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Direct Oxidative Heck Cyclizations: Intramolecular Fujiwara–Moritani Arylations for the Synthesis of Functionalized Benzofurans and Dihydrobenzofurans
233
Citations
44
References
2004
Year
Intramolecular Fujiwara–moritani ArylationsCross-coupling ReactionEngineeringExtra Functionalization StepBiochemistryHeterocyclicNatural SciencesFunctionalized BenzofuransDihydrobenzofuran DerivativesOrganic ChemistryCatalysisHeck CyclizationsChemistryHeterocycle ChemistryStereoselective SynthesisAsymmetric CatalysisSynthetic ChemistryBiomolecular Engineering
No extra functionalization step is required for palladium(II)-catalyzed oxidative carbocyclizations like that shown, which provide highly substituted benzofuran and dihydrobenzofuran derivatives by net dehydrogenation. The mechanism is similar to that of Heck cyclizations. Products containing quaternary carbon stereocenters can be obtained in diastereomerically pure form. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2004/z461294_s.pdf or from the author. 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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