A general strategy for diverse syntheses of anhydrolandomycinone, tetrangulol, and landomycinone
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10.1039/c7cc09818a
Abstract
A general synthetic strategy based on a protecting group-promoted CH arylation method was developed for total syntheses of anhydro-landomycinone (1), tetrangulol (2), and landomycinone (3) from the same set of starting materials.