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Issue 37, 2008
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Direct functionalization at the boron center of antiaromatic chloroborole

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Abstract

The presence of a reactive B–Cl bond allowed for the direct functionalization of the boron center in antiaromatic chloroborole ClBC4Ph4, thus allowing for a selective fine tuning of the optical properties of borole derivatives and facilitating a potential new approach toward the introduction of borole moieties into the backbone of organic π-conjugated frameworks.

Graphical abstract: Direct functionalization at the boron center of antiaromatic chloroborole

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Supplementary files

Article information


Submitted
19 May 2008
Accepted
12 Jun 2008
First published
30 Jul 2008

Chem. Commun., 2008, 4487-4489
Article type
Communication

Direct functionalization at the boron center of antiaromatic chloroborole

H. Braunschweig and T. Kupfer, Chem. Commun., 2008, 4487
DOI: 10.1039/B808483A

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