「ethers」の共起表現一覧(1語右で並び替え)

ethers

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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