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Figure 1
(A) Synthesis of alkene synthon of 7-oxabicyclo[2.2.1]hept-5-ene core (1) and transformation of anhydride moiety into more stable 2,3-dicarboximide group (3). (B) Transformation of 3 to 4 using mCPBA oxidation, and its three-dimensional arrangement with conserved stereochemical control. |

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