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The title compounds were prepared using benzotriazole as the synthon, through several synthetic steps.
The blended compounds were prepared using the standard water of consistency.
Several compounds were prepared using different polymer matrices and a broad range of carbon black types.
Target compounds were prepared using an enantioselective synthesis employing a highly specific enzyme-catalysed resolution of racemic n-butyl 4-benzylmorpholine-2-carboxylate (26) as the key step.
A number of compounds were prepared using this methodology and tested for their in vitro anti-proliferative properties against cancer (leukemia) and non-cancerous cell lines.
A series of bi-metallic oxygen reduction catalysts derived from pyrolyzed Fe M (where M = Co, Cu, Ni and Mn) and 4-aminoantipyrine (Fe M AAPyr) compounds were prepared using a sacrificial support method (SSM).
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The second set of phenothiazinium compounds was prepared using similar conditions and reacting 2- N-methylamino)ethanol to give 4-I, morpholin to yield 5-I or 4-N-methyl-piperazine to give 6-I, respectively, with moderate to good yields.
The pair of structurally related {FeIII4DyIII4} and {MnIII4LnIII4} saddle-compounds were prepared using distinct amine-triol and diols, respectively, indicating a robust topology, which though superficially similar to (13) and (14), are quite distinct.
The peak area of the compound was divided by that of the IS, and then a calibration curve for the compound was prepared using the peak area ratio and the known concentrations.
The ether-linked compounds 7– 9 were prepared using similar methods.
In an effort to find inhibitors that are effective against both Candida and Aspergillus spp., a series of 5 6 - un)substituted benzotriazole analogs, represented by compounds 3a–3h and 3b′–3f′, were prepared using a crystalline oxirane intermediate 1 previously synthesized in our laboratory.
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