ArticleInternational journal of molecular sciences2022
Stereoselective Synthesis and Application of Gibberellic Acid-Derived Aminodiols.
Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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
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.
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Who cites it
5 citing papers in PubMed.
- Article
- Stereoselective Synthesis and Antimicrobial Studies ofPharmaceuticals (Basel, Switzerland) · 2025Article
- Gibberellic Acid (GAChemistry & biodiversity · 2025Review
- Aminodiols, aminotetraols and 1,2,3-triazoles based onRSC advances · 2024Article
- Stereoselective synthesis and antiproliferative activity ofRSC medicinal chemistry · 2024Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
A series of gibberellic acid-based aminodiols was designed and synthesized from commercially available gibberellic acid. Exposure of gibberellic acid to hydrochloric acid under reflux conditions resulted in aromatization followed by rearrangement to form allo-gibberic acid. The key intermediate, ethyl allo-gibberate, was prepared according to literature methods. Epoxidation of key intermediate and subsequent ring-opening of the corresponding epoxide with different nucleophiles resulted in
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Registered trials
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