## Abstract The use of the modified, nonvolatile, inexpensive, and safe catalyst in the Michael addition reaction with indole (I), pyrrole (VI), and thiols (VIII)/(XI) is presented.
Synthesis and application of modified silica sulfuric acid as a solid acid heterogeneous catalyst in Michael addition reactions
β Scribed by Mohammad Ali Zolfigol; Hojat Veisi; Farajollah Mohanazadeh; Alireza Sedrpoushan
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2011
- Tongue
- English
- Weight
- 380 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.659
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β¦ Synopsis
Abstract
Modified silica sulfuric acid (MSSA) as a new type of silica sulfuric acid was prepared and effectively used in the conjugate addition of indole, pyrrole, and thiols with Michael acceptors under mild conditions at room temperature. Also, MSSA was used as a catalyst for the synthesis of 1,1,3βtriβindolyl compounds in good to excellent yield at room temperature. J. Heterocyclic Chem., (2011).
π SIMILAR VOLUMES
Ξ±-Amino phosphonates were obtained in a one-pot, simple, and efficient method from the reaction between aldehyde, aniline, trialkyl phosphite, and silica sulfuric acid as a catalyst in acetonitrile at room temperature.