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In the presence of 2-amino-2-phenylpropanoate salt (2a or 2e) as the amine source, aromatic aldehydes underwent decarboxylative transamination under very mild conditions to produce a variety of arylmethylamines in 44-99%… Click to show full abstract
In the presence of 2-amino-2-phenylpropanoate salt (2a or 2e) as the amine source, aromatic aldehydes underwent decarboxylative transamination under very mild conditions to produce a variety of arylmethylamines in 44-99% yields. The work has provided an efficient new method for the synthesis of primary arylmethylamines.
Keywords:
aldehydes primary;
transamination aromatic;
primary arylmethylamines;
aromatic aldehydes
Journal Title: Organic letters
Year Published: 2023
Link to full text (if available)
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Journal Title: Organic letters
Year Published: 2023
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!