Issue 15, 2018
From the journal:

Chemical Communications

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

Cheng-Jhe Sie,‡a   Venukumar Patteti,‡a   Yi-Ru Yanga  and  Kwok-Kong Tony Mong ORCID logo *a  

* Corresponding authors

a Department of Applied Chemistry, National Chiao Tung University, 1001, University Road, Hsinchu City, Taiwan, Republic of China
E-mail: tmong@mail.nctu.edu.tw

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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Article information

DOI
https://doi.org/10.1039/C7CC09818A
Article type
Communication
Submitted
26 Dec 2017
Accepted
25 Jan 2018
First published
26 Jan 2018

Chem. Commun., 2018,54, 1885-1888

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

C. Sie, V. Patteti, Y. Yang and K. T. Mong, Chem. Commun., 2018, 54, 1885 DOI: 10.1039/C7CC09818A

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