Issue 36, 2016

Enantioselective bromocyclization of 2-geranylphenols induced by chiral phosphite–urea bifunctional catalysts

Abstract

Chiral phosphite–urea bifunctional catalysts have been developed for the enantioselective bromocyclization of 2-geranylphenols with N-bromophthalimide (NBP) for the first time. The chiral triaryl phosphite moiety activates NBP to generate a bromophosphonium ion. On the other hand, the urea moiety interacts with a hydroxyl group of the substrate through hydrogen bonding interactions. Enantioselectivity is effectively induced through two-point attractive interactions between the catalyst and the substrate.

Graphical abstract: Enantioselective bromocyclization of 2-geranylphenols induced by chiral phosphite–urea bifunctional catalysts

Supplementary files

Article information

Article type
Communication
Submitted
10 Jan 2016
Accepted
18 Mar 2016
First published
18 Mar 2016
This article is Open Access
Creative Commons BY license

Chem. Commun., 2016,52, 6068-6071

Enantioselective bromocyclization of 2-geranylphenols induced by chiral phosphite–urea bifunctional catalysts

Y. Sawamura, Y. Ogura, H. Nakatsuji, A. Sakakura and K. Ishihara, Chem. Commun., 2016, 52, 6068 DOI: 10.1039/C6CC00229C

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