Ultrasounds in Synthetic Reactions. III. Reduction of Organic Halides with Nickel(II) Chloride–Zinc–Water
- 1 September 1985
- journal article
- research article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 58 (9) , 2709-2710
- https://doi.org/10.1246/bcsj.58.2709
Abstract
The reductive dehalogenation of aryl chlorides as well as other organic halides was facilitated with nickel(II) chloride–zinc–water in hexamethylphosphoric triamide irradiated with ultrasound.Keywords
This publication has 8 references indexed in Scilit:
- Sonochemical activation of transition metalsJournal of the American Chemical Society, 1984
- Ultrasounds in Synthetic Reactions. II. Convenient Methylenation of Carbonyl Compounds with Zinc–DiiodomethaneBulletin of the Chemical Society of Japan, 1984
- Organic sonochemistry. Ultrasonic acceleration of the hydrosilation reactionOrganometallics, 1983
- Ultrasound in organic synthesis: cyclopropanation of olefins with zinc-diiodomethaneTetrahedron Letters, 1982
- Reduction of organic halides by water and zinc effected by nickelThe Journal of Organic Chemistry, 1982
- Reaction of aryl and vinyl halides with zerovalent nickel - preparative aspects and the synthesis of alnusoneJournal of the American Chemical Society, 1981
- The in Situ-generated Nickel(0)-catalyzed Reaction of Aryl Halides with Potassium Iodide and Zinc PowderBulletin of the Chemical Society of Japan, 1980
- Studies on selective preparation of aromatic compounds. 14. An attempt to prepare all possible deuterated phenols by the reductive dehalogenation of the corresponding halophenols with Raney alloys in an alkaline deuterium oxide solutionThe Journal of Organic Chemistry, 1978