A comprehensive picture of the one-electron oxidation chemistry of enols, enolates and α-carbonyl radicals: oxidation potentials and characterization of radical intermediates-Reference-Cited by-同舟云学术

A comprehensive picture of the one-electron oxidation chemistry of enols, enolates and α-carbonyl radicals: oxidation potentials and characterization of radical intermediates

Published:2009-12 Issue:52 Volume:65 Page:10842-10855
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Schmittel Michael,Lal Mukul,Lal Rupali,Röck Maik,Langels Anja,Rappoport Zvi,Basheer Ahmad,Schlirf Jens,Deiseroth Hans-Jörg,Flörke Ulrich,Gescheidt Georg

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference137 articles.

1. Umpolung of ketones via enol radical cations

2. Stereoselective coupling of ketone and carboxylate enolates

3. One-electron oxidation of metal enolates and metal phenolates

4. Oxidative C–C bond formation in heterocyclic chemistry

5. Syntheses of 1,3-cyclopentanediones via intramolecular oxidative coupling of 3,3-disubstituted 2,4-pentanediones by means of Cu(OTf)2

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