Publication | Closed Access
Synthesis and chemoselective ligations of MIDA acylboronates with O-Me hydroxylamines
73
Citations
43
References
2014
Year
Enantioselective SynthesisEngineeringBiochemistryNatural SciencesBioconjugationUnprotected Peptide SubstratesPeptide SynthesisOrganic ChemistryPeptide ScienceChemoselective Amide-bondChemistryNatural Product SynthesisSynthetic ChemistryBio-orthogonal ChemistryBiomolecular EngineeringChemoselective Ligations
A chemoselective amide-bond forming ligation of <italic>N</italic>-methyliminodiacetyl (MIDA) acylboronates and <italic>O</italic>-Me hydroxylamines, including unprotected peptide substrates, is described.
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