「Ketone」の共起表現一覧(1語右で並び替え)
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| Methyl vinyl | ketone, acetoacetic ester, and diethyl-methyl-(3-oxo- |
| obemidone is so named because it is the propyl | ketone analogue of bemidone (hydroxypethidine). |
| Methyl vinyl | ketone and acetoacetic ester undergo aldol cyclizatio |
| intained so long as the positions of the aryl, | ketone and pyrrolidinyl groups are held constant, whi |
| en further oxidized and esterified to form the | ketone and acetate ester moieties seen in forskolin. |
| s a phenoxyacetic acid derivative containing a | ketone and a methylene group. |
| d by Georges Darzens in 1904 from methyl nonyl | ketone and ethyl chloroacetate. |
| triphenylphosphine closes the ring between the | ketone and the azide to the tetrahydropyridine 12. |
| l)-acetic acid hydrazide with reduction of the | ketone at the 3-position. |
| It is a hydroxy | ketone attached to two phenyl groups. |
| The brain, in particular, relies heavily on | ketone bodies as a substrate for lipid synthesis and |
| In the | ketone bodies digestion pathway (in the tissue), it i |
| Other | ketone bodies such as beta-ketopentanoate and beta-hy |
| When | ketone bodies are measured by way of urine concentrat |
| Ketone bodies are relevant to neurological diseases s | |
| yl-CoA is then used instead in biosynthesis of | ketone bodies via acetoacyl-CoA and β-hydroxy-β-methy |
| he strip changes color indicating the level of | ketone bodies detected, which reflects the degree of |
| Ketone bodies | |
| The three endogenous | ketone bodies are acetone, acetoacetic acid, and beta |
| Ketone bodies are produced mainly in the mitochondria | |
| Like the other | ketone bodies (acetoacetate and acetone), levels of b |
| It also takes a similar role in the | ketone bodies synthesis pathway of the liver. |
| The | ketone bodies produced in the liver can also cross th |
| e participates in synthesis and degradation of | ketone bodies and butanoate metabolism. |
| usable energy, is the source of the two other | ketone bodies below |
| The production of | ketone bodies is then initiated to make available ene |
| In the brain, these | ketone bodies are then incorporated into acetyl-CoA a |
| id is an amino acid that can be converted into | ketone bodies through ketogenesis. |
| The popular dipstick used to detect | ketone bodies in urine "Ketostix" by Bayer, only dete |
| mobilisation of glucose, free fatty acids and | ketone bodies, which are metabolites produced in exce |
| acid metabolism, synthesis and degradation of | ketone bodies, valine, leucine and isoleucine degrada |
| Besides its role in the synthesis of | ketone bodies, HMG-CoA is also an intermediate in the |
| As opposed to 4-carbon | ketone bodies, beta-ketopentanoate is anaplerotic, me |
| mitochondria of liver and kidney cells to the | ketone bodies- acetoacetate, beta-hydroxybutyrate, an |
| etogenic amino acids, which are converted into | ketone bodies. |
| vels of acetone much lower than those of other | ketone bodies. |
| rom fats and lipids are transformed into three | ketone bodies: acetone, acetoacetate, and D-β-hydroxy |
| Chemical structures of the three | ketone bodies: acetone (top), acetoacetic acid (middl |
| cycle stalling and shifting of glucose towards | ketone body production |
| The | ketone body acetoacetate will slowly decarboxylate in |
| nverted to glucose as both carbon atoms in the | ketone body are ultimately degraded to carbon dioxide |
| A transferase deficiency is an inborn error of | ketone body utilization. |
| In alcoholic ketoacidosis, this | ketone body is produced in greatest concentration. |
| nts glucose absorption and can cause unchecked | ketone body production (through fatty acid metabolism |
| Acetoacetate is a | ketone body, which is activated with succinyl-CoA, an |
| hydroxybutyrate or 3-hydroxybutyric acid) is a | ketone body. |
| opanol, acetone, acetic acid, and methyl ethyl | ketone, but insoluble in benzene, carbon tetrachlorid |
