Examples of 'claisen' in a sentence
Meaning of "claisen"
Claisen (verb): It may refer to a chemical reaction or process named after the chemist Rainer Ludwig Claisen. It is commonly used in the field of organic chemistry
How to use "claisen" in a sentence
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claisen
Claisen rearrangement of allyl esters.
Method for producing bicyclic compound via claisen rearrangement.
Claisen ester condensations.
The reason we have discussed why meta product is not possible in claisen rearrangement.
Claisen ester condensation.
They can be formed by the Claisen condensation.
A Claisen condensation involves two ester compounds.
The reaction is known as the Claisen condensation.
A Claisen distillation head was attached to the reaction vessel.
It is prepared via the Claisen condensation of ethyl acetate.
The equivalent intermolecular reaction is the Claisen condensation.
The Claisen rearrangement reaction is conducted by heating in a suitable solvent.
One experiment that it is used for is the Claisen rearrangement.
One joint of the Claisen adapter was connected to the nitrogen inlet.
Allyloxyanthraquinones showed unusual behaviour during the Claisen rearrangement.
See also
Prephenic acid is then synthesized by a Claisen rearrangement of chorismate by Chorismate mutase.
By hydrolysis of the corresponding esters prepared via the Claisen transformation.
The orthoester Claisen rearrangement in the preparation of hirsutine type indole alkaloids.
The reaction between two esters is called the Claisen condensation.
These reactions are essentially Claisen reactions and well known to the practitioners.
This method was found to be more effective than thermal Claisen rearrangement.
This approach is based on a Claisen type condensation of suitable precursors as a key reaction step.
The analogue reaction for esters is called the condensation of Claisen.
Sodium ethoxide is commonly used in the Claisen condensation and malonic ester synthesis.
This approach is used to study the solvent effects in the Claisen reaction.
A Claisen adapter was used to incorporate the thermometer and the nitrogen sweep inlet.
The nitrogen inlet on the reaction flask was replaced with a Claisen adapter.
The Claisen reaction can take from one to eight hours with three hours usually sufficient.
This reaction was discovered by a happy chance by great German chemist Ludwig Claisen.
The other arm of the Claisen adapter was topped with a Dewar condenser.
Claisen condensation Gabriel-Colman rearrangement.
It is biosynthesized by a - sigmatropic Claisen rearrangement of chorismate.
A three-way claisen adapter was attached to the open end of the reactor.
In his honor, the reaction has been named the Claisen rearrangement.
On the other hand, the Claisen rearrangement reaction itself is a known reaction.
In nature, polyketides are synthesized by enzymes that effect iterative Claisen condensations.
Step 2 is Claisen rearrangement either by heating or by a Lewis acid treatment.
Designer of a special distillation flask, now known as the Claisen flask.
Compound ( VIIIb ) is produced by the Claisen rearrangement reaction of compound ( VIIb ).
The pulegone was functionalized, and the lateral chain was installed by a Claisen rearrangement.
Orthoester Claisen rearrangement in the syntheses of 3-epi-corynantheine-type indole alkaloids.
Like many other esters, this compound undergoes the Claisen ester condensations.
In the present invention, the Claisen rearrangement reaction is induced in the compound ( 2 ).
The other prevalent class of sigmatropic rearrangements are, notably the Cope and Claisen rearrangements.
Key words, aluminum chloride, sequential Claisen rearrangement, hydroaryloxylation, furothiopyran, pyrimidine.
Combine the extracts and remove the water by co-distillation with benzene through a modified Claisen flask.
Acetyl-CoA and malonyl-CoA undergo a Claisen condensation with lose of carbon dioxide to form acetoacetyl-CoA.
The thiolase superfamily enzymes catalyse the carbon - carbon-bond formation via a thioester-dependent Claisen condensation reaction mechanism.
Later, another SxtA performs a Claisen condensation reaction between propionyl-ACP and arginine producing intermediate 4 and intermediate 3.
These B-ketoesters are formed as a result of a Claisen condensation.
