Peer-reviewedCC BY 4.0ACS Omega
Rapid Aryne-Enabled Aryl Functionalization via Mechanically Assisted Microscale Mixing
- 1Institute of Applied Synthetic Chemistry, TU Wien , Getreidemarkt 9/163 , ,
Abstract
Herein, we demonstrate that arynes can be generated and trapped efficiently through mechanically assisted microscale mixing on a standard vortex mixer. Brief vortex agitation enables ultra-fast generation and interception of these highly reactive intermediates with N-, O-, S-, and C-nucleophiles within 1 min, therefore providing a low-energy-solvent minimized approach for aryl functionalization without the need for inert atmosphere, heating, or bulk solvent.
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BibTeX
@article{breinsperger2026rapid,
title = {{Rapid Aryne-Enabled Aryl Functionalization via Mechanically Assisted Microscale Mixing}},
author = {Johanna Breinsperger and Maximilian Kaiser and Michael Schnürch},
journal = {ACS Omega},
year = {2026},
month = sep,
doi = {10.1021/acsomega.6c09456},
url = {https://pubs.acs.org/acsodf/article/11/40/62275/5442165/Rapid-Aryne-Enabled-Aryl-Functionalization-via},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Rapid Aryne-Enabled Aryl Functionalization via Mechanically Assisted Microscale Mixing
AU - Johanna Breinsperger
AU - Maximilian Kaiser
AU - Michael Schnürch
PY - 2026
DA - 2026/09/30
JO - ACS Omega
DO - 10.1021/acsomega.6c09456
UR - https://pubs.acs.org/acsodf/article/11/40/62275/5442165/Rapid-Aryne-Enabled-Aryl-Functionalization-via
AB - Herein, we demonstrate that arynes can be generated and trapped efficiently through mechanically assisted microscale mixing on a standard vortex mixer. Brief vortex agitation enables ultra-fast generation and interception of these highly reactive intermediates with N-, O-, S-, and C-nucleophiles within 1 min, therefore providing a low-energy-solvent minimized approach for aryl functionalization without the need for inert atmosphere, heating, or bulk solvent.
SN - 2470-1343
ER -