ArticleScience advances2022
Asymmetric synthesis of flavanols via Cu-catalyzed kinetic resolution of chromenes and their anti-inflammatory activity.
Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Substrate-Controlled Enantiodivergence in Ni-Catalyzed Access to Phosphorylated Oxindoles With Quaternary Stereocenters.Angewandte Chemie (International ed. in English) · 2026Article
- Inverse association between dietary flavonoid intake and nocturia in middle-aged and older adults from NHANES 2007-2010.Scientific reports · 2025Article
- Probiotic biofilm modified scaffolds for facilitating osteomyelitis treatment through sustained release of bacteriophage and regulated macrophage polarization.Materials today. Bio · 2025Article
- Integrated analysis of fecal microbiota and metabolomics reveals unique characteristics of asymptomatic and classic celiac disease.Frontiers in microbiology · 2025Article
- Enantio- and Regioselective Cascade Hydroboration of Methylenecyclopropanes for Facile Access to Chiral 1,3- and 1,4-Bis(boronates).Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024Article
- Effect of the type of brewing water on the sensory and physicochemical properties of light-scented and strong-scentedFood chemistry: X · 2024Article
- Asymmetric synthesis of P-stereogenic phosphindane oxides via kinetic resolution and their biological activity.Nature communications · 2024Article
- Asymmetric synthesis of chiral (thio)chromanes and exploration on their structure-activity relationship in macrophages.RSC advances · 2023Article
- An expeditious FeClChemical science · 2022Article
- Radical-Induced Cascade Annulation/Hydrocarbonylation for Construction of 2-Aryl-4Molecules (Basel, Switzerland) · 2022Article
Corrections and comments
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Authors and funding
6 authors.
Funding
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Abstract
Flavanols are privileged heterocyclic compounds in medicinal chemistry. It is notable to develop an efficient and straightforward protocol for accessing chiral flavanols with precise control of the stereocenters. Here, a highly efficient kinetic resolution of chromenes was reported via Cu-catalyzed asymmetric hydroboration. This previously unidentified approach features a one-step synthesis of chiral flavan-3-ols containing two vicinal stereogenic centers via a highly efficient kinetic resolution (
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