「PYRIDINE」の共起表現(1語右で並び替え) - Weblio英語共起表現検索


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Weblio 辞書 > 英和辞典・和英辞典 > PYRIDINEの意味・解説 > PYRIDINEに関連した共起表現

「PYRIDINE」の共起表現一覧(1語右で並び替え)

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


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