ライフサイエンスコーパス: carbonyl

1 ted in elevated levels of CYP2E1 and protein carbonyls).

2 4 formation is the hydrogenation of adsorbed carbonyl.

3 lysine NH3(+) group interacts with backbone carbonyl.

4 -bound hydroxide ion onto the ceramide amide carbonyl.

5 inst modifications produced by lipid-derived carbonyls.

6 r-UV irradiation, led to complete release of carbonyls.

7 nitial reaction of GSH with Michael-acceptor carbonyls.

8 ortant glutamate and three rings of backbone carbonyls.

9 d in food products by lipid-derived reactive carbonyls.

10 e of the steric hindrance exerted by the two carbonyls.

11 them the 10-(4-(3-methoxyphenyl)piperazine-1-carbonyl)-10H-phenoxazine-3-carbonitrile (16o), showed e

12 gen bonds between Calpha-H carbon donors and carbonyl acceptors on opposing helices (Calpha-H...O hor

13 The carboxyl, carbonyl, acetyl groups were determined in modified star

14 including monoacids, diacids, hydroxy acids, carbonyl acids, and aromatic acids.

15 ino diketone system allied to the Lewis acid carbonyl activator BF3 were strategically employed for t

16 s that engage transient diones in successive carbonyl addition.

17 Unlike classical carbonyl additions, stoichiometric organometallic reagen

18 al lineO) behave as (phosphino)phosphinidene-carbonyl adducts (>P-P<--:C horizontal lineO).

19 d sterically large ketenes, and results in a carbonyl alkene complex.

20 nd dimerization of the resultant alpha-amino carbonyls all complicated the syntheses of the dihydro-4

21 We report decarboxylative carbonyl alpha-arylation by coupling arylboron nucleophi

22 carbonyls can be produced more rapidly than carbonyl-amine reactions, therefore providing a satisfac

23 food quality and safety as a consequence of carbonyl-amine reactions.

24 -diazo-5-oxo-2-(((phenyl(pivaloyloxy)methoxy)carbonyl)amino)hexanoate (13d), was stable in swine and

25 ethyl-4-(((1(R)-(3-(11)C-methylphenyl)ethoxy)carbonyl)amino)isoxazol-5 -yl)-[1,1'-biphenyl]-4-yl)cycl

26 -(3-{1-carboxy-5-[(6-(18)F-fluoro-pyridine-3-carbonyl)-amino]-pentyl}-ureido)-p entanedioic acid) and

27 -11, 2-(3-{1-carboxy-5-[(6-fluoro-pyridine-3-carbonyl)-amino]-pentyl}-ureido)-pentaned ioic acid (DCF

28 e that involvement of the peptide backbone's carbonyl and amide groups in hydrogen-bond stabilization

29 In cases where both carbonyl and amine show high reactivity, it is possible

30 The contents of the carbonyl and carboxyl groups in a starch molecule theref

31 ne products generally formed in reactions of carbonyl and dicarbonyl compounds with H2 O2 were not de

32 ines have dramatically expanded the scope of carbonyl and iminyl chemistry by facilitating reactions

33 Favorable interactions with carbonyl and tail groups of phospholipids stabilize Hg-c

34 ecific electrostatic interaction between the carbonyl and the azide beta-nitrogen, which stabilizes t

35 Allylboronic esters react readily with carbonyls and imines (pi-electrophiles), but are unreact

36 tryptophan loss and the formation of protein carbonyls and iron had a clear dose-effect in most syste

37 zyme activity but reduced protein oxidation (carbonyls) and the concentration of IL-1beta, IL-6, TNF-

38 ide increased with increasing DOM aromatic-, carbonyl-, and carboxyl-C content.

39 functional group fractions (including acids, carbonyls, aromatics, and aliphatics) were calculated to

40 ecular radical aziridination of this type of carbonyl azides, allowing for high-yielding formation of

41 In the ester carbonyl band, the effect of changing temperature on bot

42 ing ylide then rearranges, using an internal carbonyl base, to form an enol that leads to the product

43 ior performance of isatins compared to other carbonyl based dienophiles was demonstrated and rational

44 oxy-1-phenyl-3,4-tetrahydroisoquinoline-1H-2-carbonyl)benzenes ulfonamide (30) exhibited a remarkable

45 hCA II with 4-(3,4-dihydro-1H-isoquinoline-2-carbonyl)benzenesulfonamide (3) (PDB code 4Z1J ), a nove

46 es of 4-(1-aryl-3,4-dihydro-1H-isoquinolin-2-carbonyl)benzenesulfonamides (23-33) was designed.

