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https://doi.org/10.1021/ol300280s
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Cite Journal: Organic Letters |  Publication Date: Feb 28, 2012 |
 Citations: 43 |
Affiliation: Kanazawa University
A synthetic study of actinophyllic acid based on an original strategy has been described. A transannular acyl radical cyclization allowed us to obtain a key bicyclo[3.3.2] framework, and construction of a core of the target alkaloid has been accomplished by subsequent introduction of a C2 unit.
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