%0 Journal Article %A Abdelli, Abderrahmen %A M'rabet, Hedi %A Lotfi Efrit, Mohamed %A Gaucher, Anne %A Prim, Damien %D 2014 %T γ-Alkylsulfide phosphonates through the thia-Michael strategy %U https://tandf.figshare.com/articles/journal_contribution/_947_Alkylsulfide_phosphonates_through_the_thia_Michael_strategy/1157575 %R 10.6084/m9.figshare.1157575.v2 %2 https://tandf.figshare.com/ndownloader/files/1657249 %K strategy %K alkylsulfide %K phosphonate moiety %K esters groups %X

The formation of γ-alkylsulfide phosphonates is described from allylphosphonates under mild conditions using thiols through the thia-Michael strategy. A series of new phosphonates, bisphosphonates were cleanly prepared in high yields. The methodology developed allowed further preparing γ-alkylsulfide phosphonates bearing valuable esters groups in β and δ positions with respect to the phosphonate moiety.

%I Taylor & Francis