Examples of 'diels-alder' in a sentence
Meaning of "diels-alder"
Diels-Alder is an adjective describing a type of chemical reaction between a conjugated diene and an alkene, creating a cyclohexene derivative
How to use "diels-alder" in a sentence
Basic
Advanced
diels-alder
The Diels-Alder reaction is a pericyclic reaction.
This is an example of a hexadehydro Diels-Alder reaction.
They undergo Diels-Alder reaction with dienes.
It may be used as a catalyst in Diels-Alder reactions.
The Diels-Alder reaction is performed in an organic solvent.
Regiochemistry and stereochemistry in diels-alder reactions.
Microbial transformation of diels-alder cycloadducts were trailed by the endophyte p.
Norbornadiene is also a useful dienophile in Diels-Alder reactions.
It is prepared by the Diels-Alder reaction of butadiene and cyclopentadiene.
Maleic anhydride is a dienophile in the Diels-Alder reaction.
Norbornene is made by a Diels-Alder reaction of cyclopentadiene and ethylene.
Naphthoquinone acts as strong dienophile in Diels-Alder reaction.
It is the formal Diels-Alder adduct of benzene and acetylene.
Cyclohexenes often undergo retro Diels-Alder reactions.
Intramolecular Diels-Alder reactions have been observed in this context.
See also
The cycloaddition may be a Diels-Alder reaction.
Attempted retro Diels-Alder reactions of the thiophenes were unsuccessful.
They undergo inverse demand Diels-Alder reactions.
The retro Diels-Alder reaction is used in the industrial production of cyclopentadiene.
Nitrosobenzene undergoes Diels-Alder reactions with dienes.
Chlorendic acid is industrially produced in high volumes by Diels-Alder reaction.
Abietic acid undergoes Diels-Alder addition with dienophiles.
They are commonly employed as dienophiles in the Diels-Alder reaction.
The reaction is a stepwise Diels-Alder like reaction, forming a carbocation as intermediate.
Synthesis of glutaraldehyde via the Diels-Alder reaction.
The first Diels-Alder addition of a diene to a cyclooctenone dienophile has been observed.
Such reactions are generally believed to be Diels-Alder reactions.
Norbornadiene can be formed by a Diels-Alder reaction between cyclopentadiene and acetylene.
Unsaturated aldehydes can be prepared by the Diels-Alder reaction.
The Diels-Alder type arsolidinium adduct is structurally characterized crystal data,.
The aldehyde may be prepared vÃa Diels-Alder chemistry.
The Diels-Alder reaction between a dienophile 6 and cyclopentadiene was therefore studied.
Enones are often good dienophiles in Diels-Alder reactions.
The effluent from the Diels-Alder reactor was fed to a distillation column.
The most important of these is the Diels-Alder reaction.
The Diels-Alder reaction is an additive reaction of an olefin with a conjugated diene.
An important reaction for conjugated dienes is the Diels-Alder reaction.
This Diels-Alder adduct was converted in five steps into the title compound.
Himbacine has been synthesized using a Diels-Alder reaction as a key step.
The Diels-Alder reaction may be performed in the absence or in the presence of a solvent.
Thermoreversible networks were obtained by a Diels-Alder involving furan-maleimide couple.
The Diels-Alder reaction of cyclopentadiene with furan can produce two isomeric products.
Several tetracyclic molecules were prepared by diene-transmissive Diels-Alder cycloadditions.
This liquid is used as a catalyst in a Diels-Alder reaction of cyclopentadiene with methyl acrylate.
The solution is used directly in the following Diels-Alder reaction.
After cooling the Diels-Alder adduct was isolated by extraction with ethyl acetate.
These compounds can be prepared by utilizing the Diels-Alder reaction.
The chlordane starting material is prepared by the Diels-Alder condensation of hexachlorocyclopentadiene with cyclopentadiene.
It is not necessary to use a catalyst to advance the Diels-Alder reaction.
Unusual thermal Diels-Alder reactivity of arenes can be found in the Wagner-Jauregg reaction.
