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Peer-reviewedCC BY-NCRSC Advances

Oxidative functionalization of aliphatic and aromatic amino acid derivatives with H 2 O 2 catalyzed by a nonheme imine based iron complex

  • Barbara Ticconi
  • Arianna Colcerasa
  • Stefano Di Stefano
  • Osvaldo Lanzalunga
  • Andrea Lapi
  • Marco Mazzonna
  • Giorgio Olivo
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Abstract

-AcPheOMe. A marked preference for the aromatic ring hydroxylation over Cα-H and benzylic C-H oxidation was observed, leading to the clean formation of tyrosine and its phenolic isomers.

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Cite

BibTeXRIS
BibTeX
@article{ticconi2026oxidative,
  title = {{Oxidative functionalization of aliphatic and aromatic amino acid derivatives with H 2 O 2 catalyzed by a nonheme imine based iron complex}},
  author = {Barbara Ticconi and Arianna Colcerasa and Stefano Di Stefano and Osvaldo Lanzalunga and Andrea Lapi and Marco Mazzonna and Giorgio Olivo},
  journal = {RSC Advances},
  year = {2026},
  month = oct,
  doi = {10.1039/c8ra02879f},
  url = {https://hal.science/hal-05786853v1},
  note = {CC BY-NC},
}
RIS
TY  - JOUR
TI  - Oxidative functionalization of aliphatic and aromatic amino acid derivatives with H 2 O 2 catalyzed by a nonheme imine based iron complex
AU  - Barbara Ticconi
AU  - Arianna Colcerasa
AU  - Stefano Di Stefano
AU  - Osvaldo Lanzalunga
AU  - Andrea Lapi
AU  - Marco Mazzonna
AU  - Giorgio Olivo
PY  - 2026
DA  - 2026/10/08
JO  - RSC Advances
DO  - 10.1039/c8ra02879f
UR  - https://hal.science/hal-05786853v1
AB  - -AcPheOMe. A marked preference for the aromatic ring hydroxylation over Cα-H and benzylic C-H oxidation was observed, leading to the clean formation of tyrosine and its phenolic isomers.
SN  - 2046-2069
ER  -