Highly asymmetric aldol reaction of cyclohexanone and aromatic aldehydes catalyzed by bifunctional cyclohexane derived thiourea organocatalyst
Journal: Asian Journal of Green Chemistry (Vol.3, No. 2)Publication Date: 2019-04-01
Authors : Hanmant M. Kasralikar; Suresh C. Jadhavar; Sudhakar R. Bhusare;
Page : 201-215
Keywords : Asymmetric synthesis; Thiourea organocatalyst; Aldol reaction;
Abstract
Novel two L-proline analogues as thiourea organocatalysts were synthesised, first is the assembly of a structurally well-defined cyclohexane scaffold with a thiourea moieties and amine functionalities could constitute a new class of organocatalysts. Second is the triazole-3-thione analogue. The first one found to be efficient catalysts for the direct asymmetric aldol reaction between ketone and aromatic aldehydes. The catalysts exhibited high catalytic activity, diastereoselectivity and excellent enantioselectivity at room temperature with a low loading.
Other Latest Articles
- A review on plant extract mediated biogenic synthesis of CdO nanoparticles and their recent applications
- Removal of ammonium ions from aqueous solution using hydroxy-sodalite zeolite
- Perovskite photovoltaic nanostructured materials: device architectural design, challenges and recent progress
- Water extract of onion catalyzed Knoevenagel condensation reaction: an efficient green procedure for synthesis of α-cyanoacrylonitriles and α-cyanoacrylates
- Benign synthesis of 5-substituted 1H-tetrazoles via [3+2] cycloaddition of nitriles and sodium azide employing SO3H-carbon as an efficient heterogeneous catalyst
Last modified: 2018-12-09 05:54:20