ArticleNature chemistry2020
Total synthesis of terpenes via palladium-catalysed cyclization strategy.
Article in Nature chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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
10 citing papers in PubMed.
- Review
- Methyl hexenoate and linalool emitted by hot peppers repel western flower thrips (Frankliniella occidentalis) and attract their predator (Orius laevigatus).Scientific reports · 2025Article
- Palladium-Catalyzed Site-Selective Regiodivergent Carbocyclization of Di- and Trienallenes: A Switch between Substituted Cyclohexene and Cyclobutene.Journal of the American Chemical Society · 2025Article
- Organotransition Metal Chemistry of Terpenes: Syntheses, Structures, Reactivity and Molecular Rearrangements.Molecules (Basel, Switzerland) · 2024Review
- Unified short syntheses of oxygenated tricyclic aromatic diterpenes by radical cyclization with a photoredox catalyst.Communications chemistry · 2023Article
- Sequencing palladium-catalyzed cycloisomerization cascades in a synthesis of the gelsemine core.Chemical science · 2023Article
- Use of Monoterpenes as Potential Therapeutics in Diabetes Mellitus: A Prospective Review.Advances in pharmacological and pharmaceutical sciences · 2023Review
- Biochemistry of Terpenes and Recent Advances in Plant Protection.International journal of molecular sciences · 2021Review
- Therapeutic Applications of Terpenes on Inflammatory Diseases.Frontiers in pharmacology · 2021Review
- Recent Advances in Construction of Polycyclic Natural Product Scaffolds via One-Pot Reactions Involving Alkyne Annulation.Frontiers in chemistry · 2020Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Nature's synthetic plans to construct molecules have been developed over millions of years of evolution and frequently prove to be among the most sophisticated. Mimicking nature's route can be a direct and feasible way for synthetic organic chemists to construct complicated molecules. However, lacking nature's ability to manipulate enzymes often prevents us from reproducing the same route. Modifying nature's approaches can provide a simpler synthetic alternative to access complex structural target molecules. Here we report a strategy that simplifies the synthesis of terpenes by inverting the order of nature's two-phase biosynthesis route. We first unite simple molecules into a polyfunctionalized linear polyenyne, with all the desired carbons and oxygens in the targeted places. This compound then undergoes polyenyne cycloisomerization, in the presence of all the functional groups, to give polyoxidized terpenes. The key reaction is a palladium-catalysed polyenyne cycloisomerization that not only tolerates the presence of all of the oxygen functionalities, but also is facilitated by them.
Identifiers
32231261What 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.