A Novel Dendrobine‐Derived Phase‐Transfer Catalyst

Abstract The development of novel and efficient chiral catalysts has always been a focus of research in the field of organic synthesis. In this paper, we present the design, synthesis, and application of a new chiral phase‐transfer catalyst derived from Dendrobine alkaloid using simple synthetic methods with competitive yields. Meanwhile, the unique chiral skeleton structure of our catalyst was conducive to chiral induction in asymmetric catalysis and has been successfully utilized in the asymmetric alkylation of β ‐keto esters, leading to excellent reactivity and good enantioselectivity in the formation of chiral 1H‐inden‐1‐ones.

Authors

Institutions

Publication Details

Journal
ChemistrySelect
Published
2024-12-30
DOI
https://doi.org/10.1002/slct.202405664
Citations
1
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
0.25

Funders

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

A Novel Dendrobine‐Derived Phase‐Transfer Catalyst

Jiang‐Miao Hu, Shulin Ge, Yijun Liu, Shuo Chen et al.
1 citations
ChemistrySelect
Axial and Atropisomeric Chirality Synthesis
0.25
article

A Novel Dendrobine‐Derived Phase‐Transfer Catalyst

Jiang‐Miao Hu, Shulin Ge, Yijun Liu, Shuo Chen, Xiaojiang Shen, Fa-Wu Dong
article en
1 citations

Abstract

Abstract The development of novel and efficient chiral catalysts has always been a focus of research in the field of organic synthesis. In this paper, we present the design, synthesis, and application of a new chiral phase‐transfer catalyst derived from Dendrobine alkaloid using simple synthetic methods with competitive yields. Meanwhile, the unique chiral skeleton structure of our catalyst was conducive to chiral induction in asymmetric catalysis and has been successfully utilized in the asymmetric alkylation of β ‐keto esters, leading to excellent reactivity and good enantioselectivity in the formation of chiral 1H‐inden‐1‐ones.

ChemistrySelectVol. 10(1)
Kunming Institute of Botany (CN), Yunnan Agricultural University (CN), Chinese Academy of Sciences (CN), Yunnan University of Traditional Chinese Medicine (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 45%
Axial and Atropisomeric Chirality Synthesis
0.25
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.