Examples of 'aromatic aldehydes' in a sentence
Meaning of "aromatic aldehydes"
aromatic aldehydes: This term is often used in the field of chemistry to describe a specific group of organic compounds with distinct smells or odors
How to use "aromatic aldehydes" in a sentence
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aromatic aldehydes
Process for the preparation of aromatic aldehydes.
Other aromatic aldehydes are also used.
Process for production of aromatic aldehydes.
Some aromatic aldehydes are components of natural products as well.
These substrates need not to be limited to aromatic aldehydes.
Many contain aromatic aldehydes such as vanillin and benzaldehyde.
The reaction generally occurs between aromatic aldehydes or glyoxals.
Not all aromatic aldehydes yield phenols according to this reaction.
And a variety of methods are known for brominating aromatic aldehydes.
These types of subsituted aromatic aldehydes are therefore most preferred.
Several methods are reported for the synthesis of aromatic aldehydes.
Aromatic aldehydes have identical properties and side effects as phenols.
Of particular interest are aromatic aldehydes.
Aromatic aldehydes which may be used include benzaldehyde and salicylaldehyde.
Preparation of aromatic aldehydes.
See also
Various processes have been proposed for the synthesis of aromatic aldehydes.
Such aromatic aldehydes result from renewable resources and not from oil.
The ligands are typically derived from alkyl diamines and aromatic aldehydes.
The aromatic aldehydes are generally employed as isolated compounds mixed with a suitable carrier.
The first methods were only suitable for the conversion of aromatic aldehydes.
Many aromatic aldehydes are known materials that commonly find use as chemical intermediates.
The molecule is structurally related to other aromatic aldehydes such as benzaldehyde and vanillin.
Another useful class of phenolic resins of the present invention is based on aromatic aldehydes.
It is known to prepare aromatic aldehydes according to at least two types of methods,.
Synthesis of the imines was accomplished by condensing commercially available aromatic aldehydes and sulfonamides.
With aromatic aldehydes such as benzaldehyde, the benzoin condensation is a competing reaction.
Both enzymes exhibited a broad substrate specificity oxidizing a wide variety of aliphatic and aromatic aldehydes.
Aromatic aldehydes are broadly used also for applications to polyurethane-based sealants.
State of the Art This invention involves the use of aromatic aldehydes.
Additionally, various aromatic aldehydes can be prepared by reduction of the corresponding aryl nitriles.
Both substituted and unsubstituted, carbocyclic and heterocyclic aromatic aldehydes can be used.
Aromatic aldehydes were purchased from Aldrich Chemical Company, as were all other chemicals.
However, derivatives and analogs of vanillin and other aromatic aldehydes can be used also.
Examples of aromatic aldehydes include benzaldehyde and 3-nitrobenzaldehyde.
In their work the authors have primarily concentrated on the aromatic aldehydes ( cinnamaldehyde and veratraldehyde ).
Numerous aromatic aldehydes are also commercially available, such as, for example,.
Examples thereof include aliphatic aldehydes and acetals, terpene aldehydes and acetals, aromatic aldehydes and acetals.
Suitable aromatic aldehydes include benzaldehyde, anisaldehyde, dimethoxybenzaldehyde, preferred is benzaldehyde.
Their best ligand: The disadvantage is that the substrate can only be aromatic aldehydes.
Described the condensation of aromatic aldehydes with aliphatic aldehydes or ketones in 1881.
Aldehydes such as OPA ( ortho-phthalaldehyde ), glutaldehyde, and aromatic aldehydes are suitable.
Dihydroxylation and oxidation give the aromatic aldehydes 13 that can be reductively aminated to provide amines 14.
Aromatic aldehydes produce almost exclusively ( E ) - alkenes.
Process for the preparation of aromatic aldehydes ( I ) starting from 8-methoxycuminic aldehyde.
The reaction generally occurs between aromatic aldehydes or glyoxals . [ 1 ] [ 2 ] The reaction produces an acyloin.
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Acyclic aldehydes without other oxygen function
Coli to convert other aldehydes into alcohols
Cyclic aldehydes without other oxygen function
