Bulletin of the Chemical Society of Japan p. 2711 - 2715 (1980)
Update date:2022-08-05
Topics:
Kanai, Hiroyoshi
Kushi, Kenji
Sekanoue, Kei
Kishimoto, Nobuji
Selective cis-isomerization of 1-pentene was carried out by NiX(PPh3)3 (X = halogen and pseudohalogen).First-order plots were obtained except for the iodo-complex.The addition of tin(II) chloride increased both activities and ratios of cis-2-pentene to the trans-isomer.Protic solvents accelerated the isomerization.Isotopic exchange between C2D4 and C2H4 or 1-pentene reveals that a metal hydride addition-elimination mechanism is operative.
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