Examples of 'leaving groups' in a sentence
Meaning of "leaving groups"
in the context of organic chemistry, refers to atoms or groups of atoms that can detach or dissociate from a molecule during a reaction. They are called leaving groups because they depart with a pair of electrons, often leaving behind a positive or partially positive charge on the molecule they were initially attached to
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- plural of leaving group
How to use "leaving groups" in a sentence
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leaving groups
Good leaving groups give fast reactions.
Especially preferred are phenol sulphonate leaving groups.
Leaving groups can be anions or neutral molecules.
Methyl or chloride leaving groups are most preferred.
Leaving groups are well known in the art.
Examples of appropriate leaving groups are described above.
Especially preferred are phenol sulfonate leaving groups.
Suitable leaving groups are known in the art.
These groups are known to be reactive leaving groups.
Suitable leaving groups are bromine and triflate.
Selection of substituents capable of functioning as leaving groups.
Such leaving groups are known in the art.
Such readily displaced substituents are commonly referred to as leaving groups.
Suitable leaving groups will be exemplified hereinafter.
Halogens are particularly suitable leaving groups for this reaction.
See also
Typical leaving groups are halide and sulfonate.
Halogens are particularly suitable leaving groups for these reactions.
Good leaving groups are weak bases.
The tosyl and mesyl groups are preferable leaving groups.
Preferred leaving groups are indicated herein where appropriate.
The skilled person will be familiar with suitable leaving groups.
Other leaving groups can be introduced by standard procedures.
Common neutral molecule leaving groups are water and ammonia.
Such leaving groups may be prepared separately or in situ.
Synthetic substrates containing flurogenic or chromogenic leaving groups can be used.
Suitable leaving groups include halogens.
X are independently leaving groups.
Preferable leaving groups in the reaction include halogen.
It is well known that acridinium esters with poor leaving groups are poorly chemiluminescent.
Suitable leaving groups are known to those skilled in the art.
The determined specific substrate is labeled with a plurality of chromatogenic or fluorescent leaving groups.
The preferred halogen leaving groups are bromide and iodide.
Leaving groups for displacement by thiol are known in the art.
Halogens are preferred leaving groups and bromo is especially preferred.
Leaving groups are well known to the person skilled in the art.
Aulogens are preferred leaving groups and bromo is especially preferred.
Leaving groups other than chloride may of course be used throughout.
Most preferred of the leaving groups is the phenol sulphonate type.
Leaving groups typically include those groups that can stabilize an anion.
These groups are good leaving groups and are therefore easily replaced.
Leaving groups include but are not limited to halogens and arylsulfonyloxy groups.
The use of better thioester leaving groups resulted in faster ligation reactions.
Leaving groups are groups which can easily be cleaved in nucleophilic substitution reactions.
Each of these preferred leaving groups will now be more specifically described.
Leaving groups are substituents which can be displaced by a nucleophilic moiety with relative ease.
Preferable examples of the leaving groups for the present reaction include halogen atoms.
Studies have been shown that the pathways differ by using different halogen leaving groups.
Especially preferred leaving groups are mentioned in the individual processes.
It is believed that this enhanced reactivity permits the flexibility of choice for leaving groups.
Other leaving groups will be apparent to the skilled artisan.
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Sorry for not leaving any marks
Leaving marks not to get ourselves lost
And that means leaving you behind