Examples of 'protected compound' in a sentence
Meaning of "protected compound"
protected compound - a secure area or facility that is safeguarded and restricted in access
How to use "protected compound" in a sentence
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protected compound
The protected compound is then phosphorylated as described above.
He said you went to the protected compound.
The protected compound may then be combined with a suitable base.
An acid addition salt is also an amino protected compound.
The resultant protected compound is then deprotected according to procedures known in the art.
The scope of the present invention encompasses all such protected compound forms and mixtures thereof.
The resultant protected compound may be deprotected according to procedures known in the art.
The residue is purified on silica gel chromatography to give Boc protected compound.
The protected compound of formula I is then phosphorylated as described above.
Reducing the compound of formula VII to form an optionally protected compound of formula VIII.
The obtained protected compound I must then be deprotected by standard methods.
Alternatively, such prodrugs can be prepared by reacting a suitably protected compound with a suitable progroup.
The protected compound ( IIa ) can be isolated by evaporation of the organic solvent.
A preferred sterile form of the protected compound of Formula ( LA ) is a lyophilised solid.
The protected compound is then reacted with diphosphorus pentasulphide in pyridine to obtain a 4-thio compound.
See also
This displacement reaction produces the optionally protected compound which has been depicted as I '.
The bis-alloc protected compound and unreacted starting material were recycled using the following procedure,.
The carboxylic acid is then decarboxylated using standard methods to provide the protected compound ( VI ).
The intermediate t-Boc protected compound was purified by column chromatography on a silica column.
Following acidification, coupling with an acid yields the protected compound 42.
Forming the protected compound of Formula 7 by reacting with bromomethylmethyl ether and diisopropylethylamine in dichloromethane ;.
Having a Lys residue, to give a protected compound of Formula LA.
A protected compound according to claim 16 where PROTECTING GROUP is benzyloxycarbonyl.
Steps 3 and 4 can be performed sequentially without isolation of the protected compound of formula ( d ).
When no protected compound remained ( ∼ 1 h ) the solvent was evaporated under reduced pressure.
After 20 min. the solvent was removed and the protected compound purified by silica gel chromatography.
The protected compound was obtained by 1 % TFA in dichloromethane cleavage.
The filtrates are concentrated under vacuum to give the Troc-amino protected compound 23.
Deprotecting a protected compound of formula ( II ), where Pg is an alcohol protecting group ;.
Reverse phase chromatographic purification of a protected compound of Formula ( LA ),.
By deprotecting a protected compound of formula II wherein " Pg " is a suitable alcohol protecting group ;.
Synthesis of benzyl protected Compound 1.
Forming the protected compound of Formula 26 by reacting with t-butyldiphenylsilyl chloride and dimethylaminopyridine in dichloromethane ;.
A -- For the preparation of a protected compound of formula II.
A protected compound according to claim 16 where PROTECTING GROUP is t - butoxycarbonyl.
Deprotecting a protected compound of formula ( I ).
The solvent of the fractions was evaporated under reduced pressure to give a protected compound ( 3.1 g ).
The use of ethanolamine to deprotect Protected Compound ( I ), in the presence of a solvent followed by.
The protected compound ( 2 ) can also be prepared by reacting compound ( 1 ) with a diazo compound in a solvent.
The use of ethanolamine to deprotect Protected Compound ( I ), followed by.
A protected compound according to claim 16 where RA is,.
Procedure G, Removal of the Boc-Protecting group The protected compound is stirred in 4N HCl / dioxane for 1 hour.
The Boc protected compound was treated with trifluoroacetic acid ( 6ml ) at room temperature for 30 minutes.
Standard work-up and purification afforded the protected compound in 93 % yield.
Formation of the protected compound of Formula 14 by reacting 2 with tert - butoxycarbonyl anhydride ;.
The reaction mixture was purified on reverse phase HPLC to give Boc protected compound ( 160mg ).
Here, pederic acid is added to the protected compound in LiHMDS and THF, producing a 75% yield.
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