「Carboxylic」の共起表現(1語右で並び替え)

「Carboxylic」の共起表現一覧(1語右で並び替え)

Carboxylic

1語右で並び替え

該当件数:162件

to form amides for example, whereas a normal carboxylic acid would just form a salt with an amine.
ctivated acid is to mix NHS with the desired carboxylic acid and a small amount of an organic base i
hyde functional group of an aldose to form a carboxylic acid functional group.
logous to an amide, but the -OH portion of a carboxylic acid is replaced by hydrazine rather than am
onal modification (PTM) process in which the carboxylic acid of the terminal glycine from the di-gly
surface of a protein can have its side chain carboxylic acid deprotonated in environments with pH gr
ups are protected as acetone acetals and the carboxylic acid is in the form of the methyl ester.3
Phloroglucinol carboxylic acid (2,4,6-trihydroxybenzoic acid)
It is the carboxylic acid of piperidine.
This monounsaturated long chain carboxylic acid contains an epoxide.
PFNA is the largest perfluorinated carboxylic acid surfactant.
onanoic acid, an example of a perfluorinated carboxylic acid (PFCA)
They are used to prepare mixed carboxylic acid anhydrides used in peptide synthesis.
The carboxylic acid groups remain available for the conjuga
It is the corresponding carboxylic acid resulting of the hydrolysis of the meth
Reaction with carboxylic acid salts and acid chlorides to the corresp
s formed by esterification - the reaction of carboxylic acid and alcohols.
PFCAs with one carboxylic acid group and five to nine fluorinated carb
e and hemicellulose is degraded to aliphatic carboxylic acid soaps and hemicellulose fragments.
Pivalic acid is a carboxylic acid with a molecular formula of (CH3)3CCO2H
lic acid, is a benzene derivative with three carboxylic acid groups.
It can also be used to label hydroxyl and carboxylic acid functional groups.
The presence of four carboxylic acid functional groups makes possible the bi
Diethylene glycol can be oxidized to the carboxylic acid with strong oxidizing substances like n
acid is an organic compound containing both carboxylic acid and ketone functionality.
By altering the carboxylic acid used, this method is generally able to
However, many esters of this carboxylic acid are stable and these chloroformates are
Oxycinnolin carboxylic acid on heating gives oxycinnoline, melting
Cycloprop-2-ene carboxylic acid is a toxic molecule found in some mushr
es containing a phenolic ring and an organic carboxylic acid function (C6-C1 skeleton).
(+)-cis-2-Aminomethylcyclopropane carboxylic acid ((+)-CAMP) is a GABA agonist selective
noic acid (common name caproic acid), is the carboxylic acid derived from hexane with the general fo
from esterification of paracetamol, and the carboxylic acid Diethylglycin.
rganic compounds that have both hydroxyl and carboxylic acid functional groups.
hippos, horse, ouron, urine) is a carboxylic acid found in the urine of horses and other
skii rearrangement with cyclic ketones where carboxylic acid formation is accompanied by ring-contra
A tricarboxylic acid is an organic carboxylic acid whose chemical structure contains three
ketone group is converted to ring-contracted carboxylic acid 2.5 in a Favorskii rearrangement with p
ring with two adjacent functional groups, a carboxylic acid and an amine.
or pentanoic acid, is a straight-chain alkyl carboxylic acid with the chemical formula C5H10O2.
lidone base structure with 2-oxo-pyrrolidine carboxylic acid (pyroglutamate).
nts from simple esters, fats, triglycerides, carboxylic acid anhydrides, or free fatty acids.
It consists of a piperidine ring with a carboxylic acid moiety in the iso position (and as such
ulinic acid (the alcohol group replaced by a carboxylic acid group), which is biologically more acti
d H2O, whereas its two products are aromatic carboxylic acid and H2O2.
hepatic cytochrome P450 3A4 into its active carboxylic acid metabolite, carebastine.
reparing thiols and activating or protecting carboxylic acid with triphenylphosphine in the followin
-CN) and H2O, whereas its two products are a carboxylic acid (R-COOH) and NH3.
ver, C-3 is not likely to be provided by the carboxylic acid group of tyrosine because tracking of r
to vanillin is achieved by conversion of the carboxylic acid into a thioester with acetyl-CoA.
n with five hydroxyl groups terminating in a carboxylic acid group.
amine pentaacetic acid (DTPA) is a polyamino carboxylic acid consisting of a diethylenetriamine back
