“…1 H and 13 C spectra were recorded on a 400 MHz spectrometer. Starting alkenes were prepared according to the following known literature procedures: 1a , 1b , 1c , 1d , 1e , 1f , 1h , 1i , 1j , and 1k …”
The ruthenium catalyzed dimerization of oxanorbornadiene dicarboxylates was studied. The effects of the ester moiety and the addition of a C1 substituent to the bicyclic alkene on the reaction were explored, and moderate yields and excellent regioselectivities were obtained.
“…1 H and 13 C spectra were recorded on a 400 MHz spectrometer. Starting alkenes were prepared according to the following known literature procedures: 1a , 1b , 1c , 1d , 1e , 1f , 1h , 1i , 1j , and 1k …”
The ruthenium catalyzed dimerization of oxanorbornadiene dicarboxylates was studied. The effects of the ester moiety and the addition of a C1 substituent to the bicyclic alkene on the reaction were explored, and moderate yields and excellent regioselectivities were obtained.
“…[n benzene or xylene their reaction leads to a bicyclic adduct, which decomposes when heated to 200°C into acetylene and 2-trimethylsilyl-3,4-bis(methoxycarbonyl)furans [310]. If the reaction is conducted with heat and without the solvent, it is not possible to detect the bicyclic adduct on account of its rapid decomposition [410]. The catalytic hydrogenation of trimethyl(2-furyl)silane and a series of furylgermanes over Raney nickel and platinum and palladium black in the liquid phase and over Pd/C in the gas phase was investigated.…”
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