「phenyl」の共起表現(1語右で並び替え)

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共起表現

「phenyl」の共起表現一覧(1語右で並び替え)

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Thus, the two substrates of this enzyme are	phenyl acetate and H2O, whereas its two products are
mide analog, is a synthetic equivalent for the	phenyl anion synthon.
These other carbamates (methyl, butyl, and	phenyl) are only used in small quantities for researc
Note extra	phenyl at right.
From left to right:	phenyl, benzyl, tolyl, o-xylyl.
A simple aryl group is	phenyl, C6H5; it is derived from benzene.
While	phenyl chlorosilanes and many others can be used, met
It is a	phenyl derivative of carbenicillin, acting as a prodr
He prepared it by reduction of a	phenyl diazonium salt using sulfite salts.
SAN, trade name Neo Heliopan AP, INCI disodium	phenyl dibenzimidazole tetrasulfonate) is a water sol
Sodium tetraphenylborate is also employed as a	phenyl donor in palladium-catalyzed cross-coupling re
Ethyl	phenyl ether or phenetole is an organic compound that
Ethyl	phenyl ether has the same properties as some other et
ate reaction product trapped with chloromethyl	phenyl ether, the other chlorine atom in 17 is simply
As shown in the figure below, the	phenyl group at the 2-position can carry different su
ists of a dodecyl group (C12H25) attached to a	phenyl group (C6H5).
The phosphorus is connected to a	phenyl group and two methyl groups.
Enkephalin contains an aromatic	phenyl group on its Phe4 residue, which was hypothesi
a trans ethene double bond substituted with a	phenyl group on both carbon atoms of the double bond.
ane, often abbreviated to BPh3 where Ph is the	phenyl group C6H5-, is a chemical compound with the f
name is derived from the six-carbon, aromatic	phenyl group and the three-carbon propene tail of cin
Ph for the	phenyl group
cetylene is an alkyne hydrocarbon containing a	phenyl group.
H)3, where one OH group has been replaced by a	phenyl group.
For example, the	phenyl groups are the pendant groups on a polystyrene
The plane of the	phenyl groups are perpendicular to the plane of this
the compound lacks oxygen functionalities and	phenyl groups common to other natural or synthetic es
r example, phenytoin (mentioned below) has two	phenyl groups substituted onto the number 5 carbon in
Due to steric interactions, the	phenyl groups are not coplanar and the dihydral angle
The rigidity of the	phenyl groups facilitates packing and elevates the me
henyllithium dimers and the π-electrons of the	phenyl groups in the adjacent dimers.
Due to an inductive effect, the trio of	phenyl groups allows phosphorus to bear such a buildu
It is a hydroxy ketone attached to two	phenyl groups.
es are known where p-toyl replaces some of the	phenyl groups.
wherein two hydrogen atoms are replaced by two	phenyl groups.
midal with a propeller-like arrangement of the	phenyl groups.
n consisting of a central boron atom with four	phenyl groups.
, although with the hydrogen atoms replaced by	phenyl groups.
tion of various side groups (alkyl, alkoxy, or	phenyl) increases the solubility of the polymer and g
	Phenyl is a rude and unfriendly person, who has a bit
CS would appear to be this one: "Isosterism of	phenyl isocyanate and diazobenzene-imide."
	Phenyl isothiocyanate (PITC) is a reagent used in rev
ic acid, acetic anhydride or iodine to produce	phenyl isothiocyanate.
Valerophenone, or butyl	phenyl ketone, is an aromatic ketone.
Evidence for a	phenyl migration in aryne 2 from the 1,2-didehydroben
NMR spectrum for this compound shows that the	phenyl protons are shifted downfield compared to a pr
The parent compound is the	phenyl radical C6H5. .
The parent	phenyl radical has been identified via electron param
osely related to methylphenidate, but with the	phenyl ring replaced by naphthalene.
ng substituents in 3,4, and/or 5 position of a	phenyl ring
(i) by substitution in the	phenyl ring to any extent with alkyl, alkoxy, alkylen
atalyzes the electrophilic substitution of the	phenyl ring with dimethylallyl pyrophosphate (DMAPP)
equilibrium with cyclopropanone B attacks the	phenyl ring through its carbocation forming a transie
uration spanning a few times longer, since the	phenyl ring is directly connected to tropane through
substituted on the aniline	phenyl ring), and derivatives where the N-propionyl g
tain an imidazole ring and a 2,6-dichlorinated	phenyl ring.
tabolized chiefly by para-hydroxylation of the	phenyl ring.
added methyl group in the para position on the	phenyl ring.
group has been added to the 4-position on the	phenyl ring.
(iv) any substitution on the	phenyl rings reduces activity.
Double substitutions of the	phenyl rings are known to occur, even with conversion
is a salt, wherein the anion consists of four	phenyl rings bonded to boron.
Triphenylmethanol contains three	phenyl rings and a hydroxyl group bound to a central
The Li atoms and the ipso carbons of the	phenyl rings form a planar four-membered ring.
of a pyramidal As(III) center attached to two	phenyl rings and one chloride.
The E isomer, in which the two	phenyl rings are cis to each other, is the major prod
The four	phenyl rings are rotated out of the plane compared to
rms a propeller-like conformation in which the	phenyl rings are rotated about 65°, while in the gas
holine ring around the 4-amine group, and both	phenyl rings unsubstituted, was by far the most poten
ecule is subject to reactions typical of other	phenyl rings, including hydroxylation, nitration, hal
Due to steric congestion among the	phenyl rings, the stable conformation of this molecul
omposed of a benzene ring substituted with six	phenyl rings.
Once used in sunscreens,	phenyl salicylate is now used in the manufacture of s
He made	Phenyl salicylate or salol in 1886, and introduced it
In the salol reaction,	phenyl salicylate reacts with o-toluidine in 1,2,4-tr
	Phenyl salicylate, or salol, is a chemical substance,
In AM-251 the p-chloro group attached to the	phenyl substituent at C-5 of the pyrazole ring is rep
C3N2H2Ph)3]-, abbreviated [TpPh]-, wherein the	phenyl substituents project away from the metal.
ompound consisting of a methane core with four	phenyl substituents.
tive intermediates: the aryne 2 is formed from	phenyl substituted phthalic anhydride which rearrange
Although Ph and	phenyl uniquely denote C6H5, substituted derivatives

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