Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/66008
Title: Transition metal-free iminoiodane-mediated amination of activated C-H bonds
Authors: Tejo, Ciputra
Keywords: DRNTU::Science::Chemistry::Organic chemistry
Issue Date: 2016
Source: Tejo, C. (2016). Transition metal-free iminoiodane-mediated amination of activated C-H bonds. Doctoral thesis, Nanyang Technological University, Singapore.
Abstract: Novel transition metal-free-mediated amination of C–H bonds with the use of arylsulfonyliminophenyliodinane (PhI=NSO2Ar) have been developed. The use of iodine(III) compound has shown to be compatible under Brønsted acid and base conditions for the synthesis of unnatural amino ester derivatives and aziridines from 1,3-dicarbonyl compounds, respectively. The amination of cyclic ethers with iminoiodanes was explored subsequently. These cyclic ethers could undergo ring opening and further functionalization with nucleophiles was realized to give the 2-substituted cyclic ether and amino alcohol products under their respective reaction conditions.
URI: https://hdl.handle.net/10356/66008
DOI: 10.32657/10356/66008
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Theses

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