K. Shishido et al., DIASTEREOSELECTIVE TOTAL SYNTHESES OF (-)-TRIPTOQUINONE-B AND TRIPTOQUINONE-C(), Journal of the Chemical Society, Chemical Communications, (9), 1993, pp. 793-794
The first and efficient total syntheses of (+/-)-triptoquinone B 1 and
C2 have been achieved from the allyl ether3; the key steps are the co
nstruction of the four contiguous stereogenic centres present in 2 by
the Mn(III) mediated oxidative free radical cyclisation followed by me
tal hydride reduction.