Metallaphotoredox Deoxygenative Arylation of Alcohols: A Viable Strategy for the Synthesis of Tryptamine Derivatives
Year: 2025
Type: article
Abstract: A metallaphotoredox deoxygenative arylation of alcohols strategy has been applied to prepare in a one pot procedure tryptamine derivatives. Starting from 3‐Br indoles and 2‐amino alcohols, in the presence of an Ir photocatalyst and catalytic amounts of NiBr 2 , 3‐(2‐aminoethyl)‐substituted indoles have been synthesized in up to 76% yield after 2 h under blue LED irradiation. Improved productivity and space time yield were observed when continuous flow technologies were employed (60% yield with 30 min residence time).
Source: ChemCatChem
Institution: University of Milan
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
Awards: G348699015, G8489333194, G972786147
OpenAlex ID: W4409234053
