Acetobromomaltose, a new source of carbohydrate radicals. EPR characterisation of maltosyl and 2-deoxymaltos-2-yl radicals and syntheses of tetrasaccharide-like mimics, maltal, 3-alpha-maltosyl propiononitrile, 1,5-anhydromaltitol and 2-deoxymaltopyranoside

The acetoxy-protected maltosyl radical 1, obtained through bromine abstract ion from acetobromomaltose (ABM), was studied by means of EPR spectroscopy. At room temperature, only the spectrum of 1 was observed, but at higher te mperatures a second radical, the acetoxy-protected 2-deoxymaltos-2-yl radic al 2, was detected, resulting from migration of an acetoxy group from posit ion 2 to position 1. Some acetoxy-protected maltose derivatives were prepar ed from ABM, via different radical pathways involving 1 and 2 as intermedia tes. Electroreduction on silver provides tetrasaccharide-like mimics 7 and maltal 8. Photochemical generation of 1, followed by trapping with tributyl tinhydride or with acrylonitrile, leads respectively to 1,5-anhydromaltitol 9 and to 3-alpha-maltosyl propiononitrile 10. Generation of 2 at 80 degree s C by 1-->2 isomerisation, followed by trapping with tributyltinhydride, l eads to 2-deoxymaltopyranoside 11. (C) 2000 Elsevier Science Ltd. All right s reserved.