Examples of 'corresponding compounds' in a sentence
Meaning of "corresponding compounds"
corresponding compounds - Denotes chemical substances that are related or match one another in terms of their properties or structures, commonly used in chemistry or scientific contexts
How to use "corresponding compounds" in a sentence
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corresponding compounds
Corresponding compounds may be used by themselves or in a mixture.
Examples of actual procedures employed in the syntheses of the corresponding compounds are described below.
Corresponding compounds can be used on their own or in a mixture.
All of these salts may be prepared by conventional means from the corresponding compounds.
A wide variety of corresponding compounds may be obtained commercially.
Compounds of formula XXXIIc result from the hydrazinolysis of the corresponding compounds of type XXXIIb.
Corresponding compounds of the hydrogen isotopes differ slightly in their physical properties.
The exact conditions for the corresponding compounds can be found in the experimental part.
Corresponding compounds can be prepared by this procedure by substituting hydrobromic acid for hydrochloric acid.
The substituted aminoalcohols used as reactants are prepared according to literature procedures for corresponding compounds.
The corresponding compounds of formula LA may be prepared as described above.
These molecules possess distinctive pharmacological features from the corresponding compounds bearing a carboxylic acid group.
The corresponding compounds of formulae LA may then be prepared as described above.
In the Examples following abbreviations are used for the corresponding compounds.
Corresponding compounds of the formula V are obtained directly.
See also
corresponding components
corresponding compound
corresponding configuration
corresponding connection
corresponding compound
corresponding configuration
corresponding connection
Such compounds can also be formed from the corresponding compounds of the formula IVA.
Corresponding compounds in which G is S may be prepared from the corresponding thiophenolic starting materials.
Compounds of formula XXXIIIA may be prepared in analogous fashion to corresponding compounds of formula I.
The corresponding compounds of general formula ( II ) were obtained in high yield and purity.
Hydrogenation of the compounds having formula IX yields the corresponding compounds of the formula X.
Corresponding compounds can be used as intermediates for the manufacture of the compound of formula ( I ).
Here again, a wide variety of corresponding compounds are commercially available.
In addition, each of these methods leads only to the specific corresponding compounds.
Two deprotection steps then give the corresponding compounds according to general formula 1.
Protection of the N1-position with the triisopropylsilyl moiety afforded the corresponding compounds.
Converting compounds of formula ( I ) into corresponding compounds of formula ( l ) by employing suitable reaction techniques.
Scheme 2 illustrates the synthesis of compounds of formula I from the corresponding compounds of formula II.
Corresponding compounds wherein R2 represents C1 to 3 alkyl may be prepared using analogous methods.
Carbapenems and monobactams are likewise converted into corresponding compounds with an open B-lactam ring.
Normally, in corresponding compounds of formula ( II c ), wherein R2 is hydrogen, one would expect a racemisation.
Illustrative and representative species of the present invention include, and the corresponding compounds where X is S.
Compounds wherein R3 is alkyl can be prepared from the corresponding compounds wherein R3 is hydrogen.
They can be reacted with NH-containing cyclics 7 as nucleophiles to provide the corresponding compounds 8.
The phenol in thiourea can be protected with TBSCl to form the corresponding compounds 7-scheme 1.
Illustrative electrophiles represented by the formula Aryl - ( CH2 ) n-Z provide the corresponding compounds.
The residue was chromatographed yielding the corresponding compounds A4a and A4b.
Alkylation and deprotection as described in SCHEMES 1 and 2 affords the corresponding compounds of Formula I.
The residue was chromatographed yielding the corresponding compounds B4a and B4b.
Further branching of R1 or R2 reduces the potency of the corresponding compounds.
B4 when subjected to procedures described in Scheme 1 gives the corresponding compounds of Formula ( Ib ).
Second step, reduction of the compounds ( II ) into the corresponding compounds ( I ).
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