Chemistry Letters p. 1901 - 1904 (1983)
Update date:2022-07-29
Topics:
Fujisawa, Tamotsu
Itoh, Toshiyuki
Sato, Toshio
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.
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Doi:10.1007/BF00758835
(1984)Doi:10.1021/jo01069a528
(1961)Doi:10.1021/jo0525682
(2006)Doi:10.1016/S0040-4039(01)80019-8
(1984)Doi:10.1021/acs.joc.9b01280
(2019)Doi:10.1016/0022-328X(84)85144-X
(1984)
