Examples of 'diisobutylaluminum hydride' in a sentence

Meaning of "diisobutylaluminum hydride"

diisobutylaluminum hydride - a chemical compound commonly used in organic synthesis as a reducing agent

How to use "diisobutylaluminum hydride" in a sentence

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diisobutylaluminum hydride
Preferred reducing agents include diisobutylaluminum hydride.
Among them, diisobutylaluminum hydride and triisobutylaluminum are preferred.
The preferred reagent is diisobutylaluminum hydride.
Suitable hydride reducing agents include lithium aluminum hydride, lithium borohydride, sodium borohydride, and diisobutylaluminum hydride.
Reduction of ethyl geranylgeranoate with diisobutylaluminum hydride provides GG cleanly.
Throughout the application the following abbreviations are used with the following meanings, DIBAL Diisobutylaluminum hydride.
As the reducing agent, diisobutylaluminum hydride is suitably used.
Alkylaluminum hydrides such as diethylaluminum hydride or diisobutylaluminum hydride.
Preferably, diisobutylaluminum hydride is used.
Dialkylaluminum hydrides, for example diisobutylaluminum hydride.
Then 2 more equivalents of diisobutylaluminum hydride are added and the reaction is warmed to 50 °.
A process according to claim 2 where the reducing agent is diisobutylaluminum hydride.
Alternatively, a hydride donor such as diisobutylaluminum hydride ( DIBAL ) can be used as the reducing agent.
Such reducing agents include, but are not limited to, diisobutylaluminum hydride.
This is further reduced by diisobutylaluminum hydride to give the lactol ( 53 ).

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In this case, examples of the metal hydride include diisobutylaluminum hydride.
In step two, reduction of 5 with diisobutylaluminum hydride ( DIBAL ) in methylene chloride gives the diol 6.
The method according to claim 2, wherein said alkylaluminum compound is diisobutylaluminum hydride.
Under argon, 4.65 ml of a 1 M solution of diisobutylaluminum hydride in hexane were slowly added.
The process according to claim 6, characterized in that the alkylaluminum compound is diisobutylaluminum hydride.
Examples of such reducing agents include, diisobutylaluminum hydride and sodium borohydride.
Alternatively, the trans-cinnamates may be reduced to ( E ) - allylic alcohols by the use of diisobutylaluminum hydride.
Most preferably, the reducing agent is diisobutylaluminum hydride ( DiBAL-H ) in toluene.
The reduction of the compound ( b ) is preferably carried out by reacting diisobutylaluminum hydride.
Reduction of 15a with diisobutylaluminum hydride ( DIBAL-H ), lithium aluminum hydride or lithium triethylborohydride affords the diol 15b.
Among these compounds, diethylaluminum hydride, and diisobutylaluminum hydride are preferable.
Other useful reducing agents include diisobutylaluminum hydride ( DIBAL-H, 2 equivalents ), borane-THF complex, and the like.
For example, heteroarylester can be reduced to the aldehyde by treatment with diisobutylaluminum hydride.
To this mixture was added 67 ml of 1M diisobutylaluminum hydride ( DIBAL ) in tetrahydrofuran.
A process according to claim 14, wherein the reducing agent is diisobutylaluminum hydride.
Among them, lithium aluminum hydride and diisobutylaluminum hydride are preferred.
The process of Claim 2 wherein atropisomer 2.1A is reduced using diisobutylaluminum hydride.
The term DIBAL-H means diisobutylaluminum hydride.
The method of Claim 21 wherein the reducing agent is diisobutylaluminum hydride.
As the " reductant ", lithium aluminum hydride, diisobutylaluminum hydride and the like can be used.
The method of Clam 20 wherein the reducing agent is diisobutylaluminum hydride.
The reduction of benzyl ester is carried out using diisobutylaluminum hydride ( DIBAL-H ) in toluene.
G of the compound ( 15 ) are reduced with 3 equivalents of diisobutylaluminum hydride.
Then, the reaction solution was cooled to -5°C, and excess diisobutylaluminum hydride was decomposed with ethanol.
Removing the vinylacetylene compounds ( residual “ true ” alkynes ) by distillation on diisobutylaluminum hydride ( DiBAH ), and.
As the " reductant ", lithium aluminum hydride, diisobutylaluminum hydride can be used.
Reduction of Example 335 with reagents such as diisobutylaluminum hydride provided Example 336.

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