Issue 13, 2015
From the journal:

Chemical Communications

Synthesis of spiroindanes by palladium-catalyzed oxidative annulation of non- or weakly activated 1,3-dienes involving C–H functionalization†

Imtiaz Khan,ab   Suresh Reddy Chidipudiab  and  Hon Wai Lam*ab  

* Corresponding authors

a EaStCHEM, School of Chemistry, University of Edinburgh, Joseph Black Building, The King's Buildings, West Mains Road, Edinburgh, UK

b School of Chemistry, University of Nottingham, University Park, Nottingham, UK
E-mail: hon.lam@nottingham.ac.uk
Tel: +44-115-748-4677

Abstract

The synthesis of spiroindanes by the palladium-catalyzed oxidative annulation of non- or weakly activated 1,3-dienes with 2-aryl cyclic 1,3-dicarbonyl compounds is described. Examples of the dearomatizing oxidative annulation of 1,3-dienes with 1-aryl-2-naphthols are also presented.

Graphical abstract: Synthesis of spiroindanes by palladium-catalyzed oxidative annulation of non- or weakly activated 1,3-dienes involving C–H functionalization

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Article information

DOI
https://doi.org/10.1039/C4CC09496D
Article type
Communication
Submitted
27 Nov 2014
Accepted
23 Dec 2014
First published
09 Jan 2015

Chem. Commun., 2015,51, 2613-2616

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Synthesis of spiroindanes by palladium-catalyzed oxidative annulation of non- or weakly activated 1,3-dienes involving C–H functionalization

I. Khan, S. R. Chidipudi and H. W. Lam, Chem. Commun., 2015, 51, 2613 DOI: 10.1039/C4CC09496D

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