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in turncreatingthe carbonyl group
hot - stage microscopy and DSC screening Leksic E.,PLIVA Inc(passive) discovered bycarbonyl group
of a carbon atom double - bonded to an oxygen atom(passive) is composedA carbonyl group
of a single carbon atom double bonded to a single oxygen atom(passive) is composedA carbonyl group
of a double polar covalent bond between an oxygen atom and a carbon atom(passive) is composedA carbonyl group
of the central carbon atom attached to one oxygen atom by a polar covalent , double bond(passive) is composedThe carbonyl group
The loss of the hydrogen atom connected to methanol 's oxygen atom forces it to double bond with the adjacent carbon atomcreatingthe carbonyl group
of the aldehyde and ketone groups(passive) is composedThe carbonyl group
The presence of this carbon - oxygen double bondcreatesthe carbonyl group
not only from the hydroxyl group at C-3 position , but also at C-2 , C-12 or C-28 positions(passive) can be createdThe carbonyl group
using a hydroxyl class can be instead dual bonded to an o2 chemicalcreatingthe carbonyl group
the immediately N - terminally adjacent residue(passive) contributed bythe carbonyl group
the inductive release of electrons by(passive) caused bythe carbonyl group
photo - oxidation(passive) created bythe carbonyl group
the electronegative character of fluorine(passive) caused bythe carbonyl group
a simple organic compoundcomposedof a carbonyl group
reagent used to fragment peptide chains ... in whichcontributesthe carbonyl group
from one of the terminal carboxyls or from one of the free carboxyls of the aspartic and/or glutamic acids of A and P , the group originating from the dialdehyde structure obtained after oxidation of the carbohydrate structure of P with periodic acidoriginatingfrom one of the terminal carboxyls or from one of the free carboxyls of the aspartic and/or glutamic acids of A and P , the group originating from the dialdehyde structure obtained after oxidation of the carbohydrate structure of P with periodic acid
to C - Nu bond formationleadingto C - Nu bond formation
of double - bonded carbon and oxygen atoms aldehydescomposedof double - bonded carbon and oxygen atoms aldehydes
from the oxidation of celluloseresultingfrom the oxidation of cellulose
the p bond in the C = O to break and allows for neutralisation of the positive chargecausingthe p bond in the C = O to break and allows for neutralisation of the positive charge
from the oxidation of the 12-OH groupresultingfrom the oxidation of the 12-OH group
from its α - carboxy group ) of an amino acid selected from phosphonomethyl - phenylalanine , especially 4-phosphono - methylphenylalanine , phosphono-(α - fluoro)methyl - phenylalanine , especially 4-phosphono-(a - fluoro)methyl - phenylalanineresultingfrom its α - carboxy group ) of an amino acid selected from phosphonomethyl - phenylalanine , especially 4-phosphono - methylphenylalanine , phosphono-(α - fluoro)methyl - phenylalanine , especially 4-phosphono-(a - fluoro)methyl - phenylalanine
from its α - carboxy group ) of an amino acid selected from phosphonomethyl - phenylalanine , especially 4-phosphonomethyl - phenylalanine , phosphono-(α - fluoro)methyl - phenylalanine , esecially 4-phosphono-(α - fluoro)methyl - phenylalanineresultingfrom its α - carboxy group ) of an amino acid selected from phosphonomethyl - phenylalanine , especially 4-phosphonomethyl - phenylalanine , phosphono-(α - fluoro)methyl - phenylalanine , esecially 4-phosphono-(α - fluoro)methyl - phenylalanine
from the oxidation of carbohydrate radicals generated inside the carrageenan polymer [ 38resultedfrom the oxidation of carbohydrate radicals generated inside the carrageenan polymer [ 38
from its α - carboxy group ) of an amino acid selected from phosphonomethyl - phenylalanine , especially 4-hosphono - methyl - phenylalanine , phosphono-(α - fluoro)methyl - phenylalanine , especially 4-phosphono-(α - fluoro)methyl - phenylalanine , phosphono-(α-,α - adifluoro)methyl - phenylalanine , especially 4-phosphono-(α - α - difluro)methyl - phenylalanine , phosphono-(α - hydroxy)methyl - phenylalanine , especially 4-phosphono-(α - hydroxy)methyl - phenylalanine , O - sulfo - tyrosine , such as 4-(O - sulfo)tyrosine , dicarboxymethoxy - phenylalanineresultingfrom its α - carboxy group ) of an amino acid selected from phosphonomethyl - phenylalanine , especially 4-hosphono - methyl - phenylalanine , phosphono-(α - fluoro)methyl - phenylalanine , especially 4-phosphono-(α - fluoro)methyl - phenylalanine , phosphono-(α-,α - adifluoro)methyl - phenylalanine , especially 4-phosphono-(α - α - difluro)methyl - phenylalanine , phosphono-(α - hydroxy)methyl - phenylalanine , especially 4-phosphono-(α - hydroxy)methyl - phenylalanine , O - sulfo - tyrosine , such as 4-(O - sulfo)tyrosine , dicarboxymethoxy - phenylalanine
