「Esters」の共起表現一覧(1語右で並び替え)
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bers also serve as major receptors for phorbol | esters, a class of tumor promoters. |
the formation of one or sometimes two sulfate | esters, adenosine 5'-phosphosulfate (APS) and 3'-phos |
ompounds is also sometimes known as Tammelin's | esters, after Lars-Erik Tammelin of the Swedish Insti |
elemental hydrogen gas, and reduces carboxylic | esters, aldehydes, and ketones to alcohols. |
Aldehydes and formic acid (and formic acid | esters) also give a positive test. |
MWPE does not contain chemical groups (such as | esters, amides or hydroxylic groups) that are suscept |
Seeds contain tetranorterpenes, phragmalin | esters and 12 α-OAc-phyramalin (Asolkar et al.., 1992 |
with alcohols will result in the formation of | esters and reactions with amines will generate amides |
They produce a stomach oil made up of wax | esters and triglycerides that is stored in the proven |
ced in the body from the hydrolysis of retinyl | esters, and from the reduction of retinal. |
lly, they produce a stomach oil made up of wax | esters and triglycerides that is stored in the proven |
in the synthesis of glycerol, glycidyl ethers, | esters and amines. |
re also known as organocarbonates or carbonate | esters, and have the general formula ROCOOR′, or RR′C |
Acetic acid is used in VAM, PTA | esters and other intermediates and acetic anhydride i |
nesulfonyl chloride, CH3C6H4SO2Cl, which forms | esters and amides of toluenesulfonic or tosylic acid. |
and carboxylic acids are converted to formate | esters and mixed acid anhydrides, respectively. |
By contrast, LiAlH4 reduces | esters and acyl chlorides to primary alcohols, and ni |
domain in Protein Kinase C (that bind phorbol | esters and diacylglycerol) (see PDOC00379) and the pr |
lammatory cytokines, peptide hormones, phorbol | esters, and neurotransmitters" and physical stimuli i |
ree long-chain fatty acids into fatty acyl-CoA | esters, and thereby play a key role in lipid biosynth |
DAG), structured triacylglycerols (TAG), sugar | esters and other oleochemical products. |
t; acetaldehyde and its aldol products; higher | esters; and ketones. |
Similar to sterol | esters and stanol esters, stigmasterol inhibits the a |
Esters and salts of glutaconic acid are called glutac | |
rp.) for "Solvents for Gums, Resins, Cellulose | Esters, and the Like", ; the first one was ethyl cell |
Montanic acid ethylene glycol | esters and glycerol esters are used as protective lay |
o convert alcohols and amines into carbamates, | esters, and ureas. |
This reduces fruity | esters and gives the beer a cleaner flavor. |
possible to form new C-C bonds, rings, amides, | esters, and acids. |
Its | esters are known for their resistance to heat, light, |
Esters are organic compounds formed by esterification | |
Typically phthalate | esters are prepared from the widely available phthali |
Short chain | esters are used as high-boiling, biodegradable, low-t |
Sorbitan | esters are also used as emulsifiers and stabilisers i |
Fully hydrogenated jojoba | esters are most often small beads used to exfoliate t |
Jojoba | esters are the hydrogenation or interesterification p |
In general, α-halocarboxylic acids and their | esters are good alkylating agents and should be handl |
The salts and | esters are relatively uncommon, and their uses appear |
Haus Lange and Haus | Esters are residential houses designed by Ludwig Mies |
Esters are chemical compounds derived by reacting an | |
It and its | esters are used in preparing perfumes to imitate jasm |
Bisphenol-A and novolac based cyanate | esters are the major products, bisphenol-F and bisphe |
Bischoline | esters are compounds that can act as a competitive ag |
Mixtures of different methyl dibasic | esters are commercially produced from short-chain aci |
Dibasic | esters are used in paints, paint strippers, coatings, |
Halogen-free pentaerythritol | esters are also environmentally friendly alternative |
