Issue 57, 2013
From the journal:

Chemical Communications

Biomimetic total syntheses of spirobacillenes A and B†

Hongzhi Yang,‡a   Juan Feng‡a  and  Yefeng Tang*a  

* Corresponding authors

a The Comprehensive AIDS Research Center, Department of Pharmacology & Pharmaceutical Sciences, School of Medicine, Tsinghua University, Beijing 100084, China
E-mail: yefengtang@tsinghua.edu.cn
Fax: +86 10 62797732
Tel: +86 10 62798236

Abstract

The first total syntheses of spirobacillenes A and B were achieved concisely. The key transformation leading to spirobacillene A features a biomimetic intramolecular phenol–enol oxidative coupling reaction, and that leading to spirobacillene B highlights a bio-inspired intramolecular indole–ketone enolate oxidative coupling reaction.

Graphical abstract: Biomimetic total syntheses of spirobacillenes A and B

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C3CC42686F
Article type
Communication
Submitted
12 Apr 2013
Accepted
29 May 2013
First published
30 May 2013

Chem. Commun., 2013,49, 6442-6444

Permissions

Request permissions

Biomimetic total syntheses of spirobacillenes A and B

H. Yang, J. Feng and Y. Tang, Chem. Commun., 2013, 49, 6442 DOI: 10.1039/C3CC42686F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements