in chloroform-d1 slight excess of cyclooctadiene was added to a CDCl3 coln. of Pt-complex, reaction was followed by (1)H NMR until equil. was reached; products were identified by their (1)H NMR spectra;
in chloroform-d1 slight excess of the diolefine was added to a CDCl3 coln. of Pt-complex, reaction was followed by (1)H NMR until equil. was reached; products were identified by their (1)H NMR spectra;
in chloroform-d1 slight excess of the diolefine was added to a CDCl3 coln. of Pt-complex, reaction was followed by (1)H NMR until equil. was reached; products were identified by their (1)H NMR spectra;
in chloroform-d1 slight excess of the diolefine was added to a CDCl3 coln. of Pt-complex, reaction was followed by (1)H NMR until equil. was reached; products were identified by their (1)H NMR spectra;
in ethanol; water in a microwave oven (Fischer-Porter reaction vessel) at 140°C for 0.5 min; elem. anal.;
参考文献
Baghurst, David R.; Mingos, D. Michael P.
Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1992 , # 7 p. 1151 - 1156
