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Strategy for <i>O</i>-Alkylation of Serine and Threonine from Serinyl and Threoninyl Acetic Acids by Photoinduced Decarboxylative Radical Reactions: Connection between Serine/Threonine and Carbohydrates/Amino Acids at the Side Chain
23
Citations
32
References
2018
Year
EngineeringSynthetic PhotochemistryOrganic ChemistryChemistryThreoninyl Acetic AcidsPhotoredox ProcessPhotocatalysisThreonine DerivativesBiochemistryPhotochemistryHydroxy GroupBiocatalysisMechanistic PhotochemistryRadical (Chemistry)CatalysisSide ChainBiomolecular EngineeringCarbohydrates/amino AcidsNatural SciencesEnzyme Catalysis
O-Alkylations of serine and threonine derivatives at the hydroxy group were achieved using photoinduced decarboxylative radical reactions of serinyl and threoninyl acetic acids with an organic photocatalyst without racemization under mild conditions. Photoinduced decarboxylative radical additions of serinyl and threoninyl acetic acids to electron-deficient alkenes provided linked serine and threonine with carbohydrates and amino acids at the side chain. In addition, O-methylations containing deuterium and O-benzylation of serine were performed under similar photochemical conditions.
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