Diastereoselective Rhodium‐Catalyzed [(3+2+2)] Carbocyclization Reactions with Tethered Alkynylidenecyclopropanes: Synthesis of the Tremulane Sesquiterpene Natural Products

다국어 초록 (Multilingual Abstract)

The development of a diastereoselective intramolecular rhodium‐catalyzed [(3+2+2)] carbocyclization reactions of allyl ester‐tethered alkynylidenecyclopropanes (ACPs) for the construction of the 5,7,5‐tricyclic scaffold of the tremulane sesquiterpene natural products is described. This work illustrates that the stereoelectronic nature of the phosphite ligand is critical for attaining high levels of stereocontrol, which is supported by density functional theory (DFT) studies that indicate the migratory insertion step favors the formation of the cis‐diastereoisomer. Consequently, several strategies were devised to access the thermodynamically more stable trans‐diastereoisomer for the synthesis of the tremulanes; however, the attempts to either switch the sense of stereocontrol in the carbocyclization reaction or epimerize the C7 stereocenter of the cycloadduct provided only modest improvements. Hence, we elected to highlight the synthetic utility of this strategy with the development of concise and highly efficient syntheses of (±)‐epi‐tremulenolide A, (±)‐epi‐tremulenediol A and (±)‐epi‐ceriponol D.
A highly diastereoselective rhodium catalyzed [(3+2+2)] carbocyclization reaction is developed. In addition to experimental results, DFT studies also delineate the important role of the ligand in attaining excellent efficiency and selectivity. This protocol provides a direct approach to prepare 5,7,5‐tricyclic scaffold and useful compounds such as (±)‐tremulenolide A, (±)‐epi‐tremulenolide A, (±)‐epi‐tremulenediol A and (±)‐epi‐ceriponol D.