from one of the terminal carboxyls or the free carboxyls of the aspartic and/or glutamic acids of A and P , the group originating from the dialdehyde structure obtained after oxidation of the carbohydrate structure of P with periodic acidoriginatingfrom one of the terminal carboxyls or the free carboxyls of the aspartic and/or glutamic acids of A and P , the group originating from the dialdehyde structure obtained after oxidation of the carbohydrate structure of P with periodic acid
the C = C bond of the activated propanoyl - CoA to add to the carbon dioxide molecule in an electrophilic mannercausingthe C = C bond of the activated propanoyl - CoA to add to the carbon dioxide molecule in an electrophilic manner
of a carbon double - bonded to an oxygen atomcomposedof a carbon double - bonded to an oxygen atom
a tetrahedral intermediatecreatinga tetrahedral intermediate
in the Carboxylic acids 16resultingin the Carboxylic acids 16
the low electron density at(passive) caused bythe low electron density at
from the CADsoriginatingfrom the CADs
to cyclic structuresleadingto cyclic structures
to the benzenecarboxamide - fluoroquinolones ( BCFQsledto the benzenecarboxamide - fluoroquinolones ( BCFQs
from one of the terminal carboxyls or the free carboxyls of the aspartic and/or glutamic acids of GPIR-1a and P , the --NH-- group originating from one of the terminal amines of GPIR-1a and P or from one of the amines in the epsilon position of one of the lysine residuesoriginatingfrom one of the terminal carboxyls or the free carboxyls of the aspartic and/or glutamic acids of GPIR-1a and P , the --NH-- group originating from one of the terminal amines of GPIR-1a and P or from one of the amines in the epsilon position of one of the lysine residues
to a positive effect on solubility of [ CO . 1 ] which is attributed to free carbonyl groups and ( ii ) another at about 1702 [ cmcontributesto a positive effect on solubility of [ CO . 1 ] which is attributed to free carbonyl groups and ( ii ) another at about 1702 [ cm
from the amide linkage with the sphingoid moiety [ 39resultingfrom the amide linkage with the sphingoid moiety [ 39
from one of the terminal carboxyls or one of the free carboxyls of the aspartic and/or glutamic acids of GPIR-1a and P , the --NH-- group originating from one of the terminal amines of GPIR-1a and P or from one of the amines in the epsilon position of one of the lysine residuesoriginatingfrom one of the terminal carboxyls or one of the free carboxyls of the aspartic and/or glutamic acids of GPIR-1a and P , the --NH-- group originating from one of the terminal amines of GPIR-1a and P or from one of the amines in the epsilon position of one of the lysine residues
carboxamide derivativesto createcarboxamide derivatives
in better overlapresultingin better overlap
to the formation of the corresponding vinyl phosphonatesledto the formation of the corresponding vinyl phosphonates
to the oxyanion formationleadingto the oxyanion formation
The closest protons(passive) influenced byThe closest protons
it to become polarize and picking the H+ of HClcausingit to become polarize and picking the H+ of HCl
to formation of the 4 pi system delocalised over 5 carbons atomsleadingto formation of the 4 pi system delocalised over 5 carbons atoms
to the poor selectivity observedleadsto the poor selectivity observed
in the formation of an imineresultingin the formation of an imine
ring openingcausingring opening
from the terminal carboxyl or the free carboxyls of the aspartic and glutamic acidsoriginatingfrom the terminal carboxyl or the free carboxyls of the aspartic and glutamic acids
in CH2-C =also resultsin CH2-C =
in the formation of the corresponding ( S)- or ( R)- alcohol [ 22,25resultingin the formation of the corresponding ( S)- or ( R)- alcohol [ 22,25
from CO , formate , or acetate ) to proton reductionoriginatingfrom CO , formate , or acetate ) to proton reduction
from diacetonitrile contained in the acrylic copolymer ( A ) , and primary amino groupsoriginatingfrom diacetonitrile contained in the acrylic copolymer ( A ) , and primary amino groups
in a resonance effectresultingin a resonance effect
a portion of each of Formula ( 2 ) and Formula ( 3composinga portion of each of Formula ( 2 ) and Formula ( 3