Examples of 'cyclization reaction' in a sentence
Meaning of "cyclization reaction"
A cyclization reaction is a chemical process where a molecule undergoes a rearrangement to form a cyclic compound. This reaction involves the formation of bonds within the molecule to create a ring structure. Cyclization reactions are commonly used in organic synthesis to create complex molecules with specific structural features
How to use "cyclization reaction" in a sentence
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cyclization reaction
The cyclization reaction is performed in an organic acid.
It is then used in the cyclization reaction in this form.
The cyclization reaction was accomplished by three different procedures.
It is then employed in the cyclization reaction in this form.
The cyclization reaction may be conducted in a conventional manner.
The resulting reaction is a cyclization reaction.
An exemplary cyclization reaction is shown below.
This reaction mixture was directly subjected to cyclization reaction.
Intramolecular cyclization reaction between the two aromatic rings.
This mixture was directly used in the following cyclization reaction.
Solvents usable in the cyclization reaction are usable as the solvent.
Any suitable base may be used in the cyclization reaction.
The cyclization reaction is usually carried out in an appropriate solvent.
It is subsequently employed in the cyclization reaction in this form.
The cyclization reaction is normally carried out at ambient room temperature.
See also
Solvents can also be used to facilitate the cyclization reaction.
The cyclization reaction is usually performed in the presence or absence of a basic compound.
Ninhydrin analysis indicated that the cyclization reaction was complete.
This cyclization reaction is preferably carried out under acidic to neutral conditions.
The products were then subjected to a cyclization reaction without further treatment.
Rearrangement products are also formed in competition with the cyclization reaction.
The operation temperature during the cyclization reaction is not particularly restricted.
All of these latter peptides were competitive inhibitors of the cyclization reaction.
The intramolecular cyclization reaction proceeds by heating without using a reagent in particular.
Said resins can also be used for the cyclization reaction.
The cyclization reaction is preferably effected in the liquid or vapor states or mixtures thereof.
The resulting suspension can be subjected to the cyclization reaction directly.
The cyclization reaction can be conducted using either a gaseous or liquid phase reaction.
More preferably water is not present in the cyclization reaction medium.
This cyclization reaction is carried out with the cleavage from polystyrene resin.
Reactive distillation may be useful in conducting the cyclization reaction step.
This cyclization reaction can occur both in solid state and solution state.
Examples of the dehydrating agent used in this cyclization reaction are as given above.
The cyclization reaction temperature is preferably close to the reflux temperature of the solvent employed.
The temperature depends on the time for completing this cyclization reaction.
The cyclization reaction can be carried out at pressures both above and below atmospheric pressure.
Solvents described above for use in the cyclization reaction may be used as the solvent.
The compositions were held for various time periods before the start of the cyclization reaction.
The stabilization reaction includes a cyclization reaction with heat and an oxidation reaction with oxygen.
The dehydration of amide to nitrile can take place under carbonylation and cyclization reaction conditions.
The disulfide cyclization reaction was monitored by analytical HPLC.
This linear peptide is used directly for the next step cyclization reaction without purification.
This cyclization reaction can be achieved using variety of Palladium catalysts.
This demonstrates directly that the hydroxylation reaction in carotenoid biosynthesis occurs after the cyclization reaction.
The Nazarov cyclization reaction is a named electrocyclic reaction converting divinylketones to cyclopentenones.
Step 6 is a method of constructing a dihydroimidazopyridine ring by cyclization reaction.
This cyclization reaction is carried out with the cleavage of T group.
Trichotriol reacts in a non-enzymatic cyclization reaction to its isomere isotrichodermol.
This cyclization reaction is completed simultaneously with the cleavage of T group.
In certain embodiments, the cyclization reaction is performed in a solvent.
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The cyclization preferably takes place by heating
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Cyclization of the derivatives of general formula IIa
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