Synapse
⌘+K
Synapse
PulseExploreJournal ClubResearchersJournals
Instagram
HomeJournal ClubExplore
May 9, 2026Angewandte Chemie International Edition

Outside Back Cover: Millisecond Aliphatic Iodonium‐Claisen Rearrangement Enabling Dual Functionalization of Alkenyl Iodanes

View Full Paper
Ask AI
Bookmark
Share

Authors

XHXin HuangJJJiangtao JiBLBingjie Liu

Discussion

Loading...

Member takes

Overview

Research Article demonstrates a unique rearrangement method enabling dual functionalization of alkenyl iodanes at low temperatures.

Key Points

  • Investigate an aliphatic iodonium-Claisen rearrangement that allows for dual functionalization.
  • Utilized a novel iodonium-Claisen rearrangement at −78 °C
  • Achieved a reaction completion time within 74 ms
  • Focused on the stability of iodonium intermediates
  • Successfully formed and intercepted highly unstable iodonium intermediates.
  • Enabled dual functionalization of alkenyl iodanes through rapid reaction conditions.

Cite This Study

Huang et al. (2026) studied this question.

synapsesocial.com/papers/69fed16ab9154b0b82878be5https://doi.org/10.1002/anie.2026-m2904060300
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Millisecond Aliphatic Iodonium‐Claisen Rearrangement Enabling Dual Functionalization of Alkenyl Iodanes2026
  2. 2Millisecond Aliphatic Iodonium‐Claisen Rearrangement Enabling Dual Functionalization of Alkenyl Iodanes2026
  3. 3Reductive <i>ortho</i>-Cyanomethylation of Aryl Iodanes with MeCN via One-pot Iodonium-Claisen Rearrangement2025
  4. 4Chromium-Catalyzed Reductive Alkenylation and Alkylation of Aryl Iodides2026
  5. 5Rhodium-Catalyzed Difunctionalization of Alkenes Using Cyclic 1,3-Dicarbonyl-Derived Iodonium Ylides2024 · 12 citations