Examples of 'corresponding compound' in a sentence
Meaning of "corresponding compound"
corresponding compound - in chemistry, a compound that is related in structure and properties to another compound
How to use "corresponding compound" in a sentence
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corresponding compound
Cinacalcet can be prepared by coupling of an aryl halide with an appropriate corresponding compound.
References disclosing each corresponding compound are indicated in the parentheses after the names of compounds.
Cleavage of the protecting group provides the corresponding compound of formula IS.
To form the corresponding compound of formula XVI.
The resulting cyano derivative is then hydrolyzed to form the corresponding compound of formula IX.
Such is converted to the corresponding compound of formula VI as described above.
The resulting intermediate is then oxidized to convert it to the corresponding compound of Formula I.
A specific example of a corresponding compound is one satisfying the formula,.
Deprotection using methanolic ammonia or sodium methoxide in methanol yields the corresponding compound of formula 27.
This reaction yeilds the corresponding compound of formula XXXIV.
The corresponding compound of formula I-D can then be prepared as follows.
This directly yields the corresponding compound of the formula III.
Corresponding compound in Z-form compound No.
A two step process is then used to prepare the corresponding compound of the formula VIII.
Deprotecting a corresponding compound that comprises one or more protecting groups to provide the compound ; and.
See also
Which is hydrolysed to obtain the corresponding compound of formula I.
The protected corresponding compound of Formula 2 is isolated by conventional means ( such as evaporation ).
Hydrolysis of the compound of formula VIII yields the corresponding compound of formula IX.
To form the corresponding compound of formula ( III ).
Alkylation of the compound of formula XII yields the corresponding compound of formula XIII.
The corresponding compound of formula ( Ea ) is then crystallized from a suitable solvent, preferably isopropanol.
The four isomers of the corresponding compound I are thus obtained.
Lactonization may be achieved using p - toluenesulfonic acid monohydrate in toluene to give the corresponding compound 124.
Dissolving vecuroniumbromide or said corresponding compound in water saturated with carbondioxide or an organic solvent ;.
Suzuki coupling of the bicyclo-hetero compound 2 with suitable boronic acid 3 produces the corresponding compound 4.
Deprotection yields the corresponding compound of formula 28.
The compound ( III ) is reduced in a solvent to thereby give the corresponding compound ( IV ).
Comparatively, the corresponding compound comprising a maleimide moiety was 70 % degraded after one hour in PBS.
This reaction directly leads to corresponding compound I.
The corresponding compound wherein R20 is methyl is pyrrolysine.
Wherein A has the above definition to obtain the corresponding compound of formula I.
To form the corresponding compound of formula ( I ).
Deprotection of a compound of formula ( III ) produces the corresponding compound of formula ( II ).
Reaction of a corresponding compound of formula ( IIa ), wherein,.
Oxidation followed by saponification gives the corresponding compound of Structure 31.
To form the corresponding compound of formula ( Va ) ;.
Removal of the protecting groups P from a compound of formula 25 provides the corresponding compound of formula 23.
Reaction of a corresponding compound of formula ( II ),.
The compound of formula ( IV ) is in turn converted into a corresponding compound of formula ( V ).
The corresponding compound of formula ( I ) is produced ;.
The numbers in brackets represent the corresponding compound in Table 1.
The alkene group of compound 2-5 can be reduced by hydrogenation to afford the corresponding compound 2-6.
Treating a piperidone having formula II, with a corresponding compound of formula R1Li in an aprotic solvent ;.
Compounds of Formula 6, Compounds of Formula 6 can be prepared by reducing a corresponding compound of Formula 7.
The number given the corresponding compound in Table 1 . IC 50.
Trituration or column chromatography ( methanol / ethyl acetate ) gave the corresponding compound of Formula I.
When R2 is methyl, methylation of the corresponding compound of formula ( I ) wherein R2 is hydrogen ; or.
Reaction of HCOCH3 with a peracid, followed by hydrolysis gives the corresponding compound wherein R7 is hydroxy.
Catalytic hydrogenolysis to yield the corresponding compound of formula ( XLVI ).
The compound of formula ( IX ) is de-protected to yield the corresponding compound of formula ( II ).
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