53254-60-7Relevant articles and documents
SYNTHESES A L'AIDE DE SULFONES. XXIII. SUR LA SELECTIVITE DE LA SYNTHESE DES DULFONES ALLYLIQUES
Julia, Marc,Nel, Maurice,Righini, Anne,Uguen, Daniel
, p. 113 - 120 (1982)
The role of the palladium ligands on the yield and regioselectivity of the reaction of conjugated dienes with arenesulphinic acids (or of allylic acetates with sodium arenesulphinates) has been investigated.Arenesulphinic acids catalyse the isomerisation of allylic sulphones.
Synthesis of SHIP1-activating analogs of the sponge meroterpenoid pelorol
Meimetis, Labros G.,Nodwell, Matt,Yang, Lu,Wang, Xiaoxia,Patrick, Brian O.,Andersen, Raymond J.,Wu, Joyce,Harwig, Curtis,Stenton, Grant R.,MacKenzie, Lloyd F.,MacRury, Thomas,Ming-Lum, Andrew,Ong, Christopher J.,Mui, Alice L. -F.,Krystal, Gerald
, p. 5195 - 5207,13 (2020/08/31)
Two biomimetic approaches have been used to synthesize analogs of the SHIP1-activating sponge meroterpenoid pelorol (1). One approach started from the chiral pool plant natural product sclareolide, which has the same absolute configuration as pelorol. The
Asymmetric Induction Reactions. III. Palladium-Catalyzed Asymmetric Sulfonylations of Allylic Sulfinates and Acetates with Chiral Phosphine Ligands
Hiroi, Kunio,Makino, Kunitaka
, p. 1744 - 1749 (2007/10/02)
Treatment of allylic (+/-)-p-toluenesulfinate with tetrakis(triphenlphosphine)palladium in the presence of chiral phosphine ligands resulted in allylic sulfinate-sulfone rearrangements to give the corresponding optically active allylic sulfones in high op