ReviewTopics in current chemistry (Cham)2025
Merging Multicomponent Reactions and Metal-Free C-H Functionalization: Emerging Tools in Organic Synthesis.
Review in Topics in current chemistry (Cham), 2025. 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.
- Recent advances in synthesis and medicinal chemistry of pyrrolodiazepines.Frontiers in chemistry · 2026Review
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
No grant is acknowledged in the PubMed record.
Abstract
The pursuit of metal-free multicomponent reactions (MCRs) via direct C-H bond functionalization represents a significant stride toward sustainable and atom-economical organic synthesis. This review comprehensively examines advances from 2016 to 2025 in metal-free C-H functionalization strategies integrated with MCRs for the efficient construction of complex, bioactive heterocycles. Key mechanistic platforms explored include iminium ion activation, azomethine ylide chemistry, radical-mediated transformations, visible-light photoredox catalysis, and base-mediated protocols. Each approach is critically analyzed in terms of substrate scope, regioselectivity and stereoselectivity, green metrics, and practical applicability. The strategic use of renewable feedstocks, solvent-free conditions, and recyclable catalysts further highlights the field's alignment with green chemistry principles. Collectively, these methodologies underscore the growing potential of metal-free MCRs in delivering structurally diverse heterocyclic scaffolds for pharmaceutical and materials applications.
Indexed as
Identifiers
41389179What 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.