Synthesis of oxime ethers under single electron oxidation induced by radical cation tris(aryl)aminium salts: O-alkylation of oximes with n-vinyl lactams-Reference-Cited by-同舟云学术

Synthesis of oxime ethers under single electron oxidation induced by radical cation tris(aryl)aminium salts: O-alkylation of oximes with n-vinyl lactams

Published:2009-03 Issue:11 Volume:65 Page:2334-2338
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Jia Xiaodong,Wang Xiaoe,Yang Caixia,Da Yuxia,Yang Li,Liu Zhongli

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. Regioselectivity in Palladium−Indium Iodide-Mediated Allylation Reaction of Glyoxylic Oxime Ether and N-Sulfonylimine

2. An Enzyme-Bound Bisubstrate Hybrid Inhibitor of Adenylosuccinate Synthetase

3. Organometallic Reactions in Aqueous Media: Indium-Promoted Additions to 2-Pyridyl and Glyoxylic Acid Oxime Ethers

4. Reaction of α,α-Dibromo Oxime Ethers with Grignard Reagents: Alkylative Annulation Providing a Pyrimidine Core

5. Addition of Organolithiums to the (R)-O-(1-Phenylbutyl)hydroxylamine (ROPHy) Oxime of Cinnamaldehyde. Asymmetric Synthesis of α-Aminoacids

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