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Furanosylidene and Iminofuranosylidene Complexes: Synthesis by Stoichiometric Olefin Metathesis and Ring-Opening/Mitsunobu-Recyclization Sequence
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1999
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Ring-opening/mitsunobu-recyclization SequenceCross-coupling ReactionNovel OrganocatalystsEngineeringAlkene MetathesisCoordination ComplexOrganic ChemistryOrganometallic CatalysisTransition MetalChemistryAsymmetric CatalysisNovel Organometallic GlycoconjugatesBiomolecular EngineeringIminofuranosylidene ComplexesStoichiometric Olefin Metathesis
Transition metal activated furanosylidenes and iminofuranosylidenes are accessible by stoichiometric olefin metathesis and a ring-opening aminolysis/Mitsunobu recyclization sequence. The methodology has been applied to the synthesis of novel organometallic glycoconjugates (see picture).