Efficient Syntheses of Indolizine‐3‐Phosphonates via Pyridinium Ylide [3+2] Reactions

ABSTRACT An efficient method for the synthesis of indolizine‐3‐phosphonates has been successfully developed via a [3+2] cycloaddition reaction of phosphonate‐containing pyridinium ylides with 1,1‐dimethylthioalkenes under mild conditions. The scope of this reaction and subsequent functional group transformations was systematically investigated, providing a variety of structurally diverse phosphonate‐containing indolizines in moderate to high yields. This new methodology significantly broadens the repertoire of tools to rapidly access heterocyclic phosphonates, which are often explored for their important biological activities.

Authors

Institutions

Publication Details

Journal
ChemistrySelect
Published
2026-04-01
DOI
https://doi.org/10.1002/slct.73213
Primary Topic
Synthesis and Reactivity of Heterocycles
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Efficient Syntheses of Indolizine‐3‐Phosphonates via Pyridinium Ylide [3+2] Reactions

Yusui Bi, Jianyu Xu, Zhen‐Jie Gu, Qun Dang et al.
ChemistrySelect
Synthesis and Reactivity of Heterocycles
article

Efficient Syntheses of Indolizine‐3‐Phosphonates via Pyridinium Ylide [3+2] Reactions

Yusui Bi, Jianyu Xu, Zhen‐Jie Gu, Qun Dang, Yi‐Wen Xu, Shi‐Rui Wei
article en

Abstract

ABSTRACT An efficient method for the synthesis of indolizine‐3‐phosphonates has been successfully developed via a [3+2] cycloaddition reaction of phosphonate‐containing pyridinium ylides with 1,1‐dimethylthioalkenes under mild conditions. The scope of this reaction and subsequent functional group transformations was systematically investigated, providing a variety of structurally diverse phosphonate‐containing indolizines in moderate to high yields. This new methodology significantly broadens the repertoire of tools to rapidly access heterocyclic phosphonates, which are often explored for their important biological activities.

ChemistrySelectVol. 11(14)
Shandong University of Technology (CN), MSCI (China) (CN), Viva Biotech (China) (CN)
Openalex Percentile: Top 17%
Synthesis and Reactivity of Heterocycles
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.