Cover Picture: Antiaromaticity to Aromaticity: From Boroles to 1, 2‐Azaborinines by Ring Expansion with Azides (Chem. Eur. J. 32/2014). Issue 32 (4th August 2014)

• Record Type: Journal Article
• Authors: Braunschweig, Holger; Hörl, Christian; Mailänder, Lisa; Radacki, Krzysztof; Wahler, Johannes
• Is Part Of: Chemistry. Volume 20:Issue 32(2014)
• Page Start: 9817
• Page End: 9817
• Publication Date: 2014-08-04
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/chem.201490132
• Languages: English
• ISSNs: 0947-6539

Abstract

<abstract abstract-type="graphical" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <bold>1, 2‐Azaborinines</bold> can be synthesized by a ring‐expansion reaction of boroles with azides. Such BN heterocycles are very interesting for applications in material science and biochemistry owing to their close resemblance to benzene. For more details on the synthesis and characterization of these molecules, see the Communication by H. Braunschweig et al. on <ext-link ext-link-type="doi" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">page 9858 ff.</ext-link><boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pghwhbv10s" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /></boxed-text></p> </abstract>