ArticleJournal of the American Chemical Society2025
General Modular and Convergent Approach to Diversely Functionalized Allylic Systems.
Article in Journal of the American Chemical Society, 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.
- PotassiumACS omega · 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
Synthesis of allylic functionalized motifs forging C-O, C-C, and C-S bonds has been achieved via visible-light-induced palladium catalysis. Simple alkenes, readily available 1,1-dielectrophiles, and commercially available nucleophiles are directly coupled in a sequential manner to construct a diverse array of medicinally relevant complex molecules. Unlike the classical Tsuji-Trost reaction, this protocol eliminates the need for prefunctionalized starting materials, offering a much more general and modular approach with options for stereoselective reactions. Additionally, inherent synthetic challenges associated with oxygen-, carbon-, and sulfur-based nucleophiles are addressed, thus establishing a versatile toolkit for accessing allylic ethers, esters, sulfones, and alkylated motifs.
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.