47 A new one-pot approach to construct alpha-carbonyl bicyclic furans from easily accessible diynones

48 i-p-topyldiaryldi(2-pyrrolyl)methane)bis(2,2'carbonyl)bis(azanediyl )) diethaneamine.2HCl] (8) select

49 For 2, rotations about the pentiptycene-carbonyl bond (the alpha rotation) and about the aryl-ca

50 bond (the alpha rotation) and about the aryl-carbonyl bond (the beta rotation) are independent, and t

51 erates the active trans-isomer competent for carbonyl bond activation by active-site residues, thereb

52 The metal-carbonyl bond has partial double bond character accordin

53 ggested to modify the lipid-derived reactive carbonyl but not the reaction mechanism because the Ea o

54 ations involving radicals derived from amide carbonyls by single electron transfer take place under m

55 ed by single electron transfer to amide-type carbonyls by SmI2-H2O-LiBr, provide efficient access to

56 de evidence consistent with the reduction of carbonyls by SmI2-water proceeding through proton-couple

57 compositions (alkyl, O-alkyl, aromatic, and carbonyl C) in SOC.

58 l reactions involving lipid-derived reactive carbonyls can be produced more rapidly than carbonyl-ami

59 rate limiting and results in an intermediate carbonyl carbene complex.

60 s well as for the selective cyanation of the carbonyl carbon atom linked to the N atom of proline res

61 Cys, Ser, or Thr side chain and the backbone carbonyl carbon to form a thiazoline, oxazoline, or meth

62 The synthesis of alpha-amino carbonyl/carboxyl compounds is a contemporary challenge

63 eristic of Snn are the two downfield shifted carbonyl chemical shifts, the chemical shift correlation

64 alkene instead of npi* excited state of the carbonyl chromophore in a "transposed Paterno-Buchi" rea

65 ysis of six standards representing different carbonyl classes, acetaldehyde could be ionized only aft

66 Dehydration, carbonyl cleavage, and redox reactions turned out to hav

67 The binding of organometallic osmium carbonyl clusters onto the surface of gold nanoparticles

68 proximately hydroxyl (OH) > nitrate (ONO2) > carbonyl (CO) approximately ester (COO) > methylene (CH2

69 CORP-1) incorporates 1 such that neither the carbonyl complex nor its photoproduct(s) exits the polym

70 Group 6 metal carbonyl complexes ([M(bpy)(CO)4], M = Cr, Mo, W) are po

71 ons between low-valent Rh(I) and Ir(I) metal-carbonyl complexes and arylnitrile oxides possess the el

72 scribe the synthesis of reduced iron-hydride/carbonyl complexes that enable an electrophile-promoted

73 Competing reductive homocoupling of the carbonyl component is suppressed.

74 nd, avoiding in this way the reaction of the carbonyl compound with the amino acid.

75 related to their ability to trap rapidly the carbonyl compound, avoiding in this way the reaction of

76 closure between a beta-arylethylamine and a carbonyl compound.

77 d on the condensation between an amine and a carbonyl compound.

78 the in situ Bronsted acid activation of the carbonyl compound.

79 man saliva strongly decreased the release of carbonyl compounds (aldehydes and ketones).

80 e extraction and UFLC-DAD-ESI-MS analysis of carbonyl compounds (CCs) in oils heated to 180 degrees C

81 o esters by the reaction of a broad range of carbonyl compounds and aldimines are disclosed.

82 mote the Michael reaction between enolizable carbonyl compounds and nitroolefins with excellent enant

83 ct relationship between the concentration of carbonyl compounds and trigeminal burn.

84 s, allylmagnesium reagents reacted with most carbonyl compounds at similar rates.

85 g reactions of aryl groups with alpha-fluoro carbonyl compounds catalyzed by palladium complexes have

86 allows direct access to chiral beta-alkynyl carbonyl compounds employing allylic alcohol substrates

87 oach to the asymmetric synthesis of valuable carbonyl compounds from easily accessed starting materia

88 tion of various alkyl aryls to corresponding carbonyl compounds has also been reported.

89 Carbonyl compounds have traditionally been detected spec

90 nation experiments revealed that addition of carbonyl compounds increased trigeminal burn perception

91 carbenoid insertion reaction of alpha-diazo carbonyl compounds into Si-H and S-H bonds was developed

92 terials in the hydrogenation of nitriles and carbonyl compounds is strongly influenced by the modific

93 which are precursors to valuable beta-amino carbonyl compounds such as beta-amino amides and esters,

94 aliphatic nitriles to alpha,beta-unsaturated carbonyl compounds under mild, neutral conditions is rep

95 e-2-carbaldehydes, primary amines, and diazo carbonyl compounds under Rh(II) catalysis.

