Synthesis of oxime ethers under single electron oxidation induced by radical cation tris(aryl)aminium salts: O-alkylation of oximes with n-vinyl lactams
-
Add time:09/29/2019 Source:sciencedirect.com
O-Alkylation of (E)- and (Z)-oxime was achieved via single electron oxidation of N-vinyl lactams by using a catalytic amount of tris(aryl)aminium salts as initiator, producing the corresponding oxime ethers in high yields under mild condition. A reaction mechanism based on electron transfer was proposed.
We also recommend Trading Suppliers and Manufacturers of 2-FURALDEHYDE OXIME (cas 1121-47-7). Pls Click Website Link as below: cas 1121-47-7 suppliers
Prev:A simple Ru catalyst for the conversion of aldehydes or oximes to primary amides
Next:Chapter 9 - Arylamines (Anilines), Azines, and Oximes) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Chapter 9 - Arylamines (Anilines), Azines, and Oximes09/30/2019
- A simple Ru catalyst for the conversion of aldehydes or oximes to primary amides09/28/2019
- O-Alkylation of oxime with N-vinyl lactams induced by radical cation10/01/2019
- One step from nitro to oxime: a convenient preparation of unsaturated oximes by the reduction of the corresponding vinylnitro compounds09/27/2019
- Cerium (IV) ammonium nitrate (CAN) initiated O-alkylation of oximes with N-vinyl lactams09/26/2019
- Structure-activity relationships of some 5-nitro-2-FURALDEHYDE OXIME (cas 1121-47-7)s and hydrazones09/25/2019
- Conformational stability, vibrational spectra, molecular structure, NBO and HOMO–LUMO analysis of 5-nitro-2-FURALDEHYDE OXIME (cas 1121-47-7) based on DFT calculations09/24/2019
