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「ALKENES」の共起表現一覧(1語右で並び替え)

該当件数 : 65



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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