SYNTHESIS OF IKARUGAMYCIN: MODEL STUDIES ON A NEW STRATEGY FOR THE CLOSURE OF RING C

Article abstract of DOI:10.1016/S0040-4039(00)89067-X

A new conjugated addition-alkylation approach suitable for the closure or ring C of ikarugamycin is demonstrated by the concise elaboration of a trans-disubstituted cyclopentane that has been converted into the cyclopentane analogue of the natural product