Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction


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Article
Language
English
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Abstract
Glycal amides were prepared for the first time by reacting 2-iodo-D-glycals with L-amino acid esters via a Pd-catalyzed carbonylative cross-coupling reaction, by using Mo(CO)6 as the carbon monoxide source. Glycal amides were synthesized in moderate to good yields under our optimized conditions. In addition, the acetyl groups of the glucal amides could be readily removed to obtain the corresponding trihydroxy derivatives in good yields.
Reference
Jesus JC., Noguchi HK., Toledo MF.Z.J., Burrow RA., Pimenta DC, Stefani HA.. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction. European J Org Chem. 2022 Aug; 2022(30):e202200332. doi:10.1002/ejoc.202200332.
Link to cite this reference
https://repositorio.butantan.gov.br/handle/butantan/4473
URL
https://doi.org/10.1002/ejoc.202200332
Issue Date
2022


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