ReviewChemical reviews2025
Catalytic Enantioselective Methods for Synthesis of 1,2-Amino Tertiary Alcohols and Their Analogues.
Review in Chemical reviews, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 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
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Who cites it
3 citing papers in PubMed.
- Cobalt-Catalyzed Radical Ligand Transfer (RLT) Enables Remote-Markovnikov Hydroamination of Alkenes.Angewandte Chemie (International ed. in English) · 2026Article
- Stereoretentive decarbonylative C(spNature · 2026Article
- Copper-Catalyzed Asymmetric Amino Lactonization of Alkenes: Direct Access to Enantioenriched 1,2-Alkylamino Alcohol Derivatives.Journal of the American Chemical Society · 2026Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
Vicinal amino alcohols, also called 1,2- or β-amino alcohols, are an important class of chemical modalities that may serve as chiral ligands for metal-based catalysts or as catalysts themselves and are found within numerous pharmaceutically active compounds. As such, a multitude of strategies have been adopted for their preparation, with traditional approaches leveraging diastereoselective synthesis of this scaffold based upon existing stereochemistry within a substrate. Many times, naturally occurring chiral variants or syntheses of the moiety from chiral natural sources have been utilized. Given their prominence, there have been myriad strategies developed for the catalytic enantioselective synthesis of β-amino alcohols; however, these have largely focused on the formation of
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Registered trials
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