Multi-site thiolation enables rapid and precise synthesis of 2-pyridone thioethers

I 2 - and Ru 3 (CO) 12 /I 2 -catalyzed protocols enable tunable, regioselective multisite thiolation of 2-pyridones with disulfides, allowing access to C3-, C5-, C3,C5-, and C3,C6-thiolated products.

Authors

Institutions

Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-12-23
DOI
https://doi.org/10.1039/d5qo01352f
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Multi-site thiolation enables rapid and precise synthesis of 2-pyridone thioethers

Shuangliang Zhao, Guan Huang, Taoyuan Liang, Zhuan Zhang et al.
Organic Chemistry Frontiers
Sulfur-Based Synthesis Techniques
article

Multi-site thiolation enables rapid and precise synthesis of 2-pyridone thioethers

Shuangliang Zhao, Guan Huang, Taoyuan Liang, Zhuan Zhang, Xingchi Li
article en

Abstract

I 2 - and Ru 3 (CO) 12 /I 2 -catalyzed protocols enable tunable, regioselective multisite thiolation of 2-pyridones with disulfides, allowing access to C3-, C5-, C3,C5-, and C3,C6-thiolated products.

Organic Chemistry FrontiersVol. 13(4)
Guangxi University (CN)
Openalex Percentile: Top 33%
Sulfur-Based Synthesis Techniques
DOISourceOpenAlex
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.

Multi-site thiolation enables rapid and precise synthesis of 2-pyridone thioethers — Shuangliang Zhao, Guan Huang, et al. · Organic Chemistry Frontiers (2025) | TGRS Research Map | TGRS