esins based on acrylic and/or methacrylic acid | esters are invariably produced by radical polymerizat |
Phosphite | esters are used in the Perkow reaction in the formati |
Jojoba | esters are very resistant to oxidation, more so than |
Physically, jojoba | esters are an odourless, colourless liquid, white cre |
Chemically, jojoba | esters are a complex mixture of long chain (C36-C46) |
Mesylate | esters are a group of organic compounds that share a |
Long-chain acyl-CoA | esters are substrates for a number of important enzym |
The precursors to such | esters are alcohols. |
Phenylsulfinic acid and its | esters are chiral. |
Salts and | esters are known as thiomalates. |
Interesterified Jojoba | Esters are commonly used in cosmetic formulations as |
TFP | esters are stable for several hours at the basic pH, |
Jojoba | esters are proper waxes; there is no triglyceride com |
Cyanate | esters are chemical substances generally based on a b |
Wax | esters are also found in some plants, notably jojoba. |
Sterol | esters are added to certain Unilever products under t |
Phosphomonoesters (or phosphoric | esters) are chemical compounds containing one ester b |
Polyaspartic | esters are a new type of amine functional coreactant |
Monothiophosphate | esters are biochemical reagents used in the study tra |
Also, a variety of polymerizable | esters are prepared from allyl alcohol, e.g. |
Unlike the acetate salts, acetate | esters are often liquids, lipophilic, and sometimes v |
Maleic acid | esters are also called maleates, for instance dimethy |
entually, the advantages of using polyaspartic | esters as the main component of the co-reactant for r |
Epoxy-based vinyl | esters benefits |
sed in the manufacture of acrylic acid and its | esters, but its use has been mostly phased out in fav |
m kernel or coconut oil fatty acids and methyl | esters by reduction. |
The number of | esters can be up to ten as in oligo-(R)-3-hydroxybuty |
Phosphite | esters can be prepared by reacting phosphorus trichlo |
The rate of reaction of Polyaspartic | esters can be manipulated, thus extending the pot-lif |
Cyanate | esters can also be mixed with bismaleimides to form B |
Cyanate | esters can be cured and postcured by heating, either |
Phorbol | esters can directly stimulate PKC. |
Phosphite | esters can be considered as esters of phosphorous aci |
Glycidic | esters can also be obtained via nucleophilic epoxidat |
Phorbol | esters can directly stimulate protein kinase C, PKC. |
Stanol | esters can also be used in low-fat foods. |
lignans, chitins, alcohols, fats, and aromatic | esters, carotenoids and terpenes. |
Tetrafluorophenyl (TFP) | esters chemistry typically used to attach fluorophore |
Pentafluorophenyl (PFP) | esters chemistry typically used to attach fluorophore |
e, bromine, iodine, hypochlorite salts, osmate | esters, chromium trioxide and potassium permanganate. |
) engines that is made of fatty acid monoalkyl | esters derived from biologically produced oils or fat |
Esters derived from HFBA readily undergo condensation | |
ial chemical widely used for preparing acetate | esters, e.g. |
mending Schedules I and II to include isomers, | esters, ethers, salts of isomers, esters and ethers, |
iphenylphosphine) and assists the synthesis of | esters, ethers, amines and thioethers of alcohols. |
As with many volatile | esters, ethyl benzoate has a pleasant odor which coul |
lsifiers or lipophilic surfactants from simple | esters, fats, triglycerides, carboxylic acid anhydrid |
nic acid; erucyl alcohol; behenyl alcohol; wax | esters; fatty acids; brassylic acid and pelargonic ac |
ing material useful for making Pinacol boronic | esters for organic synthesis. |
manufacturing of the methyl, ethyl, and benzyl | esters for the perfume industry. |
However, | esters formed from other pentanol isomers (amyl alcoh |
hydroxyl groups were protected with as acetate | esters, forming structure 10. |
ate is a useful reagent for preparing xanthate | esters from alkyl and aryl halides. |
by Walter Reppe for the synthesis of acrylate | esters from alkynes, carbon monoxide, and alcohols. |
