「alcohols」の共起表現(1語右で並び替え)

「alcohols」の共起表現一覧(1語右で並び替え)

alcohols

1語右で並び替え

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ls including Alcohol, Amines, Betaines, Fatty alcohols, Acids, Wax, Oils and Petrolatum, Quats, Solv
Three of these alcohols, active amyl alcohol, methyl (n) propyl carbi
ernal olefins, linear and branched paraffins, alcohols, aldehydes, carboxylic acids, and aromatic co
ernal olefins, linear and branched paraffins, alcohols, aldehydes, carboxylic acids and aromatic com
ernal olefins, linear and branched paraffins, alcohols, aldehydes, carboxylic acids and aromatic com
He has worked on the metabolism of aliphatic alcohols, alicyclic hydrocarbons, benzenes and alkylbe
attack from a host of nucleophiles, including alcohols, amines, and enolates with fairly slow rates.
he tosyl group is also a protecting group for alcohols and amines, prepared by combining the alcohol
DCI-11, for alcohols and gasolines containing oxygenates
Alcohols and alkyl halides, diols, thiols
CDI is mainly employed to convert alcohols and amines into carbamates, esters, and ureas
This breaks the fuel down into methane, alcohols, and other lighter-weight fuels.
reported as catalysing the dehydrogenation of alcohols and the reformation of hydrocarbons.
It may also be used to pre-dry some ketones, alcohols, and amines prior to distillation.
The solvent must be aprotic since alcohols and water react with phenylmagnesium bromide
Tellurols are analogues of alcohols and phenols where tellurium replaces oxygen.
lasses: monoterpene hydrocarbons, monoterpene alcohols and straight chain aliphatic alcohols were th
dly in basic or hydroxylic solutions, such as alcohols and amines, to produce thiophosphates.
Long chain aliphatic hydrocarbon alcohols and aldehydes like octanol and octanal are se
is easily opened with nucleophiles including alcohols and water to give polylactones and eventually
troduction of the benzyl protecting group for alcohols and carboxylic acids.
or allow the new protein to act on long chain alcohols and diols, including growth hormones and pher
luble in nonpolar solvents but it reacts with alcohols and water and forms adducts with Lewis bases.
oes the reactions expected of an acyl halide: alcohols and carboxylic acids are converted to formate
at neutral pH, but it is extremely soluble in alcohols and other organic solvents.
ormylation agent for amines, amino acids, and alcohols, and a starting material for formyl fluoride.
e is a powerful catalyst for the acylation of alcohols and phenols, and can be easily recycled and r
hat also cellulose is efficiently degraded by alcohols and strong acid-catalysts at 180°C to 200°C w
reduces esters and acyl chlorides to primary alcohols, and nitriles to primary amines [use Feiser w
boratory is the elimination of alkyl halides, alcohols, and similar compounds.
in the presence of acid catalyst, it converts alcohols and carboxylic acids into the silyl ethers an
t of solution) in comparison with other sugar alcohols, and is very similar to the subtle cooling ef
ter alcoholic extracts, they are: monoterpene alcohols and their glycosides, cyanogenic glycosides,
Alcohols and amines are also commonly used; the hope t
These log-chain isoprenoid alcohols are also called ‘terpenols'.
Hydrocarbons and alcohols are often used as solvents.
The higher sugar alcohols are for the most part nontoxic.
thousands of natural and synthetic compounds, alcohols are diverse and widespread.
Fatty alcohols are mainly used in the production of detergen
Amino alcohols are organic compounds that contain both an am
As a group, sugar alcohols are not as sweet as sucrose, and they have le
Sugar alcohols are not metabolized by oral bacteria, and so
process is not economical as the linear fatty alcohols are more valuable than the corresponding line
that less desirable components (such as fusel alcohols) are returned to the primary flask.
The alcohols are removed from the liquid extract by evapor
Two groups used to protect alcohols are the para-methoxybenzyl and 3,4-dimethoxyb
hosphates, chlorinated hydrocarbons, ketones, alcohols, aromatic hydrocarbons, saturated hydrocarbon
, should be careful not to eat too many sugar alcohols as doing so, with the exception of erythritol
c synthesis to bond one carbonyl group to two alcohols, as in the synthesis of octalactin B. It is p
ations currently label it and all other sugar alcohols at 2.4 kcal/g.
