「PYRIDINE」の共起表現(2語左で並び替え)

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共起表現

「PYRIDINE」の共起表現一覧(2語左で並び替え)

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Davicil is a chlorinated	pyridine derivative with antimicrobial properties, whi
(C-terminal) has the topology of a classical	pyridine dinucleotide-binding fold (i.e. a central par
kyne 1,5-hexadiyne with copper(II) acetate in	pyridine to give the trimer, followed by deprotonation
This enzyme is also called	pyridine methyltransferase.
The direct amination of	pyridine with sodium amide takes place in liquid ammon
siccant for basic solvents such as amines and	pyridine.
e prepared by oxidation of tertiary amines or	pyridine analogs with hydrogen peroxide (H2O2), Caro's
ved in dichloromethane with a small amount of	pyridine.
gh phosphorine is a heavier element analog of	pyridine, the electronic structure is very different f
on-donors such as tetrathiafulvalene and even	pyridine to give mixed valence charge-transfer salts.
ietary composition of iodine and poly-2-vinyl	pyridine, neither of which is electrically conductive,
one pair of electrons on the nitrogen atom of	pyridine is not delocalized, and thus pyridine can be
Dihydropyridine is a molecule based upon	pyridine, and the parent of a class of molecules that
Arsabenzene is far less basic than	pyridine, being unreactive with Lewis acids.
ole approximately sixty times more basic than	pyridine.
evelopment of direct arylation of benzene and	pyridine N-oxide.
O bond in carbon monoxide and the C-N bond in	pyridine.
y reacting THC with phosphoryl chloride using	pyridine as a solvent, following by quenching with wat
,6-dimethylaniline with the acid chloride of	pyridine- carboxylic acid first gives the 2,6-xylidide
ving group by reaction with mesyl chloride in	pyridine which enables the third ring closure to 15.
It may also be obtained as a co-product of	pyridine synthesis from acetaldehyde, formaldehyde, an
roketolide, solithromycin, do not contain the	pyridine moiety and do not antagonize these cholinergi
Structure of the complex of CrO5 with	pyridine
practice the chromium byproduct deposits with	pyridine as a sticky black tar, which can complicate m
It is a dimethyl substituted derivative of	pyridine.
It is formally derived from	pyridine by substitution of the 3 and 4 positions with
thesized, with good yields by displacement of	pyridine ligands of the trispyridine complex Mo(CO)3(p
In enzymology, a	pyridine N-methyltransferase (EC 2.1.1.87)
This gene encodes a member of the family of	pyridine nucleotide oxidoreductases.
Pyridinium refers to the cationic form of	pyridine.
and a molecule of cyclopentadiene to form the	pyridine ring.
iracetam, but differs mostly in that it has a	pyridine ring in place of aniracetam's benzene ring.
In 1868 he discovered	pyridine and related organic compounds such as picolin
When heated with	pyridine to 140 °C, it is converted into allommic acid
loroanthraquinone with anhydrous hydrazine in	pyridine at 100 °C.
perester 2.6 (with t-butyl hydroperoxide and	pyridine) to 2.7; afterward, the acetal is once more r
Clopyralid is in the	pyridine family of herbicides, which also includes pic
The positions in the	pyridine system attacked by the electrophiles are the
e, it may be prepared by reacting iodine with	pyridine in the presence of silver tetrafluoroborate s
The second way is from	pyridine, which undergoes alkylation by 4-chlorobenzyl
Picolinic acid is a	pyridine compound with a carboxyl side chain at the 2-
Actinidine is a	pyridine derivative found in the essential oil of vale
extrusion of sulfur, and the endproduct is a	pyridine; in one study, a very mild reaction of a 2-(d
of this enzyme are S-adenosyl methionine and	pyridine, whereas its two products are S-adenosylhomoc
t of DHA in dichloromethane with a mixture of	pyridine, a catalytic amount of DMAP and succinic anhy
It is notable for its concentrations of two	pyridine alkaloids: lobeline and nicotine.
This means .0095% of the	pyridine is in the protonated form of C5H6N+.
is a antihistamine and anticholinergic of the	pyridine chemical class which was developed in the ear
ction, only electrophilic substitution on the	pyridine ring was possible, which is difficult because
eaction is a nucleophilic substitution on the	pyridine ring; the 2nd and 6th positions are therefore
The oxidation of	pyridine is effected with peracetic acid, a reaction t
opic solid is the product of the oxidation of	pyridine.
Examples of amine oxides include	pyridine N-oxide, a water-soluble crystalline solid wi
The lone pair of	pyridine is its HOMO, so pyridine has good σ-donating
with a 0.55 positive charge on phosphorus and	pyridine with a -0.67 negative charge on nitrogen also
then reacted with ethyl piperazinoacetate and	pyridine.
Examples of basic aromatic rings are	pyridine or quinoline.
xazole ring structure, and an odor similar to	pyridine.
hloride, usually in an aprotic solvent, often	pyridine, the basicity of which activates the reaction
e is reduced by nitrogen heterocycles such as	pyridine.
e conducted in the presence of a base such as	pyridine that absorbs the hydrogen chloride.
acid and can react with a Lewis base, such as	pyridine in a non-aqueous medium such as dichlorometha
large excess of a coordinating amine such as	pyridine which presumably binds to lead in the course
other nitrogen heterocylic compounds, such as	pyridine derivatives, quinoline is often reported as a
Sulfur trioxide	pyridine complex is a complex formed where the lone pa
They are efficiently synthesized from	pyridine sulfonate.
The study showed that a	pyridine moiety that is part of the telithromycin mole
component reaction is related to the Hantzsch	pyridine synthesis.
novel terpyridine synthesis, the Chichibabin	pyridine synthesis.
Then the aromatic	pyridine ring is reduced to piperidine by hydrogen in
homebake” process involves use of the reagent	pyridine hydrochloride to convert the codeine to morph
THF or	pyridine) through hydrogen bonding.
triazines can be reacted with alkynes to form	pyridine rings.
ne or an aldehyde using chromium trioxide and	pyridine.
Other names in common use include	pyridine nucleotide transhydrogenase, transhydrogenase
Other names in common use include	pyridine nucleotide transhydrogenase, transhydrogenase
Not to be confused with Chichibabin	pyridine synthesis.

共起表現

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「PYRIDINE」の共起表現一覧(2語左で並び替え)