| The thioketal prepared from the | ketone can be easily reduced by catalytic hydrogenati |
| azing in fields in which it grows, the perilla | ketone causes pulmonary edema leading to a condition |
| four kinds of organic compounds: (i) a methyl | ketone: CH3COR, acetaldehyde (CH3CHO), ethanol (CH3CH |
| ohydrin, beta-glucosyltransferase, UDP glucose | ketone cyanohydrin glucosyltransferase, UDP-glucose:k |
| It is a | ketone derivative of tetralin. |
| s multifunctional: it exhibits properties of a | ketone, forming an oxime; an oxidant, forming the dih |
| will cleave vicinal diols into two aldehyde or | ketone fragments. |
| fferentiate between water-soluble aldehyde and | ketone functional groups, and as a test for monosacch |
| Butyrophenone is a chemical compound (with a | ketone functional group); some of its derivatives (ca |
| containing five carbon atoms, and including a | ketone functional group. |
| iones are a derivatives of piperidine with two | ketone functional groups. |
| containing five carbon atoms, and including a | ketone functional group. |
| membered ring containing one oxygen atom and a | ketone functional group. |
| a monosaccharide with seven carbon atoms and a | ketone functional group. |
| tional group in position 1 (aldotetroses) or a | ketone functional group in position 2 (ketotetroses). |
| tional group in position 1 (aldoheptoses) or a | ketone functional group in position 2 (ketoheptoses). |
| ting of a cyclopropane carbon framework with a | ketone functional group. |
| c compound containing both carboxylic acid and | ketone functionality. |
| yde group is C1; in a ketose the carbon of the | ketone group has the lowest possible number (usually |
| The newly formed | ketone group then forms another C-C bond by photochem |
| The | ketone group is then reduced by means of zinc and amm |
| If the sugar contains a | ketone group, it is a ketose and if it contains an al |
| f chemical structure only by the addition of a | ketone group, to the azepine ring, and is approximate |
| Hydroxyquinones with hydroxyls adjacent to the | ketone groups often exhibit intramolecular hydrogen b |
| l groups adjacent to the double bond and three | ketone groups on the remaining carbon atoms. |
| The polar | ketone groups in the polymer backbone of these materi |
| ation with palladium on carbon and that of the | ketone groups to alcohol groups in 15 by sodium boroh |
| 2.2 includes enzymes that transfer aldehyde or | ketone groups |
| A diketone is a molecule containing two | ketone groups. |
| h the replacement of two hydrogen atoms by two | ketone groups. |
| In organic chemistry | ketone halogenation is a special type of halogenation |
| Similar chemistry yielded the six-fold | ketone hexaoxotricyclobutabenzene C12O6, which happen |
| It has a terminal aldehyde group rather than a | ketone in its linear chain, and so is considered part |
| sample is added to a 1% solution of Mischler's | ketone in benzene or toluene. |
| PEP in that the alpha carbon is extended and a | ketone is attached to the beta carbon (with the excep |
| eakdown to hydrogen cyanide and an aldehyde or | ketone is catalyzed by a hydroxynitrile lyase (abbrev |
| Valerophenone, or butyl phenyl | ketone, is an aromatic ketone. |
| If an α-halo | ketone is used, the product is an α,β-epoxy ketone. |
| Perilla | ketone is a natural terpenoid that consists of a fura |
| Michler's | ketone is an organic compound with the formula of [(C |
| lohexane, the geminal diol is stable while the | ketone is not. |
| the MPV reaction, oxidation of an alcohol to a | ketone, is termed the Oppenauer oxidation. |
| Perilla | ketone is present in the leaves and seeds of purple m |
| Michler's | ketone is an intermediate in the synthesis of dyes an |
| Diabetic patients can have their | ketone levels tested via urine or blood to indicate d |
| ergoes dehydration to give the α,β-unsaturated | ketone, mesityl oxide: Hydrogenation of mesityl oxide |
