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Synthesis of Cyclic 1-Alkenylboronates via Zr-Mediated Double Functionalization of Alkynylboronates and Sequential Ru-Catalyzed Ring-Closing Olefin Metathesis
20
Citations
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References
2013
Year
Zr-mediated Double FunctionalizationCross-coupling ReactionEngineeringHeterocyclicAlkene MetathesisNatural SciencesDiversity-oriented SynthesisNovel Cyclic 1-AlkenylboronatesOrganic ChemistryOrganometallic CatalysisCatalysisChemistryCyclic 1-AlkenylboronatesTriphenylene DerivativesBiomolecular Engineering
Synthesis of novel cyclic 1-alkenylboronates is accomplished through the zirconium-mediated regio- and stereoselective double functionalization of 1-alkynylboronates and the subsequent ruthenium-catalyzed ring-closing metathesis (RCM). The obtained substituted cyclic 1-alkenylboronates are transformed into o-terphenyl and triphenylene derivatives.
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