「NUCLEOPHILE」の共起表現(1語右で並び替え)

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共起表現

「NUCLEOPHILE」の共起表現一覧(1語右で並び替え)

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Trimethylamine is a good	nucleophile, and this reaction is the basis of most of
The anion is a	nucleophile, and most electrophiles react with it by ad
PhSeNa is a useful	nucleophile, and can be used to introduce the phenylsel
p catalytic triad with serine acting as the	nucleophile and gly-met providing stabilization of the
Phenylmagnesium bromide is a strong	nucleophile as well as a strong base.
Methylamine is a good	nucleophile as it is highly basic and unhindered, altho
an alcohol, but a tertiary carbon with the	nucleophile as a substituent.
As a consequence, thiocyanate can act as a	nucleophile at either sulfur or nitrogen - it is an amb
The amino	nucleophile attacks the carbon
f α-D-galactose, and the resulting alkoxide	nucleophile attacks the γ-phosphorus of ATP.
equipped to be the source of the hydroxide	nucleophile because of its proximity to the scissile ph
Instead, Glu-537 is the actual	nucleophile, binding to a galactosyl intermediate.
law is deceptive: hydroxide serves not as a	nucleophile but as a base to deprotonate the coordinate
The	nucleophile can be carbon, nitrogen or oxygen based.
conserved histidine (His80) that acts as a	nucleophile during catalysis.
A	nucleophile favors addition from the "inside" of the en
It is also a	nucleophile for the production of methyl ethers.
t the branch adenosine specifying it as the	nucleophile for the first transesterification.
e is required for in-situ generation of the	nucleophile from a precursor.
In the reaction product the	nucleophile has replaced the leaving group. .
In E. coli, Glu-461 was thought to be the	nucleophile in the substitution reaction.
own-6, potassium acetate is a more powerful	nucleophile in organic solvents.
lfonamide 1 or its deprotonated form 2 is a	nucleophile in reaction with the aldehyde 3 to intermed
ontrol an electron donor molecule acts as a	nucleophile, in kinetic reaction control the electron d
When the	nucleophile is an hydride the reaction is called conjug
s, cyanide, which is classified as a strong	nucleophile, is used to prepare nitriles, which occur w
studies on the role of Cys48 as a possible	nucleophile, it has not been determined if nucleophilic
leavage in the presence of (an excess of) a	nucleophile like phloroglucinol (reaction called phloro
962 published on the reaction of water as a	nucleophile on olefin-palladium chloride complexes to f
alkyl bond begins with attack of the alkyl	nucleophile on the sulfur centre in SO2.
In these reactions, the incoming	nucleophile replaces the NR2 moiety.
e oxide) ring opening and activation of the	nucleophile, ring, or combination thereof via the catal
orobenze has a chloro group replaced with a	nucleophile such as the hydroxide mentioned forming the
Note that nitrogen is a better	nucleophile than oxygen and most nitrites would react v
It is a powerful	nucleophile that can be used to prepare methylthioether
ing between Asn68 and Asn212, activates the	nucleophile that attacks and cleaves the phosphodiester
lecules strongly depends upon the nature of	nucleophile, the type of leaving group, site of displac
f GALT, the His166 residue acts as a potent	nucleophile to facilitate transfer of a nucleotide betw
d in the substrate, whereas Asp52 acts as a	nucleophile to generate a glycosyl enzyme intermediate.
ion is the combination of a carbon-centered	nucleophile with an electrophilic source of fluorine to
ladium catalysed substitution reaction of a	nucleophile with a substrate containing a leaving group
The TPP can then act as a	nucleophile with the loss of this C2 hydrogen, forming

共起表現

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「NUCLEOPHILE」の共起表現一覧(1語右で並び替え)