The phrase "aromatic ester" is correct and usable in written English.
It can be used in contexts related to chemistry, specifically when discussing compounds that are esters derived from aromatic acids.
Example: "The synthesis of the aromatic ester resulted in a compound with a distinct floral fragrance."
Alternatives: "fragrant ester" or "aromatic compound".
In this case, a possible explanation for this shifting could be the fact that the esteric group suffers a chemical modification, with the transformation of the aromatic ester into an aliphatic one due to the presence of stearate anion or leading to the formation of p-aminobenzoic acid, due to the hydrolysis of ester by the presence of HCl.
We have also investigated the influence of aromatic ester substituents on inhibitory potency towards SplB.
Moreover, this system incorporates an aromatic ester functionality suitable for bioconjugation.
These polymers contain aromatic ester groups which undergo a photo-Fries rearrangement from aryl esters to hydroxyketones.
Main-chain liquid-crystalline polymers containing triad aromatic ester mesogenic blocks together with flexible ion-complexing oligo-oxyethylene blocks have been synthesized.
This is attributed to motions of non-substituted aromatic ester species including 4-hydroxybenzoic acid (HBA) due to their relatively low barriers to rotation.
The alkaline hydrolysis of aromatic esters exhibits auto-accelerated kinetics when performed under two phase conditions.
In addition, it is found that both aromatic and aliphatic alcohols can inhibit the oxidation of the substrates and other intermediates (aromatic esters, aromatic aldehydes).
This platform expanded the capabilities of bacterial production of high-value natural aromatic esters and amides from renewable carbon source via tailoring non-natural biosynthetic pathways.
Moreover, the oxidative esterifications of isovanillin, syringaldehyde, p-anisaldehyde and 3, 4, 5- trimethoxybenzaldehyde were successfully performed, and 70.2 98.0% yields of methyl aromatic esters are obtained.
These studies provided the evidence for future design of novel antimigratory compounds based on a simplified sipholane structure possessing rings A and B (perhydrobenzoxepine) connected to substituted aromatic esters, with the elimination of rings C and D ([5,3,0]bicyclodecane system).
