#nitroaldol
🌿Can deep eutectic solvents do more than just provide a greener reaction medium? Alessandro Palmieri & co-workers show that DESs can act as both solvents and promoters in the Henry reaction, delivering β-nitro alcohols⚗️
#nitroaldol

👉 buff.ly/tYj9CLz
October 23, 2026 at 7:01 AM
Alex' SQUID and EPR measurements on cobalt catalysts were now published in Org. Chem. Front. Our first paper in an org chem journal! pubs.rsc.org/en/content/a... Class-II-aldolase-mimicking Lewis acid/azolium–aryloxide catalysts in direct enantioselective nitro-aldol additions
Class-II-aldolase-mimicking polyfunctional Lewis acid/azolium–aryloxide catalysts in direct enantioselective nitro-aldol additions
The catalytic asymmetric nitroaldol reaction is a powerful tool for accessing chiral 1,2-difunctionalized motifs, and numerous catalytic systems have been reported. Despite considerable progress in ac...
pubs.rsc.org
January 2, 2026 at 8:41 AM
RRIDs were included in this Chemistry – A European Journal paper. Thanks for making your methods matter! #STMpublishing #methodsmatter #methodsmatter
Odd–Even Effects Leading to Alternating Polymerization and Macrocyclization in Nitroaldol Reaction Systems
doi.org
May 21, 2025 at 11:14 PM
Odd-even Effects Leading to Alternating Polymerization and Macrocyclization in Nitroaldol Reaction Systems

Authors: Yunchuan Qi, Mubarak Ayinla, Zhen Yang, Olof Ramstrom
DOI: 10.26434/chemrxiv-2024-nwffp
December 18, 2024 at 10:55 AM
#OpenAccess article by René Peters's team.
#UNI-STUTTGART

In this article, a novel concept for asymmetric nitroaldol additions is introduced through a polyfunctional catalyst.

doi.org/10.1039/D5QO01558H
Class-II-aldolase-mimicking polyfunctional Lewis acid/azolium–aryloxide catalysts in direct enantioselective nitro-aldol additions
The catalytic asymmetric nitroaldol reaction is a powerful tool for accessing chiral 1,2-difunctionalized motifs, and numerous catalytic systems have been reported. Despite considerable progress in ac...
doi.org
December 29, 2025 at 10:01 AM