90032-93-2Relevant articles and documents
THE HIGHLY SELECTIVE REACTION OF LITHIUM DITHIOESTER ENOLATES WITH β-ALKENYL-β-PROPIOLACTONES: A SIMPLE METHOD FOR THE SYNTHESIS OF 6-(METHYLTHIO)THIOCARBONYL-(E)-3-ALKENOIC ACIDS
Fujisawa, Tamotsu,Itoh, Toshiyuki,Sato, Toshio
, p. 1901 - 1904 (2007/10/02)
Lithium dithioester enolates were found to react with β-alkenyl-β-propiolactones highly regio- and stereoselectively at the terminal vinyl carbon to give 6-(methylthio)thiocarbonyl-(E)-3-alkenoic acids, masked 1,7-dicarboxylic compounds.