Examples of 'diels-alder reactions' in a sentence

Meaning of "diels-alder reactions"

diels-alder reactions: Refers to a type of chemical reaction named after Otto Diels and Kurt Alder that involves the formation of a cyclic compound
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  • plural of Diels-Alder reaction

How to use "diels-alder reactions" in a sentence

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diels-alder reactions
It may be used as a catalyst in Diels-Alder reactions.
Intramolecular Diels-Alder reactions have been observed in this context.
Regiochemistry and stereochemistry in diels-alder reactions.
Attempted retro Diels-Alder reactions of the thiophenes were unsuccessful.
Norbornadiene is also a useful dienophile in Diels-Alder reactions.
Diels-Alder reactions have also been used to give access to functional derivatives.
Nitrosobenzene undergoes Diels-Alder reactions with dienes.
The hydrocarbon terpene is selected to have a stereochemistry amenable to Diels-Alder reactions.
Singlet oxygen can participate in Diels-Alder reactions and ene reactions.
This mesophase was subsequently used as reaction medium for intramolecular Diels-Alder reactions.
Diels-Alder reactions can lead to formation of a variety of structural isomers and stereoisomers.
They undergo inverse demand Diels-Alder reactions.
Diels-Alder reactions can produce diastereomers called endo and exo products.
Cyclohexenes often undergo retro Diels-Alder reactions.
These Gp are obtained using Diels-Alder reactions of acetylene derivatives with protoporphyrin under appropriate conditions.

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Such reactions are generally believed to be Diels-Alder reactions.
Diels-Alder reactions of pentenone with methylpentadiene.
Enones are often good dienophiles in Diels-Alder reactions.
Diels-Alder reactions of.
The calculated? values were compared with other photooxidation and Diels-Alder reactions.
For example, they undergo Diels-Alder reactions with electrophilic alkynes.
Because the diene is very electron-rich it is a very reactive reagent in Diels-Alder reactions.
Furan serves as a diene in Diels-Alder reactions with electron-deficient dienophiles such as ethyl ( E ) -3-nitroacrylate.
The bonds of fullerenes react as dienes or dienophiles in cycloadditions for instance Diels-Alder reactions.
CHT behaves as a diene in Diels-Alder reactions.
The catalytic activity of the more promising models has been studied in Diels-Alder reactions.
Table 1, Optimization of reaction conditions and yields of Diels-Alder reactions of the compound of formula 3a.
It is suggested that such compounds are useful as vehicles for carrying out Diels-Alder reactions.
The significance of the regiochemical and stereochemical results of the Diels-Alder reactions is discussed.
Iron carbonyls are used as a protective group for dienes in hydrogenations and Diels-Alder reactions.
With simple dienophiles, dendrales can give quick access to complex molecules in Diels-Alder reactions.
This result is unexpected since these trimers are not inert to additional thermal Diels-Alder reactions.
Maleic acid, being electrophilic, participates as a dienophile in many Diels-Alder reactions.
Acrylonitrile and derivatives, such as 2-chloro-acrylonitrile, are dienophiles in Diels-Alder reactions.
Metal ions are frequently a component of 1,3-dipolar cycloadditions, and Diels-Alder reactions.

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Examples of using 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
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