Examples of 'resulting compounds' in a sentence
Meaning of "resulting compounds"
resulting compounds: substances that are formed or created as a result of a chemical reaction or process
How to use "resulting compounds" in a sentence
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resulting compounds
The resulting compounds are optionally dried and rechromatographed.
The precise structure of the resulting compounds is not known.
The resulting compounds have low water solubilities.
The physical properties of the resulting compounds are shown below.
The resulting compounds are then derivatized in three different ways.
The invention also relates to the resulting compounds as members of this class.
The resulting compounds are thio derivatives of the claimed compounds.
The successful functionalization was assessed by NMR and mass spectrometry analysis of the resulting compounds.
The resulting compounds are useful starting compounds in the synthesis of corticosteroids.
Again, chromatography is used to purify the resulting compounds.
The resulting compounds contain a carbonyl adjacent to the ring nitrogen of piperazine.
The spectral data etc . of the resulting compounds are shown below.
The resulting compounds are especially suitable synthetic materials due to their hardness.
Table 5 provides purity data and other data for the resulting compounds.
The resulting compounds are purified by flash column chromatography or silica gel chromatography.
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However, our studies indicate that the resulting compounds are less toxic than the fumonisins themselves.
The resulting compounds will have a low cost price which is very advantageous.
The physical properties of the resulting compounds are presented in Table 8.
The resulting compounds may be used as surfactants in accordance with the present invention.
The physical properties of the resulting compounds are shown in Table 9.
The resulting compounds can then evaporate from the surface and join the molecular cloud.
The freezing points of the resulting compounds are shown in Table 3.
The resulting compounds may be hydrogenated in a known manner to give further compounds of formula I.
Illustrative examples of substituted amines and the resulting compounds are shown in Table 1.
In all cases the resulting compounds are non volatile and therefore essentially odorless.
The physical properties of the resulting compounds are shown in Tables 1 to 4.
The resulting compounds are extracted into ethyl acetate and the compounds are purified by HPLC.
The physical properties of the resulting compounds are shown in Tables 5 and 6.
The resulting compounds showed outstanding MFI increases.
These studies indicate that the resulting compounds are less toxic than the fumonisins themselves.
The resulting compounds are referred to as Fc fusions of TMP tandem dimers.
The structure of the resulting compounds may be confirmed by NMR analysis.
The resulting compounds of Formula I may be isolated and purified by standard techniques.
Additionally, the resulting compounds are obtained in high purity.
The resulting compounds are converted to compounds of Formula I according to the foregoing chemistry.
The utility of the resulting compounds for nucleic acid photoreaction has not previously been reported.
The resulting compounds are designated by the expression “ alkylcyclohexanol alkoxylates ”.
If necessary, the resulting compounds may be purified by silica gel chromatography.
The resulting compounds are designated by the expression “ alkyl cyclohexanol alkoxylates ”.
If desired, the resulting compounds can be protected for use in peptide synthesis.
The resulting compounds demonstrate outstanding flow properties when compared to the unmodified polyamide 6.
In this case, the resulting compounds are of formula I where R2 is amino.
The resulting compounds are useful intermediates in the synthesis of therapeutically important steroids, particularly corticosteroids.
Accordingly, the resulting compounds of the invention are having a diastereomeric excess of at least 80 %.
The resulting compounds would, for example, then be converted into the respective stannane derivative.
If desired, the resulting compounds ( I ) can be converted to salts by a known process.
The resulting compounds are shown by the general Formula 6.
Method C, step 4, the resulting compounds of step 3 were converted into the corresponding derivatives.
The resulting compounds of Formula 54 can be convened into further homologs and derivatives.
The resulting compounds ( I ) can be formed into salts of the present invention in a usual manner.
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This guarantee excludes damage resulting from
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