Abstract
A synthetic route to exo-2-phenyl-7-azabicyclo[2.2.1]heptane-1-carboxylic acid (a constrained proline analogue) in which the key step is the Diels-Alder reaction between (Z)-2-phenyl-4-benzylidene-5(4H)-oxazolone and Danishefsky's diene is described.
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