58431-65-5Relevant academic research and scientific papers
STEREOSPECIFIC SYNTHESIS OF ALKENYL SULPHIDES BY CROSS-COUPLING REACTIONS OF SECONDARY ALKYL GRIGNARD REAGENTS WITH Z- OR E-1-BROMO-2-PHENYLTHIOETHENE IN THE PRESENCE OF TRANSITION METAL CATALYSTS
Fiandanese, Vito,Miccoli, Giovanni,Naso, Francesco,Ronzini, Ludovico
, p. 343 - 348 (1986)
Z- and E-1-bromo-2-phenylthioethenes were cross-coupled stereospecifically with s-alkyl Grignard reagents in the presence of a series of NiII, PdII, or FeIII catalysts with the aim of finding a catalyst which would not cau
Homologation of aldehydes using (phenylthiomethylene) triphenylarsorane: Selective preparation of α-thiophenoxyepoxides and phenylthioenol ethers
Boubia,Mioskowski,Manna,Falck
, p. 6023 - 6026 (2007/10/02)
The title arsonium ylide reacts with aldehydes to give exclusively α-thiophenoxyepoxides in THF and phenylthioenol ethers in THF/HMPA. The former adducts are readily transformed to α-thiophenoxy carbonyls and the latter to one-carbon homologated aldehydes.