96 In addition to activated carbonyl compounds viz.

97 yse the reductive coupling of a broad set of carbonyl compounds with a variety of primary and seconda

98 ) F]trifluoromethylthiolation of alpha-bromo carbonyl compounds with broad substrate scope and compat

99 omplexity associated with the interaction of carbonyl compounds with hydroperoxides and H2O2 in acidi

100 ols, 11 acids, 39 esters, 8 hydrocarbons, 14 carbonyl compounds, 17 terpenes, and 6 other compounds.

101 novel strategy for the utilization of simple carbonyl compounds, aldehydes and ketones, as intermolec

102 tween electronically or sterically different carbonyl compounds, allylmagnesium reagents reacted with

103 -catalyst for the hydrosilative reduction of carbonyl compounds, and in most cases at room temperatur

104 that additions of allylmagnesium halides to carbonyl compounds, unlike additions of other organomagn

105 e tool for the alpha- and beta-activation of carbonyl compounds, via HOMO, SOMO or LUMO activation pa

106 d and the substrate scope extended to benzyl carbonyl compounds.

107 new tool to convert alkenes into beta-amino carbonyl compounds.

108 eta-aminocyano(MIDA)boronates from borylated carbonyl compounds.

109 2 in THF and the addition reactions of 2 to carbonyl compounds.

110 old starts induce high emissions of BTEX and carbonyl compounds.

111 n of protein amino and guanidino groups with carbonyl compounds.

112 ve DPF emit fewer particles but more NOx and carbonyl compounds.

113 C(sp(3))-H alkylation of saturated aliphatic carbonyl compounds.

114 e, toluene, ethylbenzene, and xylene (BTEX); carbonyl compounds; and polycyclic aromatic hydrocarbons

115 Samples with reduced carbonyl concentrations had significantly lower perceive

116 ation method enables one to identify various carbonyl containing functional groups by infrared spectr

117 lative contributions of two broad classes of carbonyl-containing compounds, ketones/aldehydes versus

118 stidine, cysteine, or lysine residues to the carbonyl-containing histidine oxidation intermediates to

119 tuted THQ analogues that incorporate various carbonyl-containing moieties to maintain DOR affinity an

120 as a linchpin to introduce a broad range of carbonyl-containing pharmacophores onto oligopeptides, t

121 electivity for the formation of multi-carbon carbonyl-containing products, which we hypothesize to be

122 An approach to access azaborininones (carbonyl-containing, boron-based heterocyclic scaffolds)

123 method resulted in three to fourfold larger carbonyl content determined in chicken, pork and beef (2

124 nd finally a Pictet-Spengler reaction with a carbonyl cosubstrate.

125 -diethylamino-3-((((2-maleimidyl)ethyl)amino)carbonyl) coumarin) placed at the same positions, which

126 ed annulation chemistry where initial alkyne-carbonyl coupling is followed by a second, now intramole

127 Herein, carbonyl cyanide m-chlorophenyl hydrazone (CCCP)-induced

128 function induced by mitochondrial ionophore, carbonyl cyanide m-chlorophenyl hydrazone and other resp

129 translocation to mitochondria in response to carbonyl cyanide m-chlorophenylhydrazone treatment.

130 Unlike the protonophore carbonyl cyanide m-chlorophenylhydrazone, which activate

131 ol ROS bursts after high-dose treatment with carbonyl cyanide m-chlorophenylhydrazone.

132 Moreover, in the presence of carbonyl cyanide-p-trifluoromethoxyphenylhydrazone (FCCP

133 cascade triggered by reduction of amide-type carbonyls delivers novel, complex tetracyclic architectu

134 lkynyl halo-Prins reaction joins an enyne, a carbonyl derivative, and either a chloride, bromide, or

135 philes for the synthesis of beta-substituted carbonyl derivatives.

136 It undergoes carbonyl displacement chemistry with various donors (L),

137 ts that with the exposure to radiations, the carbonyl double bonds break affording oxo-radicals that

138 onstrate that zinc homoenolates can react as carbonyl-electrophiles in the presence of nucleophilic a

139 tion of GSH with nine alpha,beta-unsaturated carbonyls employing high performance liquid chromatograp

140 When combined with intramolecular carbonyl-ene reaction (ICE), the accessibility of the na

141 species were identified by NMR from distinct carbonyl environments resonating at deltaC approximately

142 However, reactive carbonyls exhibit significantly less spatial variability

143 tadienyl and carboranyl ligands on the metal carbonyl, explain the ease of the chemical processes and

144 water network to selectively activate the C9 carbonyl for nucleophilic addition.

145 : reduced tryptophan fluorescence intensity, carbonyl formation, and extensive polymerization of myos

146 superposition of similar absorption bands of carbonyl