Abstract
A synthetic method for controlling the Henry reaction products from nitrostyrene to nitroalcohol in heterogeneous catalysis by a simple change of the catalytic sites in organoamine-functionalized mesoporous catalysts is reported. The synthesis resulted in either β-nitrostyrene or β-nitroalcohol by simple change of the types of amine functional groups in the amine-functionalized mesoporous catalysts from primary amines into secondary or tertiary.
| Original language | English |
|---|---|
| Pages (from-to) | 142-148 |
| Number of pages | 7 |
| Journal | Catalysis Letters |
| Volume | 126 |
| Issue number | 1-2 |
| DOIs | |
| Publication status | Published - Nov 1 2008 |
Keywords
- Amine-functionalized mesoporous materials
- Henry reaction
- Nitroalcohol
- Nitroaldol condensation
- Nitrostyrene
ASJC Scopus subject areas
- Catalysis
- Chemistry(all)
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Anan, A., Vathyam, R., Sharma, K. K., & Asefa, T. (2008). Controlled synthesis of the henry reaction products: Nitroalcohol versus nitrostyrene by a simple change of amino-groups of aminofunctionalized nanoporous catalysts. Catalysis Letters, 126(1-2), 142-148. https://doi.org/10.1007/s10562-008-9595-1