New Synthesis Method of N-Alkylation of Carbazole Under Microwave Irradiation in Dry Media.
- 1 May 1997
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 27 (9) , 1553-1560
- https://doi.org/10.1080/00397919708006093
Abstract
Under microwave irradiation carbazole reacts remarkably fast with a number of alkyl halides to give N-alkyl derivatives of carbazole. The reaction were carried out with high yield by simply mixing carbazole with an alkyl halide which was adsorb on potassium carbonate.Keywords
This publication has 7 references indexed in Scilit:
- Microwave-Assisted Alkylations of Activated Methylene GroupsSynthetic Communications, 1995
- Specific activation by microwaves: myth or reality?The Journal of Organic Chemistry, 1992
- APPLICATIONS OF MICROWAVE ENERGY IN ORGANIC CHEMISTRY. A REVIEWOrganic Preparations and Procedures International, 1991
- Microwave-induced organic reaction enhancement chemistry. 2. Simplified techniquesThe Journal of Organic Chemistry, 1991
- Application of trichloroethylene in organic syntheses. V. A Modified Synthesis of DichloroacetyleneJournal für Praktische Chemie, 1989
- A novel synthesis of N-vinylcarbazoles: Reaction conditions and mechanism of the side reactionJournal of Polymer Science Part C: Polymer Letters, 1985
- Reactions of condensed N-heteroaromatic molecules. Part I. Alkylation by thallium(I) ethoxideJournal of the Chemical Society, Perkin Transactions 1, 1972