A general strategy for diverse syntheses of anhydrolandomycinone, tetrangulol, and landomycinone?

Chemical Communications Pub Date: 2018-01-26 DOI: 10.1039/C7CC09818A

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.

Graphical abstract: A general strategy for diverse syntheses of anhydrolandomycinone, tetrangulol, and landomycinone
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