Examples of 'lithium aluminum hydride' in a sentence
Meaning of "lithium aluminum hydride"
is a powerful reducing agent used in organic chemistry for the reduction of various functional groups. It is commonly used for converting carbonyl compounds into alcohols
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- Alternative spelling of lithium aluminium hydride
How to use "lithium aluminum hydride" in a sentence
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lithium aluminum hydride
Reduction with lithium aluminum hydride is preferred.
The reducing agent is advantageously lithium aluminum hydride.
Lithium aluminum hydride is particularly preferred.
The preferred reagent is lithium aluminum hydride.
Lithium aluminum hydride is the preferred reducing agent.
An example of reducing agent is lithium aluminum hydride.
Lithium aluminum hydride is prefectly suitable to promote such a reaction.
A suitable reducing agent is lithium aluminum hydride.
Lithium aluminum hydride can be used as the reducing agent.
Tetrahydrofuran was dried by distillation over lithium aluminum hydride.
Purchase lithium aluminum hydride.
Preferably the reducing agent is lithium aluminum hydride.
Excess lithium aluminum hydride was carefully quenched with water.
Ethyl ether was distilled from lithium aluminum hydride prior to use.
Lithium aluminum hydride can also be used by itself as a solid fuel.
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Preferred metal hydrides are lithium aluminum hydride and aluminum hydride.
Lithium aluminum hydride and diborane are used as the reducing agent.
Also reducing agent such as lithium aluminum hydride can be used.
Lithium aluminum hydride and tetrahydrofuran is the preferred reaction medium.
From the acid derivatives by reduction with lithium aluminum hydride.
Lithium aluminum hydride reduction of alkyl substituted isoxazoles gave a variety of products.
These reduction conditions provide an alternative to a lithium aluminum hydride reduction.
Lithium aluminum hydride is the preferred reducing agent for the process.
The cyclic peptide is then reduced with lithium aluminum hydride.
Lithium aluminum hydride is illustrated in the synthetic example set forth below.
The ester was further reduced to alcohol using lithium aluminum hydride.
Excess lithium aluminum hydride was neutralized with a saturated ammonium chloride solution.
The resulting cyclic triamide is then reduced with lithium aluminum hydride.
Lithium aluminum hydride is the preferred reducing agent for this reaction.
This derivative is then reduced and detosylated with lithium aluminum hydride.
Lithium aluminum hydride and sodium borohydride are representative examples of suitable reducing agents.
Preferred metal hydride reducing agents include lithium aluminum hydride or sodium cyanoborohydride.
Excess lithium aluminum hydride is quenched with portions of ethyl acetate followed by water.
The reducing agent may be a known reducing agent such as lithium aluminum hydride.
Lithium aluminum hydride in an ether solvent such as tetrahydrofuran is preferred for this conversion.
The resulting macrocyclic diamide is reduced and detosylated with lithium aluminum hydride.
Lithium aluminum hydride and tetrahydrofuran are the preferred solvent and reducing agent.
Reduction of the amide with lithium aluminum hydride provides final cationic lipids viii.
The resulting cyclic amide is then reduced and detosylated with lithium aluminum hydride.
This reduction may be carried out using lithium aluminum hydride or other strong reducing agent.
Examples of the reagent used include general reducing agents such as lithium aluminum hydride.
The azide was reduced vía lithium aluminum hydride to the amine XX.
Citric acid can be added to bind with the aluminum from the lithium aluminum hydride.
Lithium aluminum hydride is preferred for the formation of compounds of formula XIII.
Suitable reducing agents for this transformation include lithium aluminum hydride and borane.
LAH is lithium aluminum hydride.
Compound XXII was reduced to the alcohol XXIII using lithium aluminum hydride.
Amide xiii can be reduced with lithium aluminum hydride in THF to afford aldehyde xiv.
The reducing agents are hydrogen, sodium borohydride or lithium aluminum hydride.
Suitable reducing conditions include lithium aluminum hydride and Raney nickel in conjunction with hydrogen.
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Sodium hydride or sodium amide is preferably used
The preferred metal hydride is sodium hydride
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Examples of using Aluminum
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