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1  rate of H2 release at the late stage of 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 id-mediated C-C triple bond cleavage and the dehydrogenation reaction.
5 n oxidized product in a cobaloxime-catalyzed dehydrogenation reaction.
6 rsors supported on Al(2)O(3) for the propane dehydrogenation reaction.
7 al data indicate ligand participation in the dehydrogenation reaction.
8  for the industrially important light alkane dehydrogenation reaction.
9 t via in situ one-pot metal/ligand oxidative-dehydrogenation reactions.
10 dox neutral deamination versus the oxidative dehydrogenation reactions.
11 us materials that are proficient in enabling dehydrogenation reactions.
12 transition metal catalyzed hydrogenation and dehydrogenation reactions.
13 present in CO/CO(2) hydrogenation and alkane dehydrogenation reactions.
14 electivity for both VA synthesis and ethanol dehydrogenation reactions.
15  to formic acid and methanol and the reverse dehydrogenation reactions.
16 il but typically only catalyze desaturation (dehydrogenation) reactions.
17 red for practical yields in such endothermic dehydrogenation reactions (700-900 K).
18  affect the rate of electron transfer in the dehydrogenation reactions, and are likely transmitted fr
19 tions, we show that the active sites for the dehydrogenation reaction are copper(I) cations hosted in
20 ossible mechanisms for the thermally induced dehydrogenation reaction are discussed.
21                                              Dehydrogenation reactions are key steps in many metal-ca
22 (DFT) study of the mechanism of the methanol dehydrogenation reaction catalyzed by [RuH(2)(H(2))(PPh(
23                                          The dehydrogenation reaction catalyzed by human glutaryl-CoA
24 he two-electron oxidation (hydroxylation and dehydrogenation) reactions catalyzed by its more extensi
25 CD) is unique: in addition to the alpha,beta-dehydrogenation reaction, common to all ACDs, GCD cataly
26 tized in a final step through a DDQ-mediated dehydrogenation reaction (DDQ=2,3-dichloro-5,6-dicyano-1
27 g of alkenes to copper(I) sites promotes the dehydrogenation reaction, enabling the yield of alkene m
28 ion step; a mutant (D361T) that retained the dehydrogenation reaction exhibited the same deuterium is
29 l transitions by dissociative adsorption and dehydrogenation reactions involving chlorine and carboxy
30                                          The dehydrogenation reaction is compatible with molecular ox
31 mplex 3, the active catalytic species in the dehydrogenation reaction, is independently synthesized a
32               Subsequent chain-branching and dehydrogenation reactions lead ultimately to a cross-lin
33  a sealed evacuated tube at 100 degrees C, a dehydrogenation reaction occurs to form a new rhenium co
34 ein, we report a Pd(II)-catalyzed sequential dehydrogenation reaction of free aliphatic acids via bet
35 ion of TiH(2) on the equilibrium pressure of dehydrogenation reaction of MgH(2).
36 rface intermediates in situ during catalytic dehydrogenation reactions of high-pressure cyclohexane (
37  H-MFI and on the monomolecular cracking and dehydrogenation reactions of n-butane.
38 understand various oxidative electrochemical dehydrogenation reactions on oxide and hydroxide-based c
39 istic and structural characteristics of this dehydrogenation reaction, positioning NdasCDO as a promi
40           Experimental data suggest that the dehydrogenation reaction proceeds over the other two rea
41 .05 and 1.01 +/- 0.05 in the deamination and dehydrogenation reactions, respectively, using Na(2)S(2)
42 iation of an o-QM intermediate in a benzylic dehydrogenation reaction that links the newly described
43 idine-pyridone ligands that enable divergent dehydrogenation reactions through palladium-catalyzed B-
44 nter and an unprecedented vinylogous Saegusa dehydrogenation reaction to address C-ring functionality
45                    Coupled with an oxidative dehydrogenation reaction to crack acetylene at reduced t
46 arrying out non-oxidative and CO(2)-mediated dehydrogenation reactions to ensure unambiguous comparis
47 xample of a homogeneous and selective alkane dehydrogenation reaction using a base-metal titanium cat
48 tionally flexible polymer chains followed by dehydrogenation reactions using thermal annealing.
49       By contrast, HppE catalyses an unusual dehydrogenation reaction while converting the secondary