66164-74-7Relevant academic research and scientific papers
The effects of C-S and C-Se bonds on torquoselectivity: stereoselective olefination of α-thio and α-selenoketones with ynolates
Yoshikawa, Takashi,Mori, Seiji,Shindo, Mitsuru
experimental part, p. 8832 - 8838 (2010/04/06)
Highly Z-selective olefination of acyclic α-thio and α-selenoketones with ynolates has been achieved, and the theoretical calculations of the transition states in the ring-opening of the intermediates, the β-lactone enolates, revealed that the torquoselectivity was controlled by the secondary orbital interactions between the σ orbital of the C-S bond or a lone pair orbital on the S and σ* orbitals of the breaking C-O bond, and the σ orbital of the breaking C-O bond or a lone pair orbital on the O on the ring and the σ* orbitals of the C-S bond. The synthetic applications of the resulting olefins are also shown.
Scope and limitations of allyl sulphide synthesis by [1,2] and [1,3] phenylthio migration
Brownbridge, Peter,Warren, Stuart
, p. 2272 - 2285 (2007/10/05)
β-Phenylthio-alcohols rearrange in acidic solution (toluene-p-sulphonic acid in benzene under reflux) to give allyl sulphides by phenylthio migration. High yields of single products useful in organic synthesis are obtained with a tertiary or secondary mig