hetic chemistries, including polyalphaolefins, | esters, glycols, polyphenylethers, silicones, alkylat |
Some | esters have use as muscle relaxants, while others are |
Sterol | esters have been shown to reduce the level of low-den |
Cholesteryl | Esters have a lower solubility in water than Choleste |
ngent cheesy or sweaty smell, but its volatile | esters have pleasing scents and are used widely in pe |
Acetate | esters have the general formula CH3CO2R, where R is a |
mple using ethanol to produce fatty acid ethyl | esters, however these types of biodiesel are not cove |
2002, Fischl collaborated with the Museum Haus | Esters in Krefeld, Germany. |
Octanol occurs naturally in the form of | esters in some essential oils. |
sumed that plant pectinesterases remove methyl | esters in a progressive block-wise fashion, giving ri |
sferase catalyzes the formation of cholesterol | esters in lipoproteins. |
Important chloroformate | esters include 4-nitrophenyl chloroformate, fluorenyl |
For the class of hydroxybenzoate | esters, including discussion on possible health effec |
For this reason, polyaspartic | esters initially found use in conventional solvent-bo |
commercial importance is the hydrogenolysis of | esters into alcohols by catalysts such as copper chro |
the -yl organic chemical naming convention for | esters, is also frequently seen. |
Haus | Esters is a 1928 home, designed by Mies van der Rohe |
precursor of derivative | esters; isobutyl esters such as diisobutyl phthalate |
Like many | esters it has a fruity or floral smell at low concent |
most worker friendly of the aviation phosphate | esters; it is least irritating to skin and less prone |
As is the case with most volatile | esters, it has a pleasant aroma and taste. |
f carbonyl-containing functionalities (such as | esters, ketones, amides, aldehydes, etc.). |
Museum Haus | Esters, Krefeld, Germany 2007 |
evel,High free cholesterol and low cholesterol | esters levels. |
cetate has three isomers that are also acetate | esters: n-butyl acetate, isobutyl acetate, and tert-b |
tion of the RhoGAP activity of CHN1 by phorbol | esters, natural compounds mimic of the lipid second m |
ompounds, alcohols, carboxylic acids and their | esters, nitrogen- and sulfur-containing compounds, ta |
Gluconic acid, gluconate salts, and gluconate | esters occur widely in nature because such species ar |
The salts and | esters of apocholic acid are known as apocholates. |
The salts and | esters of this acid are known as hexanoates or caproa |
es are a class of chemical compounds which are | esters of chloroformic acid. |
Various | esters of nonanol, such as nonyl acetate, are used in |
so common in consumer products are the sulfate | esters of ethoxylated fatty alcohols. |
The carboxylate anion and the | esters of hydroxybutyric acids are known as hydroxybu |
All these compounds are tyrosol | esters of elenolic acid that are further hydroxylated |
Polymers derived from pivalate | esters of vinyl alcohol are highly reflective lacquer |
The retinyl | esters of the RPE are chaperoned by a protein known a |
It is made up primarily of | esters of lauric, myristic, and palmitic acid. |
trimonium chloride or cocamidopropyl betaine), | esters of phosphoric acid, polyethylene glycol esters |
However, many | esters of this carboxylic acid are stable and these c |
Volatile | esters of 2-butanol have pleasant aromas and are used |
Cyclic | esters of hypomanganic acid are thought to be interme |
An organophosphate is the general name for | esters of phosphoric acid and is one of the organopho |
Volatile | esters of valeric acid tend to have pleasant odors an |
rbitan tristearate is a mixture of the partial | esters of sorbitol and its anhydrides with stearic ac |
iacylglycerides (in addition to phospholipids, | esters of cholesterol, and lipid soluble vitamins). |
Examples of gallotannins are the gallic acid | esters of glucose in tannic acid (C76H52O46), found i |
it is abbreviated as TsO−, or it may refer to | esters of p-toluenesulfonic acid. |
