ArticleOrganic letters2026
Stereoselective Synthesis and Functionalization of Acetylenic Boronic Esters.
Article in Organic letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hydrozirconation of homopropargyl boronic esters, readily available by Matteson homologation, allows their selective functionalization while preserving the boronic ester functionality. Metal-halogen exchange yields reactive vinyl iodides, which can be further converted into functionalized alkenes via Negishi couplings and Heck reactions. These reactions are used to generate polyketide-like structures, which are relevant for the synthesis of natural products.
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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 Socratic graph.