Issue 9, 2014
From the journal:

Organic & Biomolecular Chemistry

Synthesis of benzannulated heterocycles by twofold Suzuki–Miyaura couplings of cyclic diarylborinic acids†

Elena Dimitrijević,a   Madeline Cusimanoa  and  Mark S. Taylor*a  

* Corresponding authors

a Department of Chemistry, University of Toronto, 80 St. George St., Toronto, ON M5S 3H6, Canada
E-mail: mtaylor@chem.utoronto.ca

Abstract

Two-fold Suzuki–Miyaura cross-couplings of cyclic diarylborinic acids are described. This novel annulation method enables the synthesis of benzo-fused heterocycles from dihaloarenes or gem-dibromoolefins.

Graphical abstract: Synthesis of benzannulated heterocycles by twofold Suzuki–Miyaura couplings of cyclic diarylborinic acids

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C3OB42065E
Article type
Communication
Submitted
15 Oct 2013
Accepted
19 Jan 2014
First published
28 Jan 2014

Org. Biomol. Chem., 2014,12, 1391-1394

Permissions

Request permissions

Synthesis of benzannulated heterocycles by twofold Suzuki–Miyaura couplings of cyclic diarylborinic acids

E. Dimitrijević, M. Cusimano and M. S. Taylor, Org. Biomol. Chem., 2014, 12, 1391 DOI: 10.1039/C3OB42065E

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