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1 al data indicate ligand participation in the dehydrogenation reaction.
2 a catalyst resting state during the alcohol dehydrogenation reaction.
3 et radical chemistry is coopted to perform a dehydrogenation reaction.
4 for the industrially important light alkane dehydrogenation reaction.
5 rate of H2 release at the late stage of the dehydrogenation reaction.
6 t via in situ one-pot metal/ligand oxidative-dehydrogenation reactions.
7 dox neutral deamination versus the oxidative dehydrogenation reactions.
8 to formic acid and methanol and the reverse dehydrogenation reactions.
9 il but typically only catalyze desaturation (dehydrogenation) reactions.
10 affect the rate of electron transfer in the dehydrogenation reactions, and are likely transmitted fr
12 (DFT) study of the mechanism of the methanol dehydrogenation reaction catalyzed by [RuH(2)(H(2))(PPh(
14 he two-electron oxidation (hydroxylation and dehydrogenation) reactions catalyzed by its more extensi
15 CD) is unique: in addition to the alpha,beta-dehydrogenation reaction, common to all ACDs, GCD cataly
16 tized in a final step through a DDQ-mediated dehydrogenation reaction (DDQ=2,3-dichloro-5,6-dicyano-1
17 ion step; a mutant (D361T) that retained the dehydrogenation reaction exhibited the same deuterium is
18 mplex 3, the active catalytic species in the dehydrogenation reaction, is independently synthesized a
20 a sealed evacuated tube at 100 degrees C, a dehydrogenation reaction occurs to form a new rhenium co
22 rface intermediates in situ during catalytic dehydrogenation reactions of high-pressure cyclohexane (
24 .05 and 1.01 +/- 0.05 in the deamination and dehydrogenation reactions, respectively, using Na(2)S(2)
25 nter and an unprecedented vinylogous Saegusa dehydrogenation reaction to address C-ring functionality
26 xample of a homogeneous and selective alkane dehydrogenation reaction using a base-metal titanium cat
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