Hari, Durga Prasad and Hering, Thea and Koenig, Burkhard (2014) The Photoredox-Catalyzed Meerwein Addition Reaction: Intermolecular Amino-Arylation of Alkenes. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 53 (3). pp. 725-728. ISSN 1433-7851, 1521-3773
Full text not available from this repository. (Request a copy)Abstract
A variety of amides are efficiently accessible under mild conditions by intermolecular amino-arylation using a photo Meerwein addition with visible light. The reaction has a broad substrate scope, tolerates a large range of functional groups, and was applied to the synthesis of a 3-aryl-3,4-dihydroisoquinoline.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | ARYL DIAZONIUM SALTS; C-H ARYLATION; ORGANIC-SYNTHESIS; METAL-FREE; LIGHT; RADICALS; PHOTOOXIDATION; GENERATION; COMPLEXES; CHEMISTRY; amino-arylation; aryl radicals; Meerwein addition; photocatalysis; visible light |
| Subjects: | 500 Science > 540 Chemistry & allied sciences |
| Divisions: | Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Burkhard König |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 28 Nov 2019 10:04 |
| Last Modified: | 28 Nov 2019 10:04 |
| URI: | https://pred.uni-regensburg.de/id/eprint/10817 |
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