Issue 1, 2011
From the journal:

Chemical Communications

Pushing the limits of steric demand around a biaryl axis: synthesis of tetra-ortho-substituted biaryl naphthalenes†‡

Adam C. Glass,a   Sam Klonoski,a   Lev N. Zakharov§a  and  Shih-Yuan Liu*a  

* Corresponding authors

a Department of Chemistry, University of Oregon, Eugene, Oregon 97403, USA
E-mail: lsy@uoregon.edu
Fax: +1 (541) 346-0487
Tel: +1 (541) 346-5573

Abstract

The synthesis of tetra-ortho-substituted biaryl naphthalenes, including examples bearing multiple ortho-isopropyl groups, has been developed via a catalytic rearrangement process.

Graphical abstract: Pushing the limits of steric demand around a biaryl axis: synthesis of tetra-ortho-substituted biaryl naphthalenes

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C0CC02170A
Article type
Communication
Submitted
29 Jun 2010
Accepted
27 Jul 2010
First published
23 Aug 2010

Chem. Commun., 2011,47, 286-288

Permissions

Request permissions

Pushing the limits of steric demand around a biaryl axis: synthesis of tetra-ortho-substituted biaryl naphthalenes

A. C. Glass, S. Klonoski, L. N. Zakharov and S. Liu, Chem. Commun., 2011, 47, 286 DOI: 10.1039/C0CC02170A

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