ArticleChemistry (Weinheim an der Bergstrasse, Germany)2026
Bayesian Optimization of Solvent-Free Thermal Amidation via Reactive Extrusion.
Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Machine learning-assisted development of a fast Mechanochemical Johnson-Corey-Chaykovsky reaction.Nature communications · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
A solvent-free thermo-mechanochemical synthesis of amides from carboxylic acids and amines, performed in an extruder, in the absence of coupling agents, additives, or catalyst is reported. A Bayesian optimization (BO) approach, incorporating an active and soft constraint, was developed, able to handle holistically various parameters (temperature, reaction time, excess of starting materials) while targeting a high conversion and sustainability. The methodology proved to be straightforward, high-yielding, sustainable, and easily adaptable to various substrates with a reduced number of experiments. It was applied to a variety of substrates, providing an easy and efficient preparation method of amides, including bioactive macamides and the active pharmaceutical ingredient (API) moclobemide. Optimized conditions facilitated the product isolation, some of them were obtained essentially pure from the extruder, others purified by extraction or crystallization. Notably, moclobemide could be synthesized at larger scale and isolated in the complete absence of organic solvent.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.