「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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