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https://doi.org/10.1002/anie.200503467
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Cite Publication Date: Jan 23, 2006 | |
 Citations: 28 |
Affiliation: Brandeis University
Three rings: Treatment of an N-2,2,2-trichloroethoxycarbonyl (Troc)-substituted tetrahydropyridinol (1) with BF3⋅Et2O in CH2Cl2 gave a tricyclic adduct 2 (31 % yield) through an intramolecular Diels–Alder reaction. Reduction with zinc gave deoxysymbioimine (3), a potential antiresorptive and anti-inflammatory drug.
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