Abstract
A general synthetic strategy based on a protecting group-promoted CH arylation method was developed for total syntheses of anhydrolandomycinone (1), tetrangulol (2), and landomycinone (3) from the same set of starting materials.
| Original language | English |
|---|---|
| Pages (from-to) | 1885-1888 |
| Number of pages | 4 |
| Journal | Chemical Communications |
| Volume | 54 |
| Issue number | 15 |
| DOIs | |
| State | Published - 2018 |
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