| ldehyde monosaccharides may be called aldoses; | ketone monosaccharides may be called ketoses. |
| , and O2, whereas its 4 products are aldehyde, | ketone, nitrite, and H2O2. |
| It is soluble in acetone, methyl ethyl | ketone, nitromethane, and methylene chloride. |
| It is soluble in acetone, methyl ethyl | ketone, nitromethane, and dichloromethane. |
| s the anhydride of oxalic acid or the two-fold | ketone of ethylene oxide. |
| an be regarded as butatriene dione, the double | ketone of butatriene - more precisely 1,2,3-butatrien |
| Codeinone can be also described as the | ketone of codeine: codein-6-on. |
| It can be viewed as a double | ketone of 1,2-dioxetane (1,2-dioxacyclobutane), or a |
| trimer of carbon dioxide (CO2) or as a triple | ketone of 1,3,5-trioxane (1,3,5-trioxacyclohexane). |
| c dimer of carbon dioxide (CO2) or as a double | ketone of 1,3-dioxetane (1,3-dioxacyclobutane). |
| rganic compound with formula C6O6, the sixfold | ketone of cyclohexane. |
| ganic compound with formula C5O5, the fivefold | ketone of cyclopentane. |
| s-isomers are possible for the α,β-unsaturated | ketone, only the trans isomer is observed. |
| er condensation) is the chemical reaction of a | ketone or aldehyde with an α-haloester to form an α,β |
| ct (from "Aldehyde alcohol") is a beta-hydroxy | ketone or aldehyde, and is the product of aldol addit |
| acetone, (or phenyl-2-propanone, benzyl methyl | ketone or methyl benzyl ketone. |
| The reaction product is a | ketone or an aldehyde. |
| , oximes can be used for the identification of | ketone or aldehyde. |
| oxidation is the oxidation of an alcohol to a | ketone or an aldehyde using chromium trioxide and pyr |
| d by deprotonation of a C-H bond adjacent to a | ketone or aldehyde. |
| Reaction of a carbazide with aldehyde or | ketone produces a carbazone. |
| cidosis, the body fails to adequately regulate | ketone production causing such a severe accumulation |
| The oxazaborolidine was first developed as a | ketone reducing agent by the laboratory of Itsuno, an |
| e 1, prostaglandin 9-ketoreductase, xenobiotic | ketone reductase, NADPH-dependent carbonyl reductase, |
| ETN dissolves readily in acetone and other | ketone solvents though for the purpose of recrystalli |
| It is a cyclic | ketone, structurally similar to cyclopentane, consist |
| The Blaise-Maire reaction is the Blaise | ketone synthesis using β-hydroxy acid chlorides to gi |
| The Blaise | ketone synthesis is the chemical reaction of acid chl |
| er with Steven Nahm, he discovered the Weinreb | ketone synthesis, which allows for mono-addition of a |
| to form Weinreb amides for use in the Weinreb | ketone synthesis. |
| e specifically the compound is also a bicyclic | ketone terpene. |
| methylconhydrone is N-methyl-2-piperidyl ethyl | ketone, that DL-conhydrine (mp. |
| The | ketone then undergoes Wolff rearrangement to ketene 6 |
| ction of 1,3-dinitrobenzene with an enolizable | ketone to the Meisenheimer adduct. |
| like Darzens, involves converting methyl nonyl | ketone to its glycidate by allowing it to react with |
| ks include the formation of an α,β-unsaturated | ketone via aldol condensation and hydroxylysinonorleu |
| oteworthy that levels of beta-thujone, a toxic | ketone, were 9.8%, 12.5% and 12.1% in the respective |
| mistry, a selone is the structural analog of a | ketone where selenium replaces oxygen. |
| Piperitone is a natural monoterpene | ketone which is a component of some essential oils. |
| ties of padimate O resemble those of Michler's | ketone which is considered photocarcinogenic in rats |
| 6H4]2CS, is prepared by treatment of Michler's | ketone with hydrogen sulfide in the presence of acid |
| quinone or cyclohexa-3,5-diene-1,2-dione, is a | ketone, with formula C6H4O2. |
| It consists of a 15-membered ring | ketone with one methyl substituent in the 3-position. |
| ynthesized by condensation of an aldehyde or a | ketone with hydroxylamine. |
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