1460271-98-0Relevant academic research and scientific papers
A direct synthetic route to allyl sulfides from cyclic Morita–Baylis–Hillman alcohols
Oueslati, Yosra,Abidi, Ahlem,Sbihi, Hassen Mohamed,Rezgui, Farhat
, p. 142 - 151 (2017/03/07)
p-TsOH-mediated the direct α-substitution of cyclic Morita–Baylis–Hillman alcohols with aliphatic and aromatic thiols in refluxing THF. The reaction proceeded with complete α-regioselectivity and provided the corresponding allyl sulfides in moderate to good yields.
A Metal-Free Synthesis of 2-Alkyl(or Aryl) Thiomethyl-2-cyclohexenones from Cyclic Morita–Baylis–Hillman Bromides
Baioui, Narjes,Abidi, Ahlem,Rezgui, Farhat
, p. 704 - 709 (2016/09/20)
Under mild conditions, an efficient and rapid S-allylation of thiols with cyclic Morita–Baylis–Hillman (MBH) bromides without the need of a transition-metal catalyst or an expensive additive is described herein. Treatment of the MBH bromides with various
Regioselective S -allylation of thiols with cyclic Baylis-Hillman acetates
Erray, Imen,Oble, Julie,Poli, Giovanni,Rezgui, Farhat
, p. 128 - 136 (2014/01/23)
An efficient and mild S-allylation of thiols with cyclic Baylis-Hillman acetates with no need of a transition-metal-catalyst or an expensive additive is described. Allyl sulfides are prepared in good to excellent yields (60-97%) and a single regioisomer was observed in all cases.
