1988
DOI: 10.3987/com-87-4459
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One pot Synthesis of 3,4-Bis(methoxycarbonyl)-2-trimethylsilylfurans by Diels-Alder Reaction

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Cited by 6 publications
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“…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 …”
Section: Methodsmentioning
confidence: 99%
“…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 …”
Section: Methodsmentioning
confidence: 99%
“…[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.…”
Section: Mc~(ic~mentioning
confidence: 99%