Issue 17, 2018
From the journal:

Organic Chemistry Frontiers

Total synthesis of (±)-swermirin†

Ping Hea  and  Zhang Wang ORCID logo *a  

* Corresponding authors

a University at Albany, State University of New York, 1400 Washington Avenue, Albany NY, USA
E-mail: zwang9@albany.edu

Abstract

The total synthesis of the anti-HBV natural product (±)-swermirin is described. Key steps include two sequential regioselective Stille cross coupling reactions, selective oxidative cleavage and spontaneous 6π-electrocyclization.

Graphical abstract: Total synthesis of (±)-swermirin

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C8QO00655E
Article type
Research Article
Submitted
02 júl 2018
Accepted
25 júl 2018
First published
27 júl 2018

Org. Chem. Front., 2018,5, 2552-2554

Permissions

Request permissions

Total synthesis of (±)-swermirin

P. He and Z. Wang, Org. Chem. Front., 2018, 5, 2552 DOI: 10.1039/C8QO00655E

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