82937-31-3Relevant academic research and scientific papers
ALUMINIUM-CHLORIDE CATALYZED REACTION OF ALLYLIC SULFIDES WITH METHYL PROPIOLATE: A NOVEL ADDITION REACTION VIA AN IONIC SIGMATROPIC REARRANGEMENT
Hayakawa, Kenji,Kamikawaji, Yoshimasa,Kanematsu, Ken
, p. 2171 - 2174 (1982)
The aluminium-chloride catalyzed reaction of allylic sulfides with methyl propiolate resulted in the clean formation of novel 1:1 adducts via ionic sigmatropic rearrangements.
Stereoselective Addition Reaction of Allylic Sulfides to Acetylenic Esters: E/Z Stereochemical Variations by Lewis Acid
Hayakawa, Kenji,Kamikawaji, Yoshimasa,Wakita, Akemi,Kanematsu, Ken
, p. 1985 - 1989 (2007/10/02)
The Lewis acid catalyzed addition reactions of allylic sulfides to methyl propiolate (MP) and dimethyl acetylenedicarboxylate (DMAD) have been investigated.The stereochemical outcome is considerably influenced by the Lewis acid.While the AlCl3-catalyzed r