Due to their amphipathic nature, fatty alcohols behave as nonionic surfactants.
ch lower concentration of several other fatty alcohols: behenyl alcohol, lignoceryl alcohol, ceryl a
PEG 400 is soluble in water, acetone, alcohols, benzene, glycerin, glycols, aromatic hydroca
belong as mention in a larger anise-flavored alcohols but certainly they should remain separated as
as a lower laxation threshold than some sugar alcohols, but is more easily tolerated than others suc
on olefins allows the preparation of terminal alcohols by subsequent oxidative cleavage with H2O2 in
portance is the hydrogenolysis of esters into alcohols by catalysts such as copper chromite.
aldehydes and ketones to their corresponding alcohols by utilizing NADH and/or NADPH as cofactors.
These alcohols can be used in "internal combustion engines a
For example, tertiary alcohols cannot be oxidized directly.
ouring chemicals include "carbonyl compounds, alcohols, carboxylic acids and their esters, nitrogen-
ephthalic acid is poorly soluble in water and alcohols, consequently up until around 1970 most crude
Policosanol is a mixture of a few fatty alcohols derived from the waxes of such plants as suga
has been applied whenever the value of fatty alcohols dipped below that of linear olefins because o
Primary alcohols do not work well.
Examples are alcohols, enolates, phenols and enamines.
e more polar than alkenes but not as polar as alcohols, esters, or amides of comparable structure.
acid is a colorless liquid soluble in water, alcohols, ether, benzene, chloroform and other organic
the variance in food energy content of sugar alcohols, EU labeling requirements assign a blanket va
r formulas and structural formulas similar to alcohols, except that sulfur-containing sulfhydryl gro
compounds including sugars, lignans, chitins, alcohols, fats, and aromatic esters, carotenoids and t
acids, fatty acid methyl esters (FAME), fatty alcohols, fatty amines and glycerols are by various ch
diesel fuels can also be produced using other alcohols, for example using ethanol to produce fatty a
is known to reduce certain hydroperoxides to alcohols formed by autoxidation (scheme 1).
It is one of the most common carotenoid alcohols found in nature.
axanthin is one of the most common carotenoid alcohols found in nature.
However, secondary and tertiary alcohols give a substantial amount of alkenes and ethe
halates, adipates, and azelates with C8 - C10 alcohols have found commercial use as lubricants, spin
, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation prod
, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation prod
ple, by addition of ethylene oxide onto fatty alcohols in the presence of suitable catalysts (layer
nd that one can selectively oxidize secondary alcohols in the presence of primary alcohols using NBS
He banned sales and distillation of alcohols in Mongolia in 1297.
ed piv or pv) group is a protective group for alcohols in organic synthesis.
nigs and Knorr treated acetobromoglucose with alcohols in the presence of silver carbonate.
ce and the foam, preventing foam breakdown by alcohols in the burning fuel.
The use of pure alcohols in internal combustion engines is only possib
Moonshine and other homemade alcohols, including two or more of the above mixed tog
sulfate conjugation of primary and secondary alcohols including many hormones, neurotransmitters, d
It is used to convert alcohols into alkyl fluorides and carboxylic acids int
and in the Mitsunobu reaction for converting alcohols into esters.
Like many alcohols, is a water soluble, colourless liquid, but i
etone or ethanol, but dissolution in absolute alcohols is difficult.
of long chain (C36-C46) fatty acids and fatty alcohols joined by an ester bond.
They are similar to alcohols just as silanes are similar to alkanes.
long-chain organic acids (22-26%), long-chain alcohols, ketones, and hydrocarbons (7-15%), and resin
hange the chromatography, these are typically alcohols like methanol, ethanol or isopropyl.
onium also discourages consumption of harmful alcohols like methyl alcohol, and additives like ethyl
Alcohols likewise form alkyl iodides, this providing t
The other amyl alcohols may be obtained synthetically.
from biobutanol and bioethanol, as these are alcohols, not hydrocarbons.
