「Epoxide」の共起表現一覧(1語右で並び替え)
該当件数 : 43件
Heptachlor and its | epoxide absorb to soil particles and evaporate. |
The | epoxide also dissolves more easily in water than its |
DNA attacks the | epoxide, and is bound permanently to it. |
Thus, the two substrates of this enzyme are | epoxide and H2O, whereas its product is glycol. |
dol is an organic compound that contains both | epoxide and alcohol functional groups. |
o oxidize vitamin K hydroquinone to vitamin K | epoxide at the same time; the carboxylation and epoxi |
a two-step method, converting an olefin to an | epoxide before its conversion to the episulfide using |
ive tracts of insects, aldrin oxidizes to the | epoxide dieldrin, which is more strongly insecticidal |
e lactone containing two lactone rings and an | epoxide functional group, and it has shown to have an |
te, which is juvenile hormone III lacking the | epoxide group. |
Other names in common use include | epoxide hydrase (ambiguous, epoxide hydratase (ambigu |
Other names in common use include | epoxide hydratase (ambiguous), microsomal epoxide hyd |
Epoxide hydrolase (also known as epoxide hydratase) f | |
Epoxide hydrolase is present in large quantity on end | |
In enzymology, a microsomal | epoxide hydrolase (EC 3.3.2.9) is an enzyme that cata |
In enzymology, a soluble | epoxide hydrolase or sEH (EC 3.3.2.10) is an enzyme t |
pid phosphatase, sEH (ambiguous), and soluble | epoxide hydrolase (ambiguous). |
Other names in common use include hepoxilin | epoxide hydrolase, hepoxylin hydrolase, and hepoxilin |
The systematic name of this enzyme class is | epoxide hydrolase. |
lation, which triggers a rearrangement of the | epoxide into a carbonyl (4). |
The corresponding | epoxide is formed under basic conditions with potassi |
Heptachlor | epoxide is more likely to be found in the environment |
-dibromoethane in benzene:diethyl ether), the | epoxide is opened with allyl amine to yield the corre |
e into DNA and alkylate the bases through its | epoxide moiety. |
The | epoxide of tetrafluoroethylene is even more unstable |
This colourless gas is the | epoxide of hexafluoropropylene, that is fluorinated a |
It is the sulfur analogue of an | epoxide or aziridine. |
When these are kneaded together an | epoxide polymerisation reaction is catalysed. |
Alternately, other | epoxide rearrangements can be induced to form other s |
ely due to inhibition of the enzyme vitamin K | epoxide reductase) and a reaction with ethanol simila |
ely due to inhibition of the enzyme vitamin K | epoxide reductase)(vitamin K supplement is recommende |
The opening of the | epoxide ring with LiTEBH proceeds with exceptional re |
e alkene starting material is retained in the | epoxide ring of the product. |
rmation of the carbon-carbon connectivity and | epoxide ring in a single reaction. |
the primary hydroxyl group (carbon 8) and the | epoxide ring (carbons 4 and 5). |
tetracyanoethylene oxide, an electrophilic | epoxide that undergoes ready scission of its C-C bond |
reaction of cyclohexene with mCPBA to give an | epoxide; the reaction mechanism is not shown. |
The | epoxide then undergoes a retro-Diels-Alder reaction, |
notice is that those mechanisms which have a | epoxide to be an intermediate are excluded,which shou |
Opening of the | epoxide under reductive conditions present in cells c |
Industrially, it can be used to determine the | epoxide value of various adhesives. |
E-64 is an | epoxide which can irreversibly inhibit a wide range o |
by reaction of an | epoxide with carbon dioxide catalysed by a zinc halid |
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