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

Institutions

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

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Resin-supported peptide-catalyzed asymmetric aldol reaction of aldehydes for the synthesis of (R)-pantolactone

Tie-Ying Ding, Zhi‐Hong Du, Chao‐Shan Da, Y. Liu et al.
2 citations
Organic & Biomolecular Chemistry
Chemical Synthesis and Analysis
1.61
article

Resin-supported peptide-catalyzed asymmetric aldol reaction of aldehydes for the synthesis of (R)-pantolactone

Tie-Ying Ding, Zhi‐Hong Du, Chao‐Shan Da, Y. Liu, Tianquan Lian, Meng Yuan
article en
2 citations

Abstract

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.

Organic & Biomolecular ChemistryVol. 23(25)
Shihezi University (CN), Lanzhou University (CN)
National Natural Science Foundation of China
Clean water and sanitation
Openalex Percentile: Top 17%
Chemical Synthesis and Analysis
1.61
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Resin-supported peptide-catalyzed asymmetric aldol reaction of aldehydes for the synthesis of (<i>R</i>)-pantolactone — Tie-Ying Ding, Zhi‐Hong Du, et al. · Organic & Biomolecular Chemistry (2025) | TGRS Research Map | TGRS