Journal
RSC ADVANCES
Volume 5, Issue 114, Pages 94328-94331Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ra18459b
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Funding
- Guangdong Natural Science Foundation [S2013010012465]
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With the activation of P(OEt)(3) and I-2, carboxylic acids can smoothly react with various primary and secondary amines, affording a series of amides, including peptides without racemization. P-31 NMR spectroscopy studies showed that carboxylic phosphoric mixed anhydride was the reactive intermediate and a possible mechanism was herein proposed.
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