Journal
ORGANIC LETTERS
Volume 13, Issue 2, Pages 196-199Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol1023954
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Funding
- University of Minnesota through the Vince and McKnight Endowed Chairs
- ACS-Division of Medicinal Chemistry
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A highly convergent strategy to prepare phenanthroindolizidines is reported involving three consecutive C-C coupling reactions. This sequence features a novel VOF3-mediated aryl-alkene coupling in the final step, which enables regioselective preparation of C5-substituted phenanthroindolizidines for the first time. This strategy has been applied to the synthesis of eight natural and unnatural members in this class to investigate the scope of this chemistry and to explore structure-activity relationships.
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