107977-90-2Relevant articles and documents
STEREOSELECTIVE SYNTHESIS OF POLYOLS PRECURSORS BY ALLYL SULPHINYL ANION ADDITION TO CHIRAL ALKOXY ALDEHYDES
Annunziata, Rita,Cinquini, Mauro,Cozzi, Franco,Raimondi, Laura,Stefanelli, Stefania
, p. 5451 - 5456 (1986)
Tandem condensation of chiral α-alkoxy and α,β-dialkoxy aldehydes with allylic sulphinyl anion, and thiophile promoted desulphurization of the resulting α-substituted allylic sulphoxide afford (E)-5-alkoxy-(or 5,6-dialkoxy)-2-alkene-1,4-diols, advanced polyols precursors, the major stereochemical path occuring via a Felkin-Ahn (non chelation control) mode.