activated by enzymatic hydrolysis to several carboxylic acid metabolites, whose urinary excretion ha
ond is subsequently hydrolyzed to generate a carboxylic acid moiety on the remaining substrate fragm
10, and then a decarboxylation to remove the carboxylic acid at C4 provided bartsioside.
laniline with the acid chloride of pyridine- carboxylic acid first gives the 2,6-xylidide of α-picol
al class of organic compounds containing two carboxylic acid groups, such as oxalic acid or succinic
not be confused with gluconic acid, a linear carboxylic acid resulting from the oxidation of a diffe
ng (lactone) by forming an ester between the carboxylic acid group and one of the alcohols.
boxylate reductase, NADPH-L-Delta1-pyrroline carboxylic acid reductase, and L-proline-NAD(P)+ 5-oxid
ith mineral oil by a simple titration of the carboxylic acid moieties present in natural vegetable o
groupd of solketal can be esterified with a carboxylic acid to form the protected monoglyceride, wh
sition is non-glyceride long-chain (C24-C30) carboxylic acid esters (62-68 weight %), free long-chai
nating step despite the observation that its carboxylic acid side chain is stabilized in its carboxy
on binds iron centers very strongly, and the carboxylic acid group by which the ring attaches to var
the first carbon have been fully oxidized to carboxylic acid functions.
nic acids, often molecules containing -COO− ( carboxylic acid) functional groups
anol (an alcohol) reacts with formic acid (a carboxylic acid).
xybenzoic acids (gallic acid, phloroglucinol carboxylic acid).
lene glycol tetraacetic acid) is a polyamino carboxylic acid, a chelating agent that is related to t
Fura-2, a polyamino carboxylic acid, is a ratiometric fluorescent dye which
IUPAC: 3-methylbenzoic acid), is an aromatic carboxylic acid, with formula (CH3)C6H4(COOH).
The iminium intermediate reacts with the carboxylic acid, abstracting an oxide, and regenerating
Unusually for a carboxylic acid, santonic acid does not form hydrogen-b
s oximes, which may be further oxidized to a carboxylic acid, or reduced to form amines.
ion of the 1-hydroxyl group of a ketose to a carboxylic acid, creating an alpha-keto acid.
xylic acid or 3-oxoglutaric acid is a simple carboxylic acid, which may be used as a building block
istry, a diamino acid, also called a diamino carboxylic acid, is a molecule containing at least one
um sulfide it is transformed into athiophene carboxylic acid.
Oxidation of aldehyde group to carboxylic acid.
triacontanoic acid) is a saturated aliphatic carboxylic acid.
susceptible to oxidation to the aldehyde and carboxylic acid.
oic acid (or gheddic acid, geddic acid) is a carboxylic acid.
curonic acid's sixth carbon is oxidized to a carboxylic acid.
acetic acid) is a calcium-specific polyamino carboxylic acid.
, which is further hydrolyzed to a non-toxic carboxylic acid.
d with acetate side arms to form a polyamino carboxylic acid.
in which an hydroxylamine is inserted into a carboxylic acid.
kyl iodide and respectively an alcohol or an carboxylic acid.
tyric acid is not technically a ketone but a carboxylic acid.
ixture of several cyclopentyl and cyclohexyl carboxylic acids with molecular weight of 120 to well o
and branched paraffins, alcohols, aldehydes, carboxylic acids and aromatic compounds.
and branched paraffins, alcohols, aldehydes, carboxylic acids and aromatic compounds.
Reactions with carboxylic acids and their derivatives afford benzimida
Carboxylic acids and phenols also exhibit this effect.
Perfluorinated carboxylic acids (PFCAs), or perfluorocarboxylates are
In general the carboxylic acids of the free diphenols are cyclised to
ldehyde oxidase is an enzyme which generates carboxylic acids from aldehydes.
to convert alcohols into alkyl fluorides and carboxylic acids into acyl fluorides.
They are related to carboxylic acids by replacement of one oxygen centre by
Carboxylic acids (cinnamic, valeric and caproic acid) a
Carboxylic acids react no further than the acyl fluorid
Mesaconic acid is one of several isomeric carboxylic acids obtained from citric acid.
mical compounds which are amides formed from carboxylic acids and ethanolamine.
It converts carboxylic acids into their methyl esters or into their
r fashion 1,1,1-trihalides are hydrolyzed to carboxylic acids in the haloform reaction.
The main fraction are carboxylic acids with a carbon backbone of 9 to 20 carb
