Publication | Closed Access
Synthesis of Highly Functionalized Bicyclo[<i>m</i>.<i>n</i>.1]alkanones via a Cationic Reaction Cascade
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Citations
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References
2005
Year
Chemical EngineeringAcid-mediated Prins/pinacolEngineeringCross-coupling ReactionHeterocyclicDiversity Oriented SynthesisNatural SciencesDiversity-oriented SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisCationic Reaction CascadeChemistrySingle StepBiomolecular EngineeringHigh Molecular Complexity
[reaction: see text] The acid-mediated Prins/pinacol and the triple domino reactions Diels-Alder/Prins/pinacol were used to construct highly functionalized bicyclo[m.n.1]alkanones 19-29 and 33a-c possessing various ring sizes from ketals 8-18 and 31a-c in 44-96% yields. This approach proves to be highly efficient and reliable to generate high molecular complexity in a single step.
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