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A new route to 24-nortriterpene derivatives with 2-hydroxy-Delta(1,4)-cyclohexadien-3-one A-rings from triterpene precursors has been demonstrated beginning with betulin to prepare derivatives of betulinic acid. The key steps in the transformation are a Suárez cleavage of the A-ring with a subsequent SmI(2)-mediated pinacol-type coupling to reclose the A-ring following removal of the C-24 carbon by oxidative cleavage.
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Yonghong Deng
Tetraphase Pharmaceuticals (United States)
John K. Snyder
Boston University
The Journal of Organic Chemistry
Boston University
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Deng et al. (Thu,) studied this question.
synapsesocial.com/papers/6a2816b845b3314bfb2c7349 — DOI: https://doi.org/10.1021/jo010929h