「CARBONS」の共起表現(1語右で並び替え)

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意味

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共起表現

「CARBONS」の共起表現一覧(1語右で並び替え)

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of the carbon atoms indicates the fate of the	carbons according to their position in fructose 6-pho
inyl bromide are added to (7) to add two more	carbons and form (8). The final step is the addition
olecule has two stereocentres (two asymmetric	carbons), and can exist as three different stereoisom
bles a benzene ring, except that two adjacent	carbons are replaced by nitrogen and boron, respectiv
The bond angles on the shared	carbons are considerably strained: three of them are
Hexoses, which are sugars which contain six	carbons, are not dehydrated to furfural, and so they
rminal monofluoroalkanes with even numbers of	carbons are ultimately metabolized into fluoroacetate
Activated	carbons are complex products which are difficult to c
Bonded to the cyclic chain of	carbons are four nitrogen atoms facing the center of
OH), with the exception of the first and last	carbons, are asymmetric, making them stereocenters wi
carbon is sp-hybridized, and the two terminal	carbons are sp2-hybridized.
in, where 5' and 3' refer to the numbering of	carbons around the ribose ring which participate in f
The ring contains an imine bond, and the	carbons at the 4 and 5 positions are singly bonded, r
polar functionally bonded silicas with short	carbons chains frequently makes up the solid phase.
Since this drug contains 2 chiral	carbons, clearly there is 4 possible isomers: (SS), (
	Carbons containing vicinal functional groups are mark
The benzyl	carbons deviate by another 20.2°.
In this case there are two rings with two	carbons each and a single bridge with one carbon, exc
riglycerides (MCTs) are medium-chain (6 to 12	carbons) fatty acid esters of glycerol.
xylic acid group and five to nine fluorinated	carbons function as fluorosurfactants.
The bonds of the shared	carbons have an inverted tetrahedral geometry; the co
th two phosphate groups attached to different	carbons in the ribose ring.
l of the myristic acid molecule (there are 13	carbons in the tail, 14 carbons in the entire molecul
i.e. the double bond is between the #1 and #2	carbons in the molecule.
Additionally, the positions of the	carbons in the ribose sugar that forms the backbone o
e numerical prefix, which lists the number of	carbons in each ring, excluding the carbons that are
ed first, which indicates the total number of	carbons in both rings including the carbons making up
to form a linear chain of 32 carbon atoms (40	carbons including methyl sidechains).
without the central bond and unfilled central	carbons) is calculated to be 80 kcal/mol higher.
As a result, eight	carbons is the minimum ring size required to form a t
fact that there is a double bond between the	carbons is implicit because carbon has a valence of f
The bond angle formed by the three	carbons is 180°, indicating linear geometry for the c
cks either of the electron deficient carbonyl	carbons, losing hydrogen and protonating the oxygen.
ty of solids such as heterogeneous catalysts,	carbons, metal powders, soils, ceramics, active pharm
The Li atoms and the ipso	carbons of the phenyl rings form a planar four-member
introduction of double bonds between defined	carbons of the fatty acyl chain.
e protein backbone is shown in red, the alpha	carbons of the eight cysteine residues in green, and
cause the methylene unit is delivered to both	carbons of the alkene simultaneously, the configurati
eaction has been used to release the carboxyl	carbons of bone collagen from ancient bones for stabl
Numbered ribose	carbons on cytidine.
recursor farnesyl diphosphate [A] contains 15	carbons, or 3 isoprene units.
on fibers and filaments, graphites, activated	carbons, pyrolytic carbons, glass-like carbons, carbo
ize the couplings between protons on adjacent	carbons, reducing problems with magnetic inequivalenc
The important	carbons relative to the transformation are numbered f
lecule and an acyl CoA molecule, which is two	carbons shorter.
fferent stereoisomerisation around the chiral	carbons, so for now I've reverted to the version whic
ger bridging distance between the two allylic	carbons than their respective cis-cycloalkenes.
is relieved by pyramidalization of the alkene	carbons, the pyramidalization angle is estimated at 3
In conventional nomenclature, the	carbons to which the phosphate groups attach are the
In alkanes, the ratio of	carbons to hydrogens is CnHn+2.
In organic species that already have oxidized	carbons via the presence of oxygen, a weaker signal i
um chain fatty acids (Fatty acids having 6-12	carbons) while reducing FAD to FADH2
ed anywhere between three to as many as seven	carbons, with highest potency usually seen with the p
t elimination of the terminal and subterminal	carbons, yielding a fatty acid that is one carbon sho

共起表現

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「CARBONS」の共起表現一覧(1語右で並び替え)