ithin, guar gum, natural flavors, polyglycerol | esters of fatty acids, sorbitan monostearate. |
in stable organic compounds; they are formally | esters of orthocarbonic acid, and therefore are calle |
Dibasic | esters of phthalates, adipates, and azelates with C8 |
The angelic acid | esters of sesquiterpene alcohols, such as petasin, ar |
ical compounds consisting of various isoheptyl | esters of phthalic acid with the chemical formula C22 |
ganic chemistry, sultones are cyclic sulfonate | esters of hydroxy sulfonic acids that exist mainly as |
Various | esters of phorbol have important biological propertie |
The reverse | esters of many drugs which contain an ester group in |
ase of citric acid, (C3H5O(COO)33−), or to the | esters of citric acid. |
to synthesize dioxindoles 3 from anilines and | esters of mesoxalic acid 1. |
Esters of propane-1,2,3-tricarboxylic acid are found | |
They are | esters of phosphinous acid. |
ic components, such as fatty acid anilides and | esters of PAP, have provided evidence that these mark |
Roman chamomile, in which | esters of angelic and tiglic acids are the principal |
of organophosphate compounds (organophosphate | esters of substituted aminoethanethiols). |
Long chain | esters of adipic acid are used as lubricants for the |
F-fucoidan, which is >95% composed of sulfated | esters of fucose, and U-fucoidan, which is approximat |
Relative to | esters of most carboxylic acids, esters of pivalic ac |
sists of approximately 95% of a mixture of the | esters of sorbitol and its mono- and dianhydrides. |
Formally they are alkyl | esters of nitrous acid. |
investigating the potential of organophosphate | esters of substituted aminoethanethiols for use as pe |
Decanoate salts and | esters of various drugs are available. |
Salts and | esters of decanoic acid are called decanoates. |
Salts and | esters of methanesulfonic acid are known as mesylates |
Xanthates also refer to | esters of xanthic acid. |
Esters of azelaic acid find applications in lubricati | |
They are | esters of phosphoric acid H3PO4 and corresponding alc |
are medium-chain (6 to 12 carbons) fatty acid | esters of glycerol. |
The | esters of thiocyanic acid have the general structure |
The salts and | esters of thiocyanic acid are known as thiocyanates. |
Salts and | esters of the acid are called butyrates or butanoates |
en to nonafluorobutanesulfonates, the salts or | esters of perfluorobutanesulfonic acid. |
organic compounds belonging to the classes of | esters or ethers. |
It converts carboxylic acids into their methyl | esters or into their homologues (see Arndt-Eistert sy |
lar than alkenes but not as polar as alcohols, | esters, or amides of comparable structure. |
cellulose, ETN, or any number of soluble nitro | esters or gelling agents. |
al formulation they are given as the palmitate | esters, or formulated in capsules. |
rivatives of trifluoroacetic acid, such as the | esters or acid chloride. |
by hydrolysis of phenolic | esters or ethers |
Sterol | esters, or sterids are a heterogeneous group of chemi |
getable oil and alcohol are reacted, producing | esters, or biodiesel, and the coproduct, glycerol. |
limits of 0-25 mg of polyoxyethylene sorbitan | esters per kg body weight. |
Polyaspartic | esters perform well as a reactive diluting agent for |
Today, synthetic hydrocarbons, | esters, polyglycols, silicones. |
fficiently that some fatty acids, proteins and | esters precipitate out so that they are caught on the |
odour, which is partly imparted by the acetyl | esters present in generous amounts. |
DMHP and its | esters produce sedation and mild hallucinogenic effec |
nversion of these acids to their corresponding | esters produces some of the volatile components of he |
Like most | esters, propyl propanoate has a distinctly fruity odo |
The different testosterone | esters provide for different half lives. |
near-quantitative yields of the desired methyl | esters, RCO2Me. |
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