Electron-transfer chain-substitution in hydrodemercuration of alkylmercury(II) compounds with n-benzyl-1,4-dihydronicotinamide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. 1-Benzyl-1,4-dihydronicotinamide as a reagent for replacing aliphatic nitro groups by hydrogen: an electron-transfer chain reaction
2. Chemistry of dihydropyridines. 9. Hydride transfer from 1,4-dihydropyridines to sp3-hybridized carbon in sulfonium salts and activated halides. Studies with NAD(P)H models
3. Neighbouring-group effects in the oxidation of olefins by mercury(II), thallium(III), and lead(IV) acetates
4. H. Kurosawa and H. Okada, unpublished results.
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2. Synthesis of γ-disubstituted nitroalkyl compounds through a new solvomercuration-SRN1 reaction sequence;Arkivoc;2005-11-18
3. Reactions of 1-haloadamantanes and ethylmercury chloride with nitronate anions by the SRN1 mechanism;New Journal of Chemistry;2005
4. One or More CH Bond(s) Formed by Substitution: Reduction of CarbonNitrogen, Phosphorus, Arsenic, Antimony, Bismuth, Carbon, Boron, and Metal Bonds;Comprehensive Organic Functional Group Transformations II;2005
5. Mechanism of Photoinduced Reactions between 1-Acetylisatin and Aldehydes;European Journal of Organic Chemistry;2004-02
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