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Tandem reactions via Barton Esters with intermolecular addition and vinyl radical substitution onto indole

Coyle, Robert
; 
McArdle, Patrick
; 
Aldabbagh, Fawaz
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Identifiers
http://hdl.handle.net/10379/5693
 https://doi.org/10.13025/14945
Publication Date
2014-05-16
Keywords
Chemistry, Cyclization, Generation, Route, Rings, Acids
Type
Article
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Robert Coyle, Patrick McArdle, Fawaz Aldabbagh (2014) 'Tandem Reactions via Barton Esters with Intermolecular Addition and Vinyl Radical Substitution onto Indole'. Journal Of Organic Chemistry, 79 :5903-5907.
Abstract
A one-pot initiator-free Barton ester decomposition with tandem radical addition onto alkyl propiolates or phenylacetylene with aromatic substitution of the resultant vinyl radical allows convenient access to new 9-substituted 6,7-dihydropyrido[1,2-a]indoles. Propyl radical cyclizations compete when forming the expanded 7,8-dihydro-6H-azepino[1,2-a]indole system. 2-Thiopyridinyl S-radical is incorporated into aromatic adducts when using unsubstituted indole-1-alkanoic acid precursors. X-ray crystallography on substitution products allows selectivity of the radical addition onto less reactive internal alkynes to be determined.
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Publisher
American Chemical Society
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Attribution-NonCommercial-NoDerivs 3.0 Ireland
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School of Biological and Chemical Sciences (Scholarly Articles)