A general strategy for diverse syntheses of anhydrolandomycinone, tetrangulol, and landomycinone†
Cheng-Jhe Sie,Venukumar Patteti,Yi-Ru Yang,Kwok-Kong Tony Mong
Chemical Communications Pub Date : 01/26/2018 00:00:00 , 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.
