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The pyruvate so formed can then react via either step [50] or [50a].
Although both inner and loop primers react via the loops, they do so by different mechanisms.
These comonomers react via free radical copolymerization to yield void-free thermosets.
As reactions involving radicals typically react via the radical, it is assumed that these mappings are incorrect.
In the simulations fuel and oxidant react via a one-step, isothermal reaction (activation energy is set to zero).
In contrast when both react via catalytic trans-hydrogenation the yield of the olefin is increased without the need of hydrogen or separation technology.
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These two polymers reacted via Schiff-base reaction to form hydrozone linkages as cross-linking sites.
Pentachloroethane (PCA) reacted via concurrent reductive β-elimination (93%) and hydrolysis (7%).
At higher temperatures, therefore, larger, better-developed crystals reacted via an oriented aggregation mechanism, requiring a larger degree of order.
The interesting point here is the peculiar reaction of the FeF2 LiF composite which, although similar in composition to the electrochemically formed LiFeF3, reacts via a different pathway.
Esterification of the oligomer end groups with methacryloyl chloride led to divinyl terminated macromers that were reacted via photoinitiated polymerizations to produce crosslinked networks.
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