Issue 12, 2012
From the journal:

Organic & Biomolecular Chemistry

Efficient syntheses of 2,3-disubstituted natural quinazolinones via iridium catalysis†

Jie Fanga  and  Jianguang Zhou*a  

* Corresponding authors

a Chemical and Analytical Development, Suzhou Novartis Pharma Technology Co. Ltd, Changshu, Jiangsu, China
E-mail: jianguang.zhou@novartis.com

Abstract

Natural products sclerotigenin, pegamine, deoxyvasicinone, mackinazolinone, and rutaecarpine were synthesized. Core quinazolinone structures were constructed via Ir catalysis.

Graphical abstract: Efficient syntheses of 2,3-disubstituted natural quinazolinones via iridium catalysis

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Article information

DOI
https://doi.org/10.1039/C2OB07178A
Article type
Communication
Submitted
26 Dec 2011
Accepted
23 Jan 2012
First published
25 Jan 2012

Org. Biomol. Chem., 2012,10, 2389-2391

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Efficient syntheses of 2,3-disubstituted natural quinazolinones via iridium catalysis

J. Fang and J. Zhou, Org. Biomol. Chem., 2012, 10, 2389 DOI: 10.1039/C2OB07178A

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