Examples of 'cyanoborohydride' in a sentence
Meaning of "cyanoborohydride"
Cyanoborohydride (noun) - A chemical compound used in organic synthesis, specifically for the reduction of various functional groups like aldehydes and ketones
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- The anion BH₃-C≡N⁻; any salt containing this anion
How to use "cyanoborohydride" in a sentence
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cyanoborohydride
As reducing reagent sodium cyanoborohydride can be used.
Sodium cyanoborohydride is disclosed as a useful reducing agent.
As reducing agent sodium cyanoborohydride may be used.
Sodium cyanoborohydride is the preferred alkali metal cyanoborohydride.
The reducing agent may be sodium cyanoborohydride.
Add sodium cyanoborohydride at ambient temperature.
The latter is reduced with sodium cyanoborohydride.
Sodium cyanoborohydride was used in the working examples below.
Most preferred as a reducing agent is sodium cyanoborohydride.
The use of sodium cyanoborohydride is preferred.
A particularly preferred reducing agent is sodium cyanoborohydride.
Acetic acid and sodium cyanoborohydride are then added.
A particularly suitable reducing agent is sodium cyanoborohydride.
Preferred reducing agents are sodium cyanoborohydride or sodium triacetoxyborohydride.
It would also be desirable to avoid the use of cyanoborohydride.
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G of sodium cyanoborohydride are cautiously added.
The preferred reducing agent is sodium cyanoborohydride.
Sodium cyanoborohydride are added.
A reducing agent such as sodium cyanoborohydride can be used.
Modification of gelonine by the simultaneous action of sodium periodate and sodium cyanoborohydride.
A reducing agent such as sodium cyanoborohydride may be used.
Examples of suitable reducing agents include sodium triacetoxy borohydride or sodium cyanoborohydride.
A subsequent reduction step with sodium cyanoborohydride is done at neutral pH.
Suitable reducing agents include sodium triacetoxyborohydride and sodium cyanoborohydride.
Other useful reducing agents are sodium cyanoborohydride and sodium borohydride.
The reducing agent used in the reductive alkylation of an amine was sodium cyanoborohydride.
Preferred hydride reducing agents include sodium cyanoborohydride or sodium triacetoxyborohydride.
Suitable reductive alkylating agents include sodium borohydride and sodium cyanoborohydride.
Cells incubated with biotinylated saponin without cyanoborohydride are used to provide a background measure.
The reduction is accomplished by treatment with sodium cyanoborohydride.
Sodium cyanoborohydride are added and the mixture is kept stirring for over night.
Other suitable reducing agents include sodium cyanoborohydride.
Subsequent reduction with sodium cyanoborohydride was performed in order to produce stable secondary amine linkages.
The resulting solution was treated with sodium cyanoborohydride.
A reducing agent such as sodium cyanoborohydride is added in small portions and reaction mixture stirred.
Ammonium acetate was added and then sodium cyanoborohydride.
The periodate is mixed with the cyanoborohydride before the addition of the GPIR.
Using sodium triacetoxyborohydride or sodium cyanoborohydride.
Using sodium cyanoborohydride or catalytically e . g.
This was accomplished by reductive amination using sodium cyanoborohydride.
Periodate oxidation and reduction by sodium cyanoborohydride of A chain blocked on the thiol group.
The reaction is conveniently performed using sodium cyanoborohydride.
Of these agents, sodium cyanoborohydride and sodium triacetoxyborohydride are preferred.
Typical reducing agents include borohydrides such as sodium cyanoborohydride.
This is reacted with butyraldehyde and sodium cyanoborohydride according to the method of Borch J.
A preferred reducing agent for this reaction is sodium cyanoborohydride.
G of sodium cyanoborohydride is then added in portions over 30 minutes at room temperature.
Typical reducing agents include sodium cyanoborohydride or triethylsilane.
Preferred metal hydride reducing agents include lithium aluminum hydride or sodium cyanoborohydride.
The hydrazone is subsequently reduced by sodium cyanoborohydride to produce a stable PEG conjugate.
