Examples of 'mitsunobu' in a sentence
Meaning of "mitsunobu"
mitsunobu (noun): A term not commonly used in English, perhaps being a name, technical term, or reference to a specific cultural concept or entity
How to use "mitsunobu" in a sentence
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mitsunobu
Mitsunobu conditions include those given above.
This process is known in the art as a Mitsunobu coupling.
Mitsunobu reaction is performed in an appropriate solvent.
This ether link preferably is formed vía a Mitsunobu reaction.
Mitsunobu reactions are well know to those skilled in the art of organic synthesis.
The chiral conversion is effected using a Mitsunobu reaction.
Mitsunobu reaction has several applications in the synthesis of natural products and pharmaceuticals.
The reaction mechanism of the Mitsunobu reaction is fairly complex.
Classical Mitsunobu conditions employ triphenylphosphine and diethyl azodicarboxylate.
The reaction mechanism of the Mitsunobu reaction is a bit complex.
Then a Mitsunobu reaction with alcohol afforded the ether.
The reaction is analogous to the well known Mitsunobu reaction.
Preferably the Mitsunobu reaction mixture comprises toluene.
The reaction portrayed is a known in the art as a Mitsunobu reaction.
The Mitsunobu product is then reduced to the aniline vía palladium on carbon.
See also
This material can be used as is in the following Mitsunobu step.
The Mitsunobu reaction can be carried out according to standard methods.
We find it convenient to perform a nucleophilc substitution reaction or a Mitsunobu reaction.
A Mitsunobu step is substituted for the alkylation step as described below.
In many cases the alcohols are converted to a phthalimide vía the Mitsunobu protocol.
The Mitsunobu adduct must then be deprotected to prepare the final product.
This reaction can be carried out by using the Mitsunobu reaction.
Examples of the Mitsunobu reagent include diethyl azodicarboxylate and diisopropyl azodicarboxylate.
The reaction is carried out in an inert solvent under standard Mitsunobu conditions.
This reaction can also be done through Mitsunobu displacement through hydroxyalkyl group.
The Mitsunobu reaction yields the final products with inversion of configuration.
The use of thiols or amines in the Mitsunobu reaction can give additional derivatives.
Variation on these conditions will be apparent from the literature on the Mitsunobu reaction.
Alcohol derivatives required for the Mitsunobu reactions are obtained by several different routes.
Silica gel chromatography is often required for the purification of coupling product of a Mitsunobu reaction.
The Mitsunobu reaction changes the stereochemical configuration at the carbon bearing the hydroxy group.
The skilled artisan will recognize that there are various Mitsunobu conditions employed in the art.
A Mitsunobu reaction can be used to install the Cy group.
Another pathway involves the Mitsunobu reaction.
Alternatively Mitsunobu conditions can be used.
When Y is a hydroxyl group the reaction is performed under Mitsunobu conditions.
This Mitsunobu reaction was performed analogously to step vi in scheme XIII.
Coupling reaction under Mitsunobu conditions.
Mitsunobu reaction with hydroxyphthalimide gives Compound XXIX.
The preparation of amidates by means of the Mitsunobu reaction is described in J.
Details of Mitsunobu reactions are contained in Tet.
Ring substituent, stereochemistry and ring variations series were prepared by mitsunobu reaction.
It should be noted that the Mitsunobu Reagent is readily decomposed by moisture.
The latter intermediate was prepared using Mitsunobu chemistry,.
Compound XXVII is subjected to Mitsunobu condition with hydroxyphthalimide to obtain Compound XXVIII.
Alternatively, it can be also achieved by carrying out Mitsunobu reaction.
However, the mitsunobu reaction suffers from many disadvantages.
With an imide or azide nitrogen nucleophile under Mitsunobu conditions ;.
Particularly, the Mitsunobu reaction is preferable.
Alternatively, alkylation of the benzaldehyde is carried out using a Mitsunobu reaction.
