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Since the quinone produced can further react non-enzymatically with other nucleophiles, e.g. amino groups, many tyrosinases have a recorded cross-linking activity on proteins.
In the presence of surface OH species, methyl formate can further react to form formic acid, which can finally dehydrogenate to produce CO2.
A number of reaction processes undergo yield drops since an intermediate target species can further react with one of the reactants generating lower volatility by-products.
These compounds can further react with BF3·Et2O to form novel dyes containing BODIPY (difluoroboradiazaindacene) analogue unit, by which both the absorption and emission maximum have been red-shifted further.
In the fine chemical and pharma industry a number of reaction processes undergo selectivity losses since the target product (typically a low volatility compound) can further react with one of the reactants leading to by-products that must be separated from the target product itself and finally disposed as wastes.
Copper chlorides and sulphates can further react to form other salts [127].
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These NO2 molecules can then further react with the excess NO (for example, from a NO donor drug) to form the potent nitrosating agent N2O3 facilitating further toxicity [ 37].
The oligoesters obtained from PET glycolysis can be further reacted with aliphatic diacids to form polyester polyols, which can be utilized as the starting material for polyurethane synthesis (Nikles and Farahat 2005).
The aldehyde can be further reacted with other materials to enhance properties.
Numerous side-products were observed during the process, but most of these can be further reacted or oxidised to form methylene linkages, and only minor amounts remain after heating to 205°C.
As in the gold reaction, the formation of 3a occurs at room temperature within the mixing time and can be further reacted with 2 equivalents of base in acetone, affording the final [Cu(Cl)(IPr)] complex (Scheme 3).
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