Abdelli, Abderrahmen M'rabet, Hedi Lotfi Efrit, Mohamed Gaucher, Anne Prim, Damien γ-Alkylsulfide phosphonates through the thia-Michael strategy <div><p>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.</p></div> strategy;alkylsulfide;phosphonate moiety;esters groups 2014-09-12
    https://tandf.figshare.com/articles/journal_contribution/_947_Alkylsulfide_phosphonates_through_the_thia_Michael_strategy/1157575
10.6084/m9.figshare.1157575.v2