Abstract
The usefulness of flavin-based aerial photooxidation in esterification under Mitsunobu reaction conditions was demonstrated, providing aerial dialkyl azodicarboxylate recycling/generation from the corresponding dialkyl hydrazine dicarboxylate. Simultaneously, activation of triphenylphosphine (Ph3P) by photoinduced electron transfer from flavin allows azo-reagent-free esterification. An optimized system with 3-methylriboflavin tetraacetate (10%), oxygen (terminal oxidant), visible light (450 nm), Ph3P, and dialkyl hydrazine dicarboxylate (10%) has been shown to provide efficient and stereoselective coupling of various alcohols and acids to esters with retention of configuration.
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CITATION STYLE
März, M., Chudoba, J., Kohout, M., & Cibulka, R. (2017). Photocatalytic esterification under Mitsunobu reaction conditions mediated by flavin and visible light. Organic and Biomolecular Chemistry, 15(9), 1970–1975. https://doi.org/10.1039/c6ob02770a
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