Issue 8, 2015
From the journal:

Organic & Biomolecular Chemistry

A novel enantioselective synthesis of 6H-dibenzopyran derivatives by combined palladium/norbornene and cinchona alkaloid catalysis†

Di Xu,a   Li Dai,a   Marta Catellani,b   Elena Motti,b   Nicola Della Ca’b  and  Zhiming Zhou*a  

* Corresponding authors

a School of Chemical Engineering and the Environment, Beijing Institute of Technology, Beijing 100081, PR China
E-mail: zzm@bit.edu.cn
Tel: +86-10-68918982

b Dipartimento di Chimica and CIRCC, Università di Parma, Parco Area delle Scienze, 17/A, 43124 Parma, Italy

Abstract

Organometallic and organo-catalysts are cooperatively at work in the enantioselective synthesis of dibenzopyran derivatives; palladium/norbornene and a cinchona alkaloid base guarantee good yields and satisfactory enantioselectivities in a one-pot reaction.

Graphical abstract: A novel enantioselective synthesis of 6H-dibenzopyran derivatives by combined palladium/norbornene and cinchona alkaloid catalysis

About
Cited by
Related
Download options Please wait...

Associated articles

Supplementary files

Article information

DOI
https://doi.org/10.1039/C4OB02551B
Article type
Communication
Submitted
06 Dec 2014
Accepted
05 Jan 2015
First published
05 Jan 2015

Org. Biomol. Chem., 2015,13, 2260-2263

Author version available

Download author version (PDF)

Permissions

Request permissions

A novel enantioselective synthesis of 6H-dibenzopyran derivatives by combined palladium/norbornene and cinchona alkaloid catalysis

D. Xu, L. Dai, M. Catellani, E. Motti, N. Della Ca’ and Z. Zhou, Org. Biomol. Chem., 2015, 13, 2260 DOI: 10.1039/C4OB02551B

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