Improved Synthesis of Aliphatic Ketones by the Reaction of Alkylmercuric Bromides With Nickel Carbonyl in the Presence of Potassium Iodide
- 1 October 1984
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 14 (12) , 1175-1179
- https://doi.org/10.1080/00397918408059650
Abstract
An improved and convenient procedure for symmetrical aliphatic ketone synthesis is described, which employs the reaction of alkylmercuric bromides with nickel carbonyl in the presence of potassium iodide.Keywords
This publication has 7 references indexed in Scilit:
- Synthesis of β-mercuri ketones by the reaction of siloxycyclopropanes with mercuric acetate and their conversion to α-methylene ketones and γ-ketoestersTetrahedron Letters, 1980
- Addition von Aldehyden an aktivierte Doppelbindungen, XIII. Synthesen von Tri‐ und PolyketonenEuropean Journal of Inorganic Chemistry, 1977
- Further study of the reaction between zerovalent platinum complexes and organomercurials: the synthesis of stable compounds with a platinum - mercury σ-bondJournal of Organometallic Chemistry, 1976
- The reaction of organomercuric compounds with nickel carbonylTetrahedron Letters, 1971
- Organic Syntheses by Means of Metal CarbonylsSynthesis, 1971
- Novel, mercurial-based symmetrical ketone synthesisJournal of the American Chemical Society, 1968
- THE PREPARATION OF DIALKYL MERCURY COMPOUNDS FROM THE GRIGNARD REAGENT.Journal of the American Chemical Society, 1922