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Asymmetric One‐Pot Four‐Component Coupling Reaction: Synthesis of Substituted Tetrahydropyrans Catalyzed by Diphenylprolinol Silyl Ether
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2011
Year
EngineeringOrganic ChemistryChemistryJournalismDiphenylprolinol Silyl EtherInformationLanguage StudiesContent AnalysisCross-coupling ReactionElectronic PublishingSubstituted TetrahydropyransDer TitelprozessDetailed FactsCatalysisInformation ManagementSiehe SchemaAsymmetric CatalysisEnantioselective SynthesisScholarly CommunicationSynthetic Chemistry
Dominoeffekt: Der Titelprozess führt über asymmetrische Michael/Henry-Reaktion, Acetalisierung und Lewis-Säure-vermittelte Allylierung mit ausgezeichneter Enantioselektivität zu hoch substituierten Tetrahydropyranen (siehe Schema; TMS=Trimethylsilyl). Alle Kohlenstoffatome im Tetrahydropyranring tragen unterschiedliche Substituenten, und die relative und absolute Konfiguration der fünf benachbarten Kohlenstoffzentren ist genau vorgegeben. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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