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Merck

Photocatalytic Three-Component Umpolung Synthesis of 1,3-Diamines.

Organic letters (2018-10-24)
Thomas Rossolini, Jamie A Leitch, Rachel Grainger, Darren J Dixon
RESUMEN

A visible-light-mediated photocatalytic umpolung synthesis of 1,3-diamines from in situ-generated imines and dehydroalanine derivatives is described. Pivoting on a key nucleophilic addition of photocatalytically generated α-amino radicals to electron-deficient alkenes, this three-component coupling reaction affords 1,3-diamines efficiently and diastereoselectively. The mild protocol tolerates a wide variety of functionalities including heterocycles, pinacol boronates, and aliphatic chains. Application to biologically relevant α-amino-γ-lactam synthesis and extension to 1,3-aminoalcohols is also demonstrated.

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Sigma-Aldrich
2-(2,4-Difluorophenyl)-5-(trifluoromethyl)pyridine, ≥95%