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Divergent Synthesis of Chromones and Chromanones from Diketones Using an Agotf/[Si]H System by Switching Hydrosilanes

https://doi.org/10.2139/ssrn.4773911
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Iron‐Catalyzed Dehydrogenative Coupling of Tertiary Silanes
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Ruthenium–NHC‐Catalyzed Asymmetric Hydrogenation of Flavones and Chromones: General Access to Enantiomerically Enriched Flavanones, Flavanols, Chromanones, and Chromanols
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The synthesis of 8‐allyl‐2‐styrylchromones by the modified baker‐venkataraman transformation
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A Biologically Active Chromone from Bomarea setacea ( alstroemeriaceae ): Leishmanicidal, Antioxidant and Multilevel Computational Studies
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Health benefits of chromones: common ingredients of our daily diet
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Chromanone-A Prerogative Therapeutic Scaffold: An Overview
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Rh(1,3-bis(2,4,6-trimethylphenyl)-3,4,5,6-tetrahydropyrimidin-2-ylidene)(COD) tetrafluoroborate, an unsymmetrical Rh-homoazallylcarbene: synthesis, X-ray structure and reactivity in carbonyl arylation and hydrosilylation reactions
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Synthesis of functionalized chromones via organocatalysis
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Direct synthesis of Stryker’s reagent from a Cu(II) salt
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Synthesis of flavanones by use of anhydrous potassium carbonate as an inexpensive, safe, and efficient basic catalyst
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Stereoselective synthesis of either (E)- or (Z)-silyl enol ether from the same acyclic α,β-unsaturated ketone using cationic rhodium complex-catalyzed 1,4-hydrosilylation
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Facile Pd-catalyzed chemoselective transfer hydrogenation of olefins using formic acid in water
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Novel catalytic hydrogenolysis of silyl enol ethers by the use of acidic ruthenium dihydrogen complexes
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Chromone as a Privileged Scaffold in Drug Discovery: Recent Advances
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Diversity-Oriented Synthesis of Heterocycles: Al(OTf)3-Promoted Cascade Cyclization and Ionic Hydrogenation
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One-Pot Synthesis of O-Heterocycles or Aryl Ketones Using an InCl3/Et3SiH System by Switching the Solvent
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Silver(I)-Catalyzed Reductive Cross-Coupling of Aldehydes to Structurally Diverse Cyclic and Acyclic Ethers
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Enantioselective Protonation of Silyl Enol Ether Using Excited State Proton Transfer Dyes
inferredcites →https://doi.org/10.1021/acs.orglett.9b01055openalex-extracted
Silver-Catalyzed Reduction of Quinolines in Water
inferredcites →https://doi.org/10.1021/acscatal.6b02767openalex-extracted
Supported Palladium–Gold Alloy Catalysts for Efficient and Selective Hydrosilylation under Mild Conditions with Isolated Single Palladium Atoms in Alloy Nanoparticles as the Main Active Site
inferredcites →https://doi.org/10.1021/ja2101246openalex-extracted
Metal-Catalyzed Reduction of HCONR′2, R′ = Me (DMF), Et (DEF), by Silanes to Produce R′2NMe and Disiloxanes: A Mechanism Unraveled
inferredcites →https://doi.org/10.1021/ja806419hopenalex-extracted
Scope and Mechanism of the Iridium-Catalyzed Cleavage of Alkyl Ethers with Triethylsilane
inferredcites →https://doi.org/10.1021/jo501824zopenalex-extracted
Synthesis of Dihydrobenzoheterocycles through Al(OTf)3-Mediated Cascade Cyclization and Ionic Hydrogenation
inferredcites →https://doi.org/10.1021/jo901513vopenalex-extracted
Palladium-Catalyzed Preparation of Silyl Enolates from α,β-Unsaturated Ketones or Cyclopropyl Ketones with Hydrosilanes
inferredcites →https://doi.org/10.1039/c3cc49524hopenalex-extracted
The synergistic effect of nanoporous AuPd alloy catalysts on highly chemoselective 1,4-hydrosilylation of conjugated cyclic enones
inferredcites →https://doi.org/10.1039/c5cc08081aopenalex-extracted
Protonation of silylenol ether via excited state proton transfer catalysis
inferredcites →https://doi.org/10.1039/c7cc03939eopenalex-extracted
A highly enantioselective access to chiral chromanones and thiochromanones via copper-catalyzed asymmetric conjugated reduction of chromones and thiochromones
inferredcites →https://doi.org/10.1039/d0cc07916bopenalex-extracted
Hydrosilylation of carbonyls over electron-enriched Ni sites of intermetallic compound Ni 3 Ga heterogeneous catalyst
inferredcites →https://doi.org/10.1039/d1md00394aopenalex-extracted
Recent advancements in chromone as a privileged scaffold towards the development of small molecules for neurodegenerative therapeutics
inferredcites →https://doi.org/10.1039/d1ob01352aopenalex-extracted
Current developments in the synthesis of 4-chromanone-derived compounds
inferredcites →https://doi.org/10.1071/ch10295openalex-extracted
Efficient Synthesis of Chromones with Alkenyl Functionalities by the Heck Reaction
inferredcites →https://doi.org/10.1080/03639045.2021.2001489openalex-extracted
Structure activity evaluation and computational analysis identify potent, novel 3-benzylidene chroman-4-one analogs with anti-fungal, anti-oxidant, and anti-cancer activities
inferredcites →https://doi.org/10.1080/14786419.2019.1678618openalex-extracted
Human health-related properties of chromones: an overview
inferredcites →https://doi.org/10.1080/14786419.2022.2027936openalex-extracted
First synthetic report and antioxidant potential of natural product (±)-5,7-dihydroxy-8-methyl-3-(2',4'-dihydroxybenzyl)chroman-4-one from Chinese medicine Gan Luo Xin pill
inferredcites →https://doi.org/10.1111/cbdd.13951openalex-extracted
Chromones: Privileged scaffold in anticancer drug discovery
inferredcites →https://doi.org/10.1248/cpb.54.1622openalex-extracted
Dirhodium(II) Tetrakis(perfluorobutyrate)-Catalyzed 1,4-Hydrosilylation of .ALPHA.,.BETA.-Unsaturated Carbonyl Compounds
inferredcites →https://doi.org/10.14233/ajchem.2023.23442openalex-extracted
Synthetic Routes and Biological Activities of Chromone Scaffolds: An Overview
inferredcites →https://doi.org/10.22159/ajpcr.2018.v11i12.27960openalex-extracted
A REVIEW ON THE SYNTHETIC METHODOLOGIES OF CHROMONES
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.