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Published on: June 8, 2016
Visible-light-mediated β,β-thio- and selenosulfonylation of N-ethyl tertiary amines
Pallaba Ganjan Dalai1, Dinabandhu Barik1, Supriya Manna1
1Department of Chemistry, Indian Institute of Technology Guwahati, 781039, Assam, India. patel@iitg.ac.in.
Abstract:
A visible-light-driven strategy for the geminal C(sp3)-H bis-functionalization of N-ethyl tertiary amines via both radical fragments, generated from organic thio/seleno sulfonates, has been accomplished. This protocol enables the synthesis of β,β-thio and selenosulfonylated enamines under metal and external oxidant-free conditions. The reaction proceeds via eosin Y-mediated activation of the amine and concurrent EDA complex formation between I- and thio/selenosulfonate.
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