Examples of 'lithium aluminium hydride' in a sentence
Meaning of "lithium aluminium hydride"
Lithium aluminium hydride: Lithium aluminium hydride is a powerful reducing agent used in organic chemistry for the reduction of various compounds
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- LiAlH₄, a powerful reducing agent with many applications in organic chemistry; contains the aluminohydride anion AlH₄⁻.
How to use "lithium aluminium hydride" in a sentence
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lithium aluminium hydride
Lithium aluminium hydride is the preferred reducing agent.
The reducing agent may be lithium aluminium hydride.
Lithium aluminium hydride may be mentioned as a reducing agent.
Suitable reducing agent include lithium aluminium hydride or borane.
Lithium aluminium hydride does not reduce simple alkenes or arenes.
This is then reduced to a diol with lithium aluminium hydride.
Lithium aluminium hydride also reduces alkyl halides to alkanes.
The hydrogenation is preferably performed using lithium aluminium hydride.
Lithium aluminium hydride is the most suitable reducing agent.
This solution was then reduced with lithium aluminium hydride.
Lithium aluminium hydride is widely used in organic chemistry as a reducing agent.
An example for a suitable hydride reagent is lithium aluminium hydride.
Subsequent reduction with lithium aluminium hydride afforded the title compound.
These reactions can be effected stoichiometrically using lithium aluminium hydride.
Preferably the metal hydride is lithium aluminium hydride or sodium aluminium hydride.
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Suitable reducing agents include sodium borohydride or lithium aluminium hydride.
Reduction of camphoric carbonyl by lithium aluminium hydride in tetrahydrofuran to afford corresponding alcohol.
Using a metal hydride reducing agent such as lithium aluminium hydride.
Ether was distilled from lithium aluminium hydride and stored over sodium wire.
Preferably the reaction is carried out with lithium aluminium hydride.
Reduction of an epoxide with lithium aluminium hydride or aluminium hydride produces the corresponding alcohol.
More preferably the metal hydride is lithium aluminium hydride.
Subsequent reduction with lithium aluminium hydride in dioxane at room temperature yields the targeted amines.
This reaction is used as an industrial alternative to lithium aluminium hydride reduction.
If necessary, lithium aluminium hydride may be added.
Suitable reducing agents include sodium borohydride and lithium aluminium hydride.
Examples of suitable reducing agents include lithium aluminium hydride and suitable inert solvents include tetrahydrofuran.
A suitable reducing agent for effecting this transformation is lithium aluminium hydride.
The ester groups were then reduced by lithium aluminium hydride to a triol in a deprotection step.
A suitable reducing agent is a complex metal hydride such as lithium aluminium hydride.
Reduction with lithium aluminium hydride in tetrahydrofuran, and.
Diborane is used as a reducing agent roughly complementary to the reactivity of lithium aluminium hydride.
The " LiAlHSH " is prepared by treating lithium aluminium hydride with elemental sulfur.
Excess lithium aluminium hydride was destroyed by careful addition of a saturated Na2SO4 solution.
If required, further portions of lithium aluminium hydride are added.
Lithium aluminium hydride ( LiAlH 4 ) is commonly used as a reducing agent in organic synthesis.
Preferably, the reducing agent is lithium aluminium hydride.
Afterwards the lithium aluminium hydride excess is destroyed with water and 15 % sodium hydroxide.
In one embodiment, the reducing agent is lithium aluminium hydride.
Such agents are, for example, lithium aluminium hydride or other complex aluminium hydrides.
Starting with acid derivatives, by reduction with lithium aluminium hydride.
Reduction of ( ± ) arylated methyl ketopinate by lithium aluminium hydride in tetrahydrofuran to afford corresponding alcohol ;.
The process an claimed in claim 2, wherein the hydride is lithium aluminium hydride.
To this mixture was added lithium aluminium hydride ( 1 g ) in one lot.
A process according to claim 12 wherein the reduction is effected by lithium aluminium hydride.
Reduction with lithium aluminium hydride ( LAH ) afforded alcohol 2.
Sulfonyl groups can be reduced to the hydrocarbon with lithium aluminium hydride LiAlH4.
Reduction with lithium aluminium hydride in a aprotic solvent such as THF furnished the desired alcohol ( 15 ).
The reducing agent used in process c is preferably lithium aluminium hydride or diisobutyl-aluminium hydride.
D, Lithium aluminium hydride.
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