Article ; Online: Decarboxylative Anti-Michael Addition to Olefins Mediated by Photoredox Catalysis.
Organic letters
2016 Volume 18, Issue 14, Page(s) 3494–3497
Abstract: ... access to anti-Michael-type products from readily available precursors. The scope of this methodology was ...
Abstract | Decarboxylative coupling of carboxylic acids with activated olefins has been accomplished using visible light photoredox catalysis. The strategic placement of a radical-stabilizing aromatic group at the β-position of the olefin component biases the regioselectivity of the addition, allowing reliable, facile access to anti-Michael-type products from readily available precursors. The scope of this methodology was demonstrated with a range of carboxylic acids and appropriately substituted olefins and was applied toward a two-step synthesis of the antiarrhythmic agent encainide. |
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Language | English |
Publishing date | 2016-07-15 |
Publishing country | United States |
Document type | Journal Article |
ISSN | 1523-7052 |
ISSN (online) | 1523-7052 |
DOI | 10.1021/acs.orglett.6b01712 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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