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Synthesis of Pyrrolo[2,1-a]isoquinoline-Derived Diheteroaryl Sulfides through Na2S2O3/DMSO/HI-Based Sulfenylation

https://doi.org/10.2139/ssrn.6411845
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Direct Synthesis of Dihydropyrrolo[2,1‐a]Isoquinolines through FeCl3 Promoted Oxidative Aromatization
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Unsymmetrical Disulfides Synthesis via Cs2CO3‐Catalyzed Three‐Component Reaction in Water
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Transition‐Metal‐Free Synthesis of Unsymmetrical Disulfides via Three‐Component Reaction of Thiosulfonates, Thiourea and Alkyl halides
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Metal‐Free, Facile Synthesis of Sulfenylated Chromones and Indoles Promoted by an Aqueous HBr−DMSO System
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Beyond the Pummerer Reaction: Recent Developments in Thionium Ion Chemistry
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Elemental‐Sulfur‐Enabled Divergent Synthesis of Disulfides, Diselenides, and Polythiophenes from β‐CF 3 ‐1,3‐Enynes
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Recent advances in sulfenylation of C(sp3) H bond under transition metal-free conditions
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Late-Stage Halogenation of Complex Substrates with Readily Available Halogenating Reagents
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Bond-Forming and -Breaking Reactions at Sulfur(IV): Sulfoxides, Sulfonium Salts, Sulfur Ylides, and Sulfinate Salts
inferredcites →https://doi.org/10.1021/acs.joc.2c02484openalex-snapshot
Bromination of Pyrrolo[2,1- a ]isoquinolines with Acetyl Bromide and Dimethyl Sulfoxide
inferredcites →https://doi.org/10.1021/acs.joc.3c00566openalex-snapshot
AcBr/DMSO Mediated Sulfenylation of Pyrrolo[2,1-a]isoquinolines
inferredcites →https://doi.org/10.1021/acs.joc.5b01248openalex-snapshot
Copper-Catalyzed Thioetherification Reactions of Alkyl Halides, Triphenyltin Chloride, and Arylboronic Acids with Nitroarenes in the Presence of Sulfur Sources
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Ammonium Iodide Induced Nonradical Regioselective Sulfenylation of Flavones via a C–H Functionalization Process
inferredcites →https://doi.org/10.1021/acs.joc.5c00386openalex-snapshot
Oxidative Iodination of Pyrrolo[2,1-a]isoquinolines with NaI/mCPBA
inferredcites →https://doi.org/10.1021/acs.joc.7b01320openalex-snapshot
Making Flavone Thioethers Using Halides and Powdered Sulfur or Na2S2O3
inferredcites →https://doi.org/10.1021/acs.joc.7b01653openalex-snapshot
Aqueous Reaction of Alcohols, Organohalides, and Odorless Sodium Thiosulfate under Transition-Metal-Free Conditions: Synthesis of Unsymmetrical Aryl Sulfides via Dual C–S Bond Formation
inferredcites →https://doi.org/10.1021/acs.joc.8b02065openalex-snapshot
Synthesis of Benzoindolizines through 1,5-Electrocyclization/Oxidation Cascades
inferredcites →https://doi.org/10.1021/acs.joc.9b01670openalex-snapshot
Promoting Effect of Crystal Water Leading to Catalyst-Free Synthesis of Heteroaryl Thioether from Heteroaryl Chloride, Sodium Thiosulfate Pentahydrate, and Alcohol
inferredcites →https://doi.org/10.1021/cr078199mopenalex-snapshot
Lamellarins and Related Pyrrole-Derived Alkaloids from Marine Organisms
inferredcites →https://doi.org/10.1021/cr5002386openalex-snapshot
Good Partnership between Sulfur and Fluorine: Sulfur-Based Fluorination and Fluoroalkylation Reagents for Organic Synthesis
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.alpha.-Sulfenylated carbonyl compounds in organic synthesis
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Metabolites of the marine prosobranch mollusk Lamellaria sp
inferredcites →https://doi.org/10.1021/jo402586vopenalex-snapshot
Diaryl and Heteroaryl Sulfides: Synthesis via Sulfenyl Chlorides and Evaluation as Selective Anti-Breast-Cancer Agents
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Direct Cross-Coupling Access to Diverse Aromatic Sulfide: Palladium-Catalyzed Double C–S Bond Construction Using Na 2 S 2 O 3 as a Sulfurating Reagent
inferredcites →https://doi.org/10.1021/ol502381eopenalex-snapshot
Direct Synthesis of Diverse 2-Aminobenzo[b]thiophenes via Palladium-Catalyzed Carbon–Sulfur Bond Formation Using Na2S2O3as the Sulfur Source
inferredcites →https://doi.org/10.1039/c5cs00628gopenalex-snapshot
The medicinal chemist's toolbox for late stage functionalization of drug-like molecules
inferredcites →https://doi.org/10.1039/c6ob02833kopenalex-snapshot
Recent developments in sulfur–carbon bond formation reaction involving thiosulfates
inferredcites →https://doi.org/10.1039/c7qo00492copenalex-snapshot
Catalyst-free [3 + 2] cyclization of imines and Morita–Baylis–Hillman carbonates: a general route to tetrahydropyrrolo[2,1-a]isoquinolines and dihydropyrrolo[2,1-a]isoquinolines
inferredcites →https://doi.org/10.1039/c8cc04543gopenalex-snapshot
Convenient synthesis of selenyl-indoles via iodide ion-catalyzed electrochemical C–H selenation
inferredcites →https://doi.org/10.1039/c8nj06412aopenalex-snapshot
Metal-free, green and efficient oxidative α halogenation of enaminones by halo acid and DMSO
inferredcites →https://doi.org/10.1039/d1ob00005eopenalex-snapshot
Unprecedented access to functionalized pyrrolo[2,1- a ]isoquinolines from the domino reaction of isoquinolinium ylides and electrophilic benzannulated heterocycles
inferredcites →https://doi.org/10.1039/d2nj03164gopenalex-snapshot
Copper catalyzed reaction of alcohols, alkyl halides and Na 2 S 2 O 3 : an odorless and ligand-free route to unsymmetrical thioether synthesis
inferredcites →https://doi.org/10.1039/d2ob00209dopenalex-snapshot
Recent progress in the synthesis of pyrrolo[2,1- a ]isoquinolines
inferredcites →https://doi.org/10.1039/d4qo00396aopenalex-snapshot
Review of application of the I 2 and dimethyl sulfoxide combined reagent system to aryl methyl ketones for diverse transformations
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Successful treatment of calciphylaxis with intravenous sodium thiosulfate
inferredcites →https://doi.org/10.1055/a-1677-5971openalex-snapshot
Alkylation Reactions with Alkylsulfonium Salts
inferredcites →https://doi.org/10.1055/a-2508-2171openalex-snapshot
HI/DMSO-Based Chemoselective Oxidative Halogenation of Pyrrolo[2,1-a]isoquinolines
inferredcites →https://doi.org/10.1055/s-0035-1560429openalex-snapshot
Dimethyl Sulfoxide as a Synthon in Organic Chemistry
inferredcites →https://doi.org/10.3390/md13031105openalex-snapshot
Anticancer Properties of Lamellarins
inferredcites →https://doi.org/10.3390/molecules27238480openalex-snapshot
Recent Advances in DMSO-Based Direct Synthesis of Heterocycles
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