gsrp_a_951856_sm1977.docx (1.96 MB)
γ-Alkylsulfide phosphonates through the thia-Michael strategy
Version 2 2014-09-12, 07:36
Version 1 2014-09-12, 07:36
journal contribution
posted on 2014-09-12, 07:36 authored by Abderrahmen Abdelli, Hedi M'rabet, Mohamed Lotfi Efrit, Anne Gaucher, Damien PrimThe 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.