142048-19-9Relevant articles and documents
Synthesis and diastereoselective complexation of enantiopure sulfinyl dienes: The preparation of sulfinyl iron(0) dienes
Paley, Robert S.,De Dios, Alfonso,Estroff, Lara A.,Lafontaine, Jennifer A.,Montero, Carlos,McCulley, David J.,Rubio, M. Belen,Ventura, Maria Paz,Weers, Heather L.,De la Pradilla, Roberto Fernandez,Castro, Sonia,Dorado, Rocio,Morente, Miguel
, p. 6326 - 6343 (2007/10/03)
The preparation of a diverse array of enantiomerically pure 1- and 2- sulfinyl dienes has been achieved via Stille coupling of halovinyl sulfoxides and vinyl stannanes, hydrogenation of 1-sulfinyl-1-en-3-ynes, or vinylcupration of 1-sulfinyl alkynes. Form
An easy synthesis of chiral sulfinyl allylic bromides and their use in the preparation of (R)(S)- and (S)(S)-2-p-tolylsulfinyl-1,3-alkadienes
Bonfand,Gosselin,Maignan
, p. 1667 - 1676 (2007/10/02)
Condensation of (R)-vinyl-o-tolylsulfoxide anion on carbonyl compounds led directly to chiral allylic sulfinylalcohols 1. By treatment with NBS/Me2S, these alcohols 1 were converted into the rearranged primary allylic bromides 2 via SN2/s