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Abstract
A unique and efficient 2,2,2-trifluoroethanol-activated one-pot reaction of β-nitroenamines, secondary amines and aromatic aldehydes was developed under mild and convenient conditions. In the presence of 2,2,2-trifluoroethanol (TFEA), aromatic aldehydes were activated by hydrogen bonding with TFEA. The newly-developed reaction could afford the desired Mannich-like products in moderate to excellent yields with wide substrate scopes.
Published Version
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