Heck cyclization and trapping of the resultant η3-allylpalladium intermediate by a tethered diketopiperazine is the central step in a new stereocontrolled route to spirotryprostatin alkaloids. The versatility of this approach is illustrated by the enantioselective total syntheses of the fungal natural product (−)-spirotryprostatin B (1) and three stereoisomers.
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Overman et al. (2000) studied this question.
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