Resin-supported peptide-catalyzed asymmetric aldol reaction of aldehydes for the synthesis of (<i>R</i>)-pantolactone
A highly enantioselective heterogeneous cross-aldol reaction between aldehydes and glyoxylates or α-ketoaldehydes has been achieved for the first time using resin-supported peptide catalysts. This study describes the synthesis of various 1,4-dicarbonyl compounds, achieving excellent enantioselectivities and yields while using water and acetonitrile as solvents. The reaction can be conducted on a gram scale, and the polystyrene aminomethyl-supported peptide can be reused in water without losing enantioselectivity. This work enables the synthesis of (<i>R</i>)-pantolactone using only two synthetic steps.
Authors
- Tie-Ying Ding
- Zhi‐Hong Du (ORCID: https://orcid.org/0000-0002-7408-3588)
- Chao‐Shan Da (ORCID: https://orcid.org/0000-0003-1306-4348)
- Y. Liu
- Tianquan Lian (ORCID: https://orcid.org/0000-0002-8351-3690)
- Meng Yuan (ORCID: https://orcid.org/0000-0001-9917-6046)
Institutions
- Shihezi University (CN)
- Lanzhou University (CN)
Publication Details
- Journal
- Organic & Biomolecular Chemistry
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5ob00706b
- Citations
- 2
- Primary Topic
- Chemical Synthesis and Analysis
- Type
- article
- Field-Weighted Citation Impact
- 1.61
Funders
- National Natural Science Foundation of China