「ALKENES」の共起表現一覧(1語右で並び替え)
該当件数 : 65件
| Organic reduction of aldehydes, | alkenes, alkynes, nitro compounds, oxiranes to alkene |
| It also chlorinates alkanes, | alkenes, alkynes, aromatics, and epoxides. |
| has been used to selenonate carboxylic acids, | alkenes, alkynes, and nitriles. |
| Thus, π backbonding to | alkenes and CO is stronger for Os compounds, which le |
| dvantageous because of it selectively reduces | alkenes and alkynes and is nonreactive toward many fu |
| a catalyst for the alkylation of alkanes and | alkenes and for the protonation of aromatic compounds |
| and ketones, and for converting epoxides into | alkenes and aldoximes into nitriles. |
| f phosphaalkenes is often compared to that of | alkenes and not to that of imines because the HOMO of |
| l compounds, and to reduce electron-deficient | alkenes and alkynes. |
| Alkenes and π-allyl coordination to palladium(II) ace | |
| s, Grignard reagents, organolithium reagents, | alkenes and amines. |
| Substrates for hydrozirconation are | alkenes and alkynes. |
| Heck reaction between | alkenes and aryl halides |
| nantiomeric excesses from trans-disubstituted | alkenes and trisubstituted alkenes. |
| Cis-disubstituted | alkenes and styrenes are asymmetrically epoxidized us |
| Tellurium tetrachloride reacts with | alkenes and alkynes to the chloro tellurium trichlori |
| anic synthesis for various transformations of | alkenes and alkynes. |
| ertiary alcohols give a substantial amount of | alkenes and ethers as side products. |
| clobutane and methylcyclopropane, but are not | alkenes and are not discussed here. |
| s a reagent for the selective chlorination of | alkenes and alkynes. |
| Generally, the | alkenes are known to react with electrophiles. |
| These branched | alkenes are used to alkylate phenols to give precurso |
| For example, some | alkenes are toxicated by human enzymes to produce an |
| Silver nitrate is used to separate out | alkenes as the η2-alkene complex. |
| elective synthesis of trans-1,2-disubstituted | alkenes based on the condensation of aldehydes with m |
| Ethers are more polar than | alkenes but not as polar as alcohols, esters, or amid |
| ought to be intermediates in the oxidation of | alkenes by permanganate. |
| Alkenes can bind to this site, whereupon they couple | |
| matic hydrocarbons (arenes), alkanes (alkyl), | alkenes, cycloalkanes, alkyne-based; |
| y common classes of organic compounds such as | alkenes, dienes, and alkyl, aryl, and vinyl halides t |
| Alkenes dimerize upon irradiation with UV-light. | |
| and exchanges with alkynes and electrophilic | alkenes, even C60. |
| Cl3 is a specialized Lewis acid in activating | alkenes for the carbonyl-ene reaction and the Diels-A |
| hemist who reported a method for synthesis of | alkenes from aldehydes and ketones using compounds ca |
| s bromine, the heterodiene adds electron-rich | alkenes in Diels-Alder reactions to give dihydropyran |
| Certain diazo compounds can couple to form | alkenes in a formal carbene dimerization reaction. |
| for transforming carbonyl groups to terminal | alkenes, much like the Tebbe reagent or Wittig reacti |
| nation, certain telluroxides (RTeOR) can form | alkenes on heating. |
| Reduction of the | alkenes or π-allyl by coordination to palladium(II) a |
| Therefore like | alkenes, phosphaalkenes engage in Wittig reactions, P |
| To form the root of the IUPAC names for | alkenes, simply change the -an- infix of the parent t |
| This diene reacts rapidly with electrophilic | alkenes, such as maleic anhydride. |
| Difluoroalkenes are | alkenes that have two fluorines on their sp2 carbon. |
| nic chemistry especially in the conversion of | alkenes to 1,2-diols. |
| in oxidation of carbon-carbon double bonds in | alkenes to generate epoxides (oxiranes). |
| ly reduces alkynes and unhindered or strained | alkenes to the corresponding alkenes and alkanes. |
| It adds to | alkenes to afford α-chloro oximes. |
| It adds to | alkenes to give chloride-substituted thioethers. |
| Thiocyanogen adds to | alkenes to give 1,2-bis(thiocyanato) compounds. |
| ICl will also add to the double bond in | alkenes to give chloro-iodo alkanes. |
| intermediate species such as formaldehyde and | alkenes to be emitted. |
| CpFe(CO)2Br reacts with | alkenes to afford cationic alkene-Fp complexes. |
| osulfur chemistry, hydrogen disulfide adds to | alkenes to give disulfides and thiols. |
| most common use for DMDO is the oxidation of | alkenes to epoxides. |
| um tetroxide can similarly be used to oxidize | alkenes to vicinal diols. |
| nyl compounds can also be coupled with simple | alkenes to form five, six or eight membered rings. |
| the alkylate depends mainly upon the kind of | alkenes used and upon operating conditions. |
| Jacobsen epoxidation of | alkenes using manganese-salen complex and NaOCl |
| Shi epoxidation of | alkenes using oxone and a fructose-derived chiral cat |
| Sharpless asymmetric dihydroxylation of | alkenes using dihydroquinine or dihydroquinidine liga |
| r in the cobalt-catalyzed hydroformylation of | alkenes, where it greatly increases the ratio of stra |
| tructural isomers (cycloalkanes and aliphatic | alkenes) which share the general formula of C5H10. |
| There are also cyclic | alkenes with four carbon atoms overall such as cyclob |
| Pentene refers to all the | alkenes with chemical formula C5H10. |
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