Issue 6, 2011
From the journal:

Chemical Communications

Total synthesis of (±)-maistemonine and (±)-stemonamide†

Zhi-Hua Chen,a   Yong-Qiang Zhang,a   Zhi-Min Chen,a   Yong-Qiang Tu*a  and  Fu-Min Zhang*a  

* Corresponding authors

a State Key Laboratory of Applied Organic Chemistry & Department of Chemistry, Lanzhou University, Lanzhou 730000, P. R. China
E-mail: tuyq@lzu.edu.cn
Fax: +86 931-8915557

Abstract

The first total synthesis of polycyclic Stemonaalkaloid maistemonine has been achieved. The efficient approach features a stereoselective intramolecular Schmidt reaction, a ketone–ester condensation, and a Reformatsky reaction. Additionally, another Stemonaalkaloid stemonamide was divergently synthesized from a common intermediate.

Graphical abstract: Total synthesis of (±)-maistemonine and (±)-stemonamide

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C0CC02612C
Article type
Communication
Submitted
16 Jul 2010
Accepted
12 Nov 2010
First published
01 Dec 2010

Chem. Commun., 2011,47, 1836-1838

Permissions

Request permissions

Total synthesis of (±)-maistemonine and (±)-stemonamide

Z. Chen, Y. Zhang, Z. Chen, Y. Tu and F. Zhang, Chem. Commun., 2011, 47, 1836 DOI: 10.1039/C0CC02612C

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