Bader, S. L. and Kessler, S. N. and Zampese, J. A. and Wegner, H. A.. (2013) Exploration of 1,2-phenylenediboronic esters as potential bidentate catalysts for organic synthesis. Chemical monthly, Vol. 144, H. 4. pp. 531-537.
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Official URL: http://edoc.unibas.ch/dok/A6212085
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Abstract
Recently, we described the first inverse electron demand Diels–Alder reaction of 1,2-diazene catalyzed by a bidentate Lewis acid. Herein we investigate 1,2-phenylenediboronic esters as potential catalysts for this transformation offering higher stability and easier handling than the currently used boranthracene derivatives. Different 1,2-phenylenediboronic esters were prepared and their ability to form bidentate coordination complexes with phthalazine was analyzed. Although a 1:1 complex was observed, X-ray analysis revealed binding only in a monodentate fashion.
Faculties and Departments: | 05 Faculty of Science 05 Faculty of Science > Departement Chemie 05 Faculty of Science > Departement Chemie > Former Organization Units Chemistry > Organische Synthese (Wegner) |
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UniBasel Contributors: | Wegner, Hermann A. A. and Zampese, Jennifer Ann and Kessler, Simon and Bader, Samuel Lorenz and Bader, Samuel |
Item Type: | Article, refereed |
Article Subtype: | Research Article |
Publisher: | Springer |
ISSN: | 0026-9247 |
Note: | Publication type according to Uni Basel Research Database: Journal article |
Last Modified: | 31 Jan 2014 09:50 |
Deposited On: | 31 Jan 2014 09:50 |
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