9-Anthraldehyde oxime: a synthetic tool for variable applications | SpringerLink
Oxime formation
Preparation of acetophenone oxime
A simple and efficient approach for preparation of hydroxylamine sulfate from the acid-catalyzed hydrolysis reaction of cyclohexanone oxime - ScienceDirect
Solved Lab 9, oxime synthesis Today, we'll be working with | Chegg.com
Oxime - Wikipedia
Synthesis of polysubstituted pyridines from oxime acetates using NH 4 I as a dual-function promoter - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C7OB02471A
Molecules | Free Full-Text | Amidoximes and Oximes: Synthesis, Structure, and Their Key Role as NO Donors
Design, Synthesis and Evaluation of Novel Isoxazolines/Oxime Sulfonates of 2′(2′,6′)-(Di)Chloropodophyllotoxins as Insecticidal Agents | Scientific Reports
File:Oxime synthesis.svg - Wikimedia Commons
Benzaldehyde oxime for synthesis 932-90-1
Organic Syntheses Procedure
FB172322 | 574-66-3 | Benzophenone oxime | Biosynth
Cyclohexanone Oxime Synthesis Notes
Solved a.) For the preparation of benzaldehyde oxime, shown | Chegg.com
Organic Syntheses Procedure
Preparation of acetone oxime
US20020123650A1 - Process for preparation of oximes and resulting products - Google Patents
Molecules | Free Full-Text | Amidoximes and Oximes: Synthesis, Structure, and Their Key Role as NO Donors
![Report: [3,3]-Rearrangements of O-Vinyl Oximes: Stereoselective Synthesis of 1,4-Dicarbonyl Compounds (56th Annual Report on Research Under Sponsorship of The American Chemical Society Petroleum Research Fund)](https://acswebcontent.acs.org/prfar/2011/images/Paper_11567_abstract_15187_0.gif "Report: [3,3]-Rearrangements of O-Vinyl Oximes: Stereoselective Synthesis of 1,4-Dicarbonyl Compounds (56th Annual Report on Research Under Sponsorship of The American Chemical Society Petroleum Research Fund)")
Report: [3,3]-Rearrangements of O-Vinyl Oximes: Stereoselective Synthesis of 1,4-Dicarbonyl Compounds (56th Annual Report on Research Under Sponsorship of The American Chemical Society Petroleum Research Fund)
Beckmann Rearrangement
The local and natural sources in synthetic methods: the practical synthesis of aryl oximes from aryl aldehydes under catalyst-free conditions in mineral water | SpringerLink