is particularly valuable since it works with carboxylic acids which fail to undergo the Schmidt reac
to aziridines and to convert α,β-unsaturated carboxylic acids to α,β-unsaturated bromides.
nthesis is the chemical reaction of aromatic carboxylic acids with metal thiocyanates to form nitril
Haloacetic acids are carboxylic acids in which a halogen atom takes the plac
de by reducing a water dispersion of AQ with carboxylic acids in presence of alkali.
reagent used in organic synthesis to convert carboxylic acids to acyl chlorides.
of peptides by virtue of its reactions with carboxylic acids leading to either the urethane or the
ons expected of an acyl halide: alcohols and carboxylic acids are converted to formate esters and mi
, phosphoric acid can form triesters whereas carboxylic acids only form monoesters. Esterification e
Shortened single bonds are found with carboxylic acids (136 pm) due to partial double bond ch
e used in organic chemistry to form names of carboxylic acids containing the acidic -(C)OOH group.
e of acid catalyst, it converts alcohols and carboxylic acids into the silyl ethers and silyl esters
ulfur, while H2 (in the presence of CO2) and carboxylic acids can be utilized as electron donors.
is used in organic chemistry for converting carboxylic acids to nitriles, for deprotecting acetals
icals include "carbonyl compounds, alcohols, carboxylic acids and their esters, nitrogen- and sulfur
Carboxylic acids can be converted to trifluoromethyl gr
pounds such as certain alcohols, phenols, or carboxylic acids by substituting a trimethylsilyl group
is one of a set of ortho acid derivatives of carboxylic acids that have the general structure of RC(
he preparation of optically active α-hydroxy carboxylic acids, α-hydroxy aldehydes, α-hydroxy ketone
and branched paraffins, alcohols, aldehydes, carboxylic acids, and aromatic compounds.
k cation exchange sorbents contain aliphatic carboxylic acids, which are charged when the pH is abov
Relative to esters of most carboxylic acids, esters of pivalic acid are unusually
ey are amides formed from diethanolamine and carboxylic acids, typically fatty acids.
Like other low-molecular-weight carboxylic acids, it has a very unpleasant odor.
oollins' reagent has been used to selenonate carboxylic acids, alkenes, alkynes, and nitriles.
production of perfluorinated amines, ethers, carboxylic acids, and sulfonic acids.
Like many other carboxylic acids, ceroplastic acid can react with UV cu
midazole is 14.5, making it less acidic than carboxylic acids, phenols, and imides, but slightly mor
Reminiscent of the behaviors of carboxylic acids, DEHPA generally exists as a hydrogen-
ze primary alcohols to aldehydes and then to carboxylic acids, and secondary alcohols to ketones.
yielding the corresponding benzyl ether, and carboxylic acids, yielding the corresponding benzyl est
acids are more acidic than the corresponding carboxylic acids.
e to diazomethane for the methylidenation of carboxylic acids.
ly be oxidised to the aldehyde and not on to carboxylic acids.
r3 is as a catalyst for the α-bromination of carboxylic acids.
the benzyl protecting group for alcohols and carboxylic acids.
here it is used as an activating reagent for carboxylic acids.
om other organic species such as ketones and carboxylic acids.
anhydrides when reacted with sodium salts of carboxylic acids.
n) to create hypohalous acids, aldehydes and carboxylic acids.. Ozone is not as common due to the hi
For carboxylic and sulfonic acids, the products are the cor
te protecting group and for the formation of carboxylic anhydrides.
andem with GC-MS for the analysis of various carboxylic compounds which are ubiquitous in nature.
of hydrolases, specifically those acting on carboxylic ester bonds.
Thus, the two substrates of this enzyme are carboxylic ester and H2O, whereas its two products are
of hydrolases, specifically those acting on carboxylic ester bonds.
carboxylic esterase,
to give elemental hydrogen gas, and reduces carboxylic esters, aldehydes, and ketones to alcohols.
roxy group at a convenient distance from the carboxylic group for the formation of a lactone.
ecause the hydroxy group is too close to the carboxylic group.
Loss of 2 carboxylic groups to tropinone
sses of drugs such as analgesics (morphine), carboxylic nonsteroidal anti-inflammatory drugs (ketopr
Orthocarbonic acid is one of the group of carboxylic ortho acids that have the general structure