「allyl」の共起表現一覧(1語右で並び替え)
該当件数 : 46件
Substitution of the acetate group in | allyl acetate using hydrogen chloride yields allyl c |
Other routes are from butadiene, | allyl acetate and succinic acid. |
Allyl alcohol is the smallest representative of the | |
Allyl alcohol is also produced primarily from allyl | |
Allyl alcohol is used as a raw material for the prod | |
iety of polymerizable esters are prepared from | allyl alcohol, e.g. |
Hydrolysis of this acetate gives | allyl alcohol. |
Glycidol is prepared by the epoxidation of | allyl alcohol. |
solid is related to catechol by attachment to | allyl alcohol. |
Sharpless epoxidation of | allyl alcohols using titanium isopropoxide, diethyl |
tannane additions (nucleophilic addition of an | allyl-, allenyl-, or propargylstannanes to an aldehyd |
ene:diethyl ether), the epoxide is opened with | allyl amine to yield the corresponding 1,2-amino alc |
salt gives the corresponding neutral hydride, | allyl, and nitrosyl (see figure) derivatives. |
fer-RNA Nucleoside Queuosine by Using a Chiral | Allyl Azide Intermediate“, Angewandte Chemie Interna |
bromodan from | allyl bromide |
prepared via the free radical addition between | allyl bromide and hydrogen bromide. |
esized in the normal method from magnesium and | allyl bromide. |
Allyl caproate is an ingredient of some lipstick per | |
ompounds of the type [(η3-allyl)Fe(CO)4+X- are | allyl cation synthons in allylic substitution . |
Allyl chloride is generally produced directly by the | |
For instance treatment with | allyl chloride gives [MoCl(allyl)(CO)2(MeCN)2], wher |
Allyl chloride undergoes dehydrohalogenation upon tr | |
yzed by the White catalyst which accesses a Pd | allyl complex via allylic C-H cleavage rather than b |
Allyl compounds with suitable leaving groups react w | |
h hydrogen cyanide over copper catalyst yields | allyl cyanide. |
Allithiamine (INN), or thiamine | allyl disulfide (TAD), is a lipid-soluble form of vi |
ol (BAN/INN), also known as allyloestrenol and | allyl estrenol, is a synthetic progestogen sometimes |
tion involving the thermal rearrangement of an | allyl group which eventually became known as the Cop |
s an Grignard reagent used for introducing the | allyl group. |
The presence of the | allyl groups allows the polymer to form cross-links; |
omers with methyl, ethyl, propyl, isopropyl or | allyl groups. |
Allyl halides react with Ni(CO)4 to form pi-allyl co | |
Allyl hexanoate is a colorless to pale yellow clear | |
Allyl hexanoate is employed principally in the formu | |
Allyl isothiocyanate can also be liberated by dry di | |
Allyl isothiocyanate (AITC) is the organosulfur comp | |
Synthetic | allyl isothiocyanate is used as an insecticide, bact |
Allyl isothiocyanate comes from the seeds of black m | |
d oil is 8007-40-7, and the CAS number of pure | allyl isothiocyanate is 57-06-7. |
myrosinase degrades sinigrin to a mustard oil ( | allyl isothiocyanate), which is responsible for the |
s on a glucosinolate known as sinigrin to give | allyl isothiocyanate. |
Allyl methyl sulfide (AMS) is an organosulfur compou | |
These compounds in turn are sources of | allyl nucleophiles. |
Cyclopentadienyl | allyl palladium is produced by the reaction of allyl |
is reagent reacts with propene to the compound | allyl potassium (KCH2CHCH2). |
Ball-and-stick model of the | allyl silatrane molecule |
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