Cinchona alkaloid-based chiral catalysts act as highly efficient multifunctional organocatalysts for the asymmetric conjugate addition of malonates to nitroolefins?
Organic & Biomolecular Chemistry Pub Date: 2015-08-19 DOI: 10.1039/C5OB01351H
Abstract
New pentaerythritol tetrabromide-based chiral quaternary ammonium salts acting as organocatalysts (7a and 7b) have been prepared and used as organocatalysts for enantioselective Michael addition reactions between various nitroolefins and Michael donors (malonates) under mild reaction conditions, such as lower concentration of base and catalyst and room temperature, with very good chemical yields (up to 97%) and ee's (up to 99%).
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Journal Name：Organic & Biomolecular Chemistry
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CAS no.: 89640-58-4
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