Examples of 'electrophiles' in a sentence
Meaning of "electrophiles"
electrophile (noun) - A term in chemistry referring to an atom or molecule that is attracted to an electron-rich center or has a tendency to accept an electron pair during a chemical reaction
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- plural of electrophile
How to use "electrophiles" in a sentence
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electrophiles
Many electrophiles are chiral and optically stable.
These anions react with a variety of electrophiles.
Useful electrophiles include a nitrogen containing electrophile.
The approach is particularly effective for electrophiles.
Preferred electrophiles are methyl iodide and hexachloroethane.
It is highly reactive toward electrophiles and free radicals.
Electrophiles attack the carbonyl oxygen.
Examples of appropriate electrophiles are shown in the table below.
Electrophiles react with nucleophiles to form covalent bonds.
Cyclic esters are formed upon treatment dichloro electrophiles.
Preferred electrophiles include methyl iodide and hexachloroethane.
Other compounds generate electrophiles in situ.
The preferred electrophiles are ethyl chloroformate or ethyl cyanoformate.
Fullerenes tend to react as electrophiles.
Preferred electrophiles of the present invention are carbon electrophiles.
See also
Enolate trapping with various electrophiles is decidedly less common.
Electrophiles accept these electrons.
Corannulene can react with electrophiles to form a corannulene carbocation.
Allyl shifts can also take place with electrophiles.
Fullerenes react as electrophiles with a host of nucleophiles in nucleophilic additions.
The intermediate enolboranes may also be quenched with electrophiles.
They can also act as electrophiles in electrophilic aromatic substitution.
Substitution reactions with electrophiles.
Preferred electrophiles as starting materials include methyl iodide and acetyl chloride.
Alkyl sulfonates are also used as electrophiles or are converted to alkyl halides.
These resins were not employed when isocyanates or isothiocyanates were used as electrophiles.
Alkyl sulfonates can be used as electrophiles or are converted to alkyl halides.
Singlet carbenes generally participate in cheletropic reactions as either electrophiles or nucleophiles.
These anions can be reacted with electrophiles to form a wide range of products.
Electrophiles are capable of forming single or double bonds vÃa electron transfer from a nucleophile.
These compounds are typically electrophiles that react with pathogens.
They undergo nucleophilic addition and substitution reactions with various electrophiles.
Alkyl sulfonates can also be used as electrophiles or can be converted to alkyl halides.
This strong nucleophile can then be used as such with other electrophiles.
The diazeniumdiolate anions react with electrophiles to produce stable covalent compounds.
This process may be conducted in a wide variety of solvents with a wide array of electrophiles.
Organothallium compounds generally react with electrophiles to form the monoalkylated products.
Substituted cyclopropenes can be deprotonated with alkyllithium reagents and reacted with electrophiles.
These anions may react with various electrophiles especially with halogenated compounds.
Hemoglobin contains several neutrophilic centers which undergo covalent reactions with electrophiles.
The modification pattern of the cysteine residues by electrophiles is known as the cysteine code.
These species form Grignard reagents that then can be treated with a variety of electrophiles.
It will further be understood that not all electrophiles will react with every nucleophile.
GST acts as a catalyst in the reaction between glutathione and its target electrophiles.
These secondary amines react more controllably with electrophiles than do the corresponding primary amines.
Heteroatom electrophiles Disulfide formation by reaction of Pyridyl disulfide with Mercaptanes.
Isothiocyanates are weak electrophiles.
Specific electrophiles of the following nature are included in the invention,.
Preferred reactive groups are selected from the group of electrophiles and nucleophiles.
Electrophiles are involved in electrophilic substitution reactions, particularly in electrophilic aromatic substitutions.
