SYNTHESIS OF OLEFINS BY NICKEL-CATALYZED DECARBONYLATION OF S-(2-PYRIDYL) THIOATES
作者:Toshio Goto、Makoto Onaka、Teruaki Mukaiyama
DOI:10.1246/cl.1980.709
日期:1980.6.5
S-(2-Pyridyl) thioates, especially derived from secondary and tertiary carboxylicacids, are decarbonylated by use of a catalytic amount of nickel chloride and zinc powder to give olefins in good yields.
REDUCTIVE COUPLING OF<i>S</i>-(2-PYRIDYL) ALIPHATIC THIOATES BY USE OF BIS(1,5-CYCLOOCTADIENE)NICKEL
作者:Makoto Onaka、Yoshio Matsuoka、Teruaki Mukaiyama
DOI:10.1246/cl.1980.905
日期:1980.8.5
S-(2-Pyridyl) aliphatic thioates are reductively dimerized to give α-diketones and α-hydroxy ketones on treatment with bis(1,5-cyclooctadiene)nickel at 40°C.