as an Efficient Tool for Selective Hydrogenation of Oximes to Amines and Hydroxylamines](https://pub.mdpi-res.com/catalysts/catalysts-12-01614/article_deploy/html/images/catalysts-12-01614-sch008.png?1670571970)
Catalysts | Free Full-Text | Heterogeneous Catalysis as an Efficient Tool for Selective Hydrogenation of Oximes to Amines and Hydroxylamines
![D (+) - glucose reacts with hdyroxyl amine and yields and oxime . The structure of the oxime would be . D (+) - glucose reacts with hdyroxyl amine and yields and oxime . The structure of the oxime would be .](https://d10lpgp6xz60nq.cloudfront.net/web-thumb/644941627_web.png)
D (+) - glucose reacts with hdyroxyl amine and yields and oxime . The structure of the oxime would be .
Mild reductive rearrangement of oximes and oxime ethers to secondary amines with hydrosilanes catalyzed by B(C6F5)3 - Organic Chemistry Frontiers (RSC Publishing)
![Formation of oximes and hydrazones | Aldehydes and ketones | Organic chemistry | Khan Academy - YouTube Formation of oximes and hydrazones | Aldehydes and ketones | Organic chemistry | Khan Academy - YouTube](https://i.ytimg.com/vi/gSzxeL64Cn0/maxresdefault.jpg)
Formation of oximes and hydrazones | Aldehydes and ketones | Organic chemistry | Khan Academy - YouTube
![B(C6F5)3‐Catalyzed Hydrogenation of Oxime Ethers without Cleavage of the NO Bond - Mohr - 2014 - Angewandte Chemie International Edition - Wiley Online Library B(C6F5)3‐Catalyzed Hydrogenation of Oxime Ethers without Cleavage of the NO Bond - Mohr - 2014 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/f7df20e3-d049-4093-83bf-8bc321cad7cc/msch001.gif)
B(C6F5)3‐Catalyzed Hydrogenation of Oxime Ethers without Cleavage of the NO Bond - Mohr - 2014 - Angewandte Chemie International Edition - Wiley Online Library
![Asymmetric Reduction of Oxime Ethers Promoted by Chiral Spiroborate Esters with an O3BN Framework | The Journal of Organic Chemistry Asymmetric Reduction of Oxime Ethers Promoted by Chiral Spiroborate Esters with an O3BN Framework | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/jo060123n/asset/images/large/jo060123nn00001.jpeg)
Asymmetric Reduction of Oxime Ethers Promoted by Chiral Spiroborate Esters with an O3BN Framework | The Journal of Organic Chemistry
![Reduction of ketoximes to amines by catalytic transfer hydrogenation using Raney Nickel® and 2-propanol as hydrogen donor | Semantic Scholar Reduction of ketoximes to amines by catalytic transfer hydrogenation using Raney Nickel® and 2-propanol as hydrogen donor | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/50987793ea9a101464ee55d4b59ea7d533c5885a/6-FigureI-1.png)
Reduction of ketoximes to amines by catalytic transfer hydrogenation using Raney Nickel® and 2-propanol as hydrogen donor | Semantic Scholar
![Catalysts | Free Full-Text | Heterogeneous Catalysis as an Efficient Tool for Selective Hydrogenation of Oximes to Amines and Hydroxylamines Catalysts | Free Full-Text | Heterogeneous Catalysis as an Efficient Tool for Selective Hydrogenation of Oximes to Amines and Hydroxylamines](https://www.mdpi.com/catalysts/catalysts-12-01614/article_deploy/html/images/catalysts-12-01614-sch014-550.jpg)