Search results for "C−H activation"

showing 3 items of 3 documents

1,2‐Benzothiazine Derivatives from Sulfonimidamides by Metal‐Catalyzed Annulation Reactions in Solution and under Solvent‐Free Mechanochemical Condit…

2021

Advanced synthesis & catalysis (2021). doi:10.1002/adsc.202001505 special issue: "Hot Topic: C-H Activation"

Annulationkemiallinen synteesiSolvent free660iridium catalysisChemistrysulfonimidamideGeneral ChemistryBenzothiazine12-benzothiazineC−H activationCatalysisMetalchemistry.chemical_compoundMechanochemistryvisual_artkatalyysirikkiyhdisteetddc:660visual_art.visual_art_mediumrhodium catalysisOrganic chemistrymechanochemistryorgaaniset yhdisteet
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Metal- and Reagent-Free Electrochemical Synthesis of Alkyl Arylsulfonates in a Multi-Component Reaction.

2020

Abstract This work presents the first electrochemical preparation of alkyl arylsulfonates by direct anodic oxidation of electron‐rich arenes. The reaction mechanism features a multi‐component reaction consisting of electron‐rich arenes, an alcohol of choice and excess SO2 in an acetonitrile‐HFIP reaction mixture. In‐situ formed monoalkyl sulfites are considered as key intermediates with bifunctional purpose. Firstly, this species functions as nucleophile and secondly, excellent conductivity is provided. Several primary and secondary alcohols and electron‐rich arenes are implemented in this reaction to form the alkyl arylsulfonates in yields up to 73 % with exquisite selectivity. Boron‐doped…

Reaction mechanismoxidationAlcohol010402 general chemistry01 natural sciencesCatalysisC−H activationchemistry.chemical_compoundradical ionsNucleophileMulti-component reactionElectrochemistryBifunctionalAlkylchemistry.chemical_classification010405 organic chemistrygreen chemistryCommunicationOrganic ChemistryGeneral ChemistryCombinatorial chemistryCommunications0104 chemical scienceschemistryReagentSelectivityChemistry (Weinheim an der Bergstrasse, Germany)
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Mo-Based Oxidizers as Powerful Tools for the Synthesis of Thia- and Selenaheterocycles.

2019

A highly efficient synthetic protocol for the synthesis of thia- and selenaheterocycles has been developed. By employing a MoCl5 -mediated intramolecular dehydrogenative coupling reaction, a broad variety of structural motifs was isolated in yields up to 94 %. The electrophilic key transformation is tolerated by several labile moieties like halides and tertiary alkyl groups. Due to the use of disulfide or diselenide precursors, a high atom efficiency was achieved.

chemistry.chemical_classificationcyclization010405 organic chemistryChemistryoxidationOrganic ChemistryHalideGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisCoupling reactionC−H activationsulfur heterocycles0104 chemical sciencesDiselenidemolybdenumAtom economyIntramolecular forceElectrophileStructural motifAlkylChemistry (Weinheim an der Bergstrasse, Germany)
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