Examples of 'sodium triacetoxyborohydride' in a sentence
Meaning of "sodium triacetoxyborohydride"
sodium triacetoxyborohydride - Sodium triacetoxyborohydride is a chemical compound commonly used as a reducing agent in organic synthesis. It is particularly effective for the reduction of aldehydes and ketones to their respective alcohols under mild conditions
How to use "sodium triacetoxyborohydride" in a sentence
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sodium triacetoxyborohydride
Sodium triacetoxyborohydride is the preferred reducing agent.
Preferred first reducing agent is sodium triacetoxyborohydride.
Using sodium triacetoxyborohydride or sodium cyanoborohydride.
For example in several cases sodium triacetoxyborohydride was used.
Sodium triacetoxyborohydride is generally used as the reducing agent.
The preferred borohydride is sodium triacetoxyborohydride.
Sodium triacetoxyborohydride is preferred.
A second reductive amination was run using sodium triacetoxyborohydride.
Add sodium triacetoxyborohydride portionwise and stir the mixture at room temperature overnight.
Preferred reducing agents are sodium cyanoborohydride or sodium triacetoxyborohydride.
Sodium borohydride and sodium triacetoxyborohydride may also be used.
Preferred hydride reducing agents include sodium cyanoborohydride or sodium triacetoxyborohydride.
Suitable reducing agents include sodium triacetoxyborohydride and sodium cyanoborohydride.
Examples of a reducing agent include sodium borohydride and sodium triacetoxyborohydride.
A hydride reducing agent such as sodium triacetoxyborohydride followed by deprotection of the amino group.
See also
A preferable reducing agent in this reaction is sodium triacetoxyborohydride.
Preferred conditions use sodium triacetoxyborohydride in an inert solvent such as dichloromethane or THF.
Suitable reducing agents include borohydrides such as sodium cyanoborohydride or sodium triacetoxyborohydride.
Preferred conditions involve the use of sodium triacetoxyborohydride in tetrahydrofuran and acetic acid.
The reaction proceeds in the presence of a reducing agent such as sodium triacetoxyborohydride.
Alternatively, sodium triacetoxyborohydride or sodium cyanohydride may be used.
The reaction is carried out in presence of sodium triacetoxyborohydride and acetic acid.
Of these, sodium triacetoxyborohydride is preferred.
A more preferred embodiment of the invention is where the reducing agent is sodium triacetoxyborohydride.
In some case reducing agents other than sodium triacetoxyborohydride can be used in the reaction.
Sodium triacetoxyborohydride is added and the reaction mixture is stirred overnight at r . t.
Preferably, the reducing agent is sodium triacetoxyborohydride.
Among those, sodium triacetoxyborohydride is preferred.
In some embodiments, the reducing agent is sodium triacetoxyborohydride.
In some embodiments, sodium triacetoxyborohydride and trifluoroacetic acid may be used.
Over a period of 5 hours a further 3 equivalents of sodium triacetoxyborohydride were added.
Suitable solvents for sodium triacetoxyborohydride include aprotic organic solvents such as tetrahydrofuran, acetonitrile or dichloroethane.
A borohydride such as sodium borohydride, sodium cyanoborohydride or sodium triacetoxyborohydride.
Of these, we prefer sodium triacetoxyborohydride.
In a particular embodiment, the first reducing agent may be sodium borohydride or sodium triacetoxyborohydride.
Preferably, the reducing agent is sodium triacetoxyborohydride or sodium borohydride.
Typical reducing agents include sodium borohydride, lithium borohydride, and sodium triacetoxyborohydride.
Reductive amination with sodium triacetoxyborohydride will produce compounds IV-8.
In one particular embodiment, the reducing agent is sodium triacetoxyborohydride.
Preferably, the reducing agent is sodium triacetoxyborohydride and the solvent is acetic add in THF.
The solid dissolved, acetone was added, followed by sodium triacetoxyborohydride.
Further 42 mg of sodium triacetoxyborohydride was added, followed by stirring overnight.
Of these agents, sodium cyanoborohydride and sodium triacetoxyborohydride are preferred.
Added more sodium triacetoxyborohydride ( 5 mg ) and stirred at rt overnight.
Preferably, the reductive amination is carried out using sodium triacetoxyborohydride.
To this solution was added sodium triacetoxyborohydride ( 1.5 eq ) followed by a catalytic amount of acetic acid.
A process according to claim 2, wherein said reducing agent is sodium triacetoxyborohydride.
In a particularly preferred embodiment, sodium triacetoxyborohydride in DCE is employed at room temperature.
A process of claim 6 wherein the hydride reducing agent is sodium triacetoxyborohydride.
Sodium triacetoxyborohydride ( 17 mg ) was added to the reaction and stirring continued for two hours.
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Examples of using Triacetoxyborohydride
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Sodium triacetoxyborohydride is the preferred reducing agent
Preferred first reducing agent is sodium triacetoxyborohydride
Using sodium triacetoxyborohydride or sodium cyanoborohydride
