「ethers」の共起表現一覧(1語右で並び替え)
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| hosphine) and assists the synthesis of esters, | ethers, amines and thioethers of alcohols. |
| Hydrocarbon mixtures are composed of petroleum | ethers and other hydrocarbons. |
| They can be easily protected with MTM | ethers and recovered in good yield. |
| aliphatic hydrocarbons, ethyl acetate, glycol | ethers, and acetone. |
| olvent properties of lower molecular weight of | ethers and alcohols. |
| n eliminated completely, however such items as | ethers and potions do appear in the game to be used o |
| s alcohols and carboxylic acids into the silyl | ethers and silyl esters, respectively. |
| methyl compounds, particularly trifluoromethyl | ethers and trifluoromethyl aromatics, are converted i |
| sed with the class of organic compounds called | ethers; and equally, going under its alternative name |
| ted him to enter the domain of these superfine | ethers, and become familiar with their mysteries. |
| int (175-325°C) than gasoline or the petroleum | ethers, and a lower boiling point than the oils. |
| Ethers are slightly polar. | |
| Crown | ethers are useful as phase transfer catalysts. |
| 3,4-Dimethoxybenzyl | ethers are produced in the same ways. |
| Glycol | ethers are a group of solvents based on alkyl ethers |
| Crown | ethers are not the only macrocyclic ligands that have |
| Various silyl | ethers are also popular protecting groups for several |
| toxic) mercuric chloride, to which most other | ethers are stable. |
| polyphenyl and fluorinated | ethers are the "raw materials" for Nye lubricants. |
| Ethers are more polar than alkenes but not as polar a | |
| ohols give a substantial amount of alkenes and | ethers as side products. |
| unctional molecules becomes possible using MTM | ethers as the protective groups for their hydroxyl gr |
| e in the 1960s with the synthesis of the crown | ethers by Charles J. Pedersen. |
| Depending on the substituents, some | ethers can be cleaved with a variety of reagents, e.g |
| d for the production of perfluorinated amines, | ethers, carboxylic acids, and sulfonic acids. |
| In contrast to crown | ethers, cryptands bind the guest ions using both nitr |
| Like crown | ethers, cyclen compounds are capable of selectively b |
| Unlike most | ethers, does not form peroxides on storage |
| mediate in the synthesis of glycerol, glycidyl | ethers, esters and amines. |
| f nucleophiles, including enolates, enol silyl | ethers, Grignard reagents, organolithium reagents, al |
| Perhaps the most common use of halogenated | ethers has been in anesthesiology. |
| MTM | ethers have another advantage. |
| the synthesis and binding properties of crown | ethers in a seminal series of papers. |
| eophiles and the use of triisopropylsilyl enol | ethers in organic synthesis. |
| s are based on a formula containing diglycidyl | ethers, including BADGE. |
| suggests that occupational exposure to glycol | ethers is related to low motile sperm count in men, b |
| e Selexol solvent is a mixture of the dimethyl | ethers of polyethylene glycol. |
| readily available commercially as solutions of | ethers or hydrocarbons; it is not usually prepared in |
| The reaction of enolates, enol | ethers, or enol acetates with NBS is the preferred me |
| iting the blending of gasoline with "alcohols, | ethers, or other oxygenates." |
| Some | ethers rapidly cleave with boron tribromide (even alu |
| options of anesthesiologists, but halogenated | ethers remain a mainstay of general anesthesia. |
| Schedules I and II to include isomers, esters, | ethers, salts of isomers, esters and ethers, and any |
| yl ether has the same properties as some other | ethers, such as volatility, explosive vapors, and the |
| xplosions when tert-butyllithium is mixed with | ethers such as diethyl ether, tetrahydrofuran, and gl |
| Ethers susceptible to this reaction, a typical exampl | |
| reacts faster with t-butyldimethysilyl (TBDMS) | ethers than triisopropylsilyl (TIPS) ethers. |
| the para-methoxybenzyl and 3,4-dimethoxybenzyl | ethers, the former are generated by treatment of the |
| It also reacts with alcohols to give methyl | ethers, where diazomethane may not. |
| are created by the reaction of P4S10 with aryl | ethers which are different from anisole. |
| ids (RR'-O+-C-R'R) are prepared by reaction of | ethers with diazo compounds. |
| Fatty alcohol polyglycol | ethers with a narrow homolog distribution, which are |
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