As with other fatty alcohols, octane-1,8-diol is used in cosmetics as an e
ood oil contains more than 90% sesquiterpenic alcohols of which 50-60% is the tricyclic α-Santalol.
production of a significant quantity of fusel alcohols, or spoilage of the finished beer by other or
ters formed from other pentanol isomers (amyl alcohols), or mixtures of pentanols, are often referre
This follows a process where no alcohols, or animals fats are used in the manufacturin
When warmed with alcohols, or on prolonged boiling with other solvents,
ethyl acetate, chloroform, benzene and lower alcohols or ketones.
On producing wells, injection of chemicals or alcohols or oil distillates to prevent and or solve pr
ine-copolymere, as source for synthetic fatty alcohols or olefine sulfonates.
ed, usually with sulfur dioxide but also with alcohols or formaldehyde, in the presence of sulfuric
en peroxide, antiseptics, ketones, as well as alcohols other than ethanol (drinking alcohol) such as
oxidant is useful for the dehydrogenation of alcohols, phenols and steroid ketones in organic chemi
rather non-volatile compounds such as certain alcohols, phenols, or carboxylic acids by substituting
ncentration of high boiling compounds such as alcohols, polyethylene glycols, diols, phenols, monoam
chloride, plasticizers, specialty additives, alcohols, polyolefins, acrylic acids, rubbers, styreni
Common: Blended with other alcohols produced from molasses or mixed with neutral
h it is not refined to separate the different alcohols produced by fermentation and exhaustion.
se D that allows the creation of phosphatidyl alcohols rather than phosphatidic acid in the presence
ent in some berries, and other polyols (sugar alcohols), such as erythritol, mannitol, and other ing
e, glucose, galactose and maltose, as well as alcohols such as glycerol, inositol and mannitol.
The angelic acid esters of sesquiterpene alcohols, such as petasin, are the active chemical beh
They are amino alcohols that are derivatives of 1-amino-2-propanol.
he body had no mechanism for catabolizing the alcohols, they would build up in the body and become t
Conversion of primary alcohols to carbamates.
Reaction with alcohols to form carbonates
It also reacts with alcohols to give methyl ethers, where diazomethane may
donor could react with simple or carbohydrate alcohols to establish the glycosidic linkages.
xide catalyzes dehydration of acyclic primary alcohols to aldehydes and ketones.
organic synthesis: they will oxidize primary alcohols to aldehydes and then to carboxylic acids, an
The reagent is mostly used to convert primary alcohols to alkyl fluorides under mild conditions with
rangement, a Claisen rearrangement of allylic alcohols to give allylic trichloroacetamides.
DAST converts alcohols to the corresponding alkyl fluorides as well
Oxidation - The conversion of alcohols to ketones or aldehydes can be effected by me
plastic acid can react with UV curable moiety alcohols to form reactive esters, such as 2-allyloxyet
m can be used to oxidize primary or secondary alcohols to the corresponding aldehydes and ketones.
Dehydration of alcohols to linear alpha olefins by passing alcohols i
to produce different substances, ranging from alcohols to alkoxide salts.
c reaction that is based on the activation of alcohols towards nucleophilic attack.
Reaction temperatures are milder as well - alcohols typically react at -78 °C and ketones around
Sharpless epoxidation of allyl alcohols using titanium isopropoxide, diethyl tartrate
h Vieux unique - they include fusel oil, amyl alcohols, vanillin, esters, 'blokdrop' (which may tran
A number of primary and secondary alcohols was tested, from methanol to 2-butanol.
with air, halogens, halogenated hydrocarbons, alcohols, water, and any substance which possesses an
The most important reaction of PBr3 is with alcohols, where it replaces an OH group with a bromine
Primary alcohols will only be oxidised to the aldehyde and not
Reactions with alcohols will result in the formation of esters and re
As with other sugar alcohols, with the exception of erythritol, consumptio
application of dimethoxymethane is to protect alcohols with a MOM ether in organic synthesis.
opposed These are two completely different alcohols with different cultures behind them as such t
solutions containing either isolefin or tert alcohols with this reagent will result in the formatio
developed in order to drink highly rectified alcohols without the burning sensation.
troduction of the benzyl protecting group for alcohols, yielding the corresponding benzyl ether, and