A novel and green method for the synthesis of highly substituted isoquinoline derivatives in ionic liquid
β Scribed by Xiang-Shan Wang; Jian-Rong Wu; Qing Li; Mei-Mei Zhang
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2009
- Tongue
- English
- Weight
- 121 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.244
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
magnified image A series of new highly substituted isoquinoline derivatives was obtained from the reaction of 2β(1βsubstituted piperidinβ4βylidene)malononitrile, benzaldehyde and malononitrile or cyanoacetate in ionic liquid at 50Β°C. This novel procedure was different from the previous method in the synthesis of isoquinoline using pyridine fragment as reactant to construct benzene ring, and as well as had the advantages of oneβpot, mild and environmentally benign. A possible mechanism was proposed based on the further experimental results. J. Heterocyclic Chem., (2009).
π SIMILAR VOLUMES
## Abstract Controlling the pH value by changing the negative ion of ionic liquids, the same reactions of aromatic aldehyde, 2β(2,3βdihydrothiochromenβ4βylidene) malononitrile and malononitrile product unaromatized and aromatized 6__H__βbenzo[__c__]thiochromene derivatives in high yields. The nice
## Abstract The yields depend on both the anion and the carbonate reactivity.