Issue 11, 2011
From the journal:

Chemical Communications

A biomimetic approach to the cylindrospermopsin alkaloids†

Daniel M. Evansa  and  Patrick J. Murphy*a  

* Corresponding authors

a School of Chemistry, Bangor University, Bangor, Gwynedd, UK
E-mail: chs027@bangor.ac.uk
Fax: +44 (0)1248 370528
Tel: +44 (0)1248 382375

Abstract

The tethered Biginelli condensation between hemiaminal 21 and β-keto ester 22 is reported, leading to a model tricyclic core of the cylindrospermopsin alkaloids.

Graphical abstract: A biomimetic approach to the cylindrospermopsin alkaloids

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Article information

DOI
https://doi.org/10.1039/C0CC05034B
Article type
Communication
Submitted
18 Nov 2010
Accepted
07 Jan 2011
First published
24 Jan 2011

Chem. Commun., 2011,47, 3225-3226

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A biomimetic approach to the cylindrospermopsin alkaloids

D. M. Evans and P. J. Murphy, Chem. Commun., 2011, 47, 3225 DOI: 10.1039/C0CC05034B

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