摘要
The stereoselective synthesis of substituted [2,2,1]-bicyclo- heptan-2-one 12,a supposed intermediate to the spiroketal fragment of azadi- rachtin was described.When 12 was treated with mCPBA in CH_2Cl_2 in the pres- ence of excess amount of solid sodium bicarbonate,only 13 was obtained.The spiroketal intermediate 20 was converted from 9 through 5 steps by an alterna- tive route.
The stereoselective synthesis of substituted [2,2,1]-bicyclo- heptan-2-one 12,a supposed intermediate to the spiroketal fragment of azadi- rachtin was described.When 12 was treated with mCPBA in CH_2Cl_2 in the pres- ence of excess amount of solid sodium bicarbonate,only 13 was obtained.The spiroketal intermediate 20 was converted from 9 through 5 steps by an alterna- tive route.