4.8 Article

Synthesis of cyclobutane lignans via an organic single electron oxidant-electron relay system

Journal

CHEMICAL SCIENCE
Volume 4, Issue 6, Pages 2625-2629

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3sc50643f

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Funding

  1. University of North Carolina at Chapel Hill
  2. NIGMS [R01 GM098340]
  3. Eli Lilly New Faculty Award

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A direct method to synthesize lignan cyclobutanes and analogs via photoinduced electron transfer is presented. A variety of oxygenated alkenes are employed to furnish terminal or substituted cyclobutane adducts with complete regiocontrol, yielding cycloadducts with trans stereochemistry. Key to minimizing competing cycloreversion is the inclusion of an aromatic electron relay (ER). This method has been adapted to the synthesis of the natural products magnosalin and pellucidin A.

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