Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4563
Title: The Barton radical decarboxylation on solid phase. A versatile synthesis of peptides containing modified amino acids
Authors: M. E., Attardi
Taddei, Maurizio 
Issue Date: 2001
Project: None 
Journal: TETRAHEDRON LETTERS
Abstract: 
Barton esters were prepared starting from different carboxylic acids loaded on a Wang resin. Light induced fragmentation occurred giving a radical that reacted with CBrCl3 to give the corresponding bromides, whereas conjugate addition to electron-poor alkenes proved to be less synthetically useful. The bromides so formed were further functionalised on the resin with different nucleophiles. (C) 2001 Elsevier Science Ltd. All rights reserved.
Description: 
45994
URI: http://hdl.handle.net/20.500.12779/4563
ISSN: 0040-4039
DOI: 10.1016/S0040-4039(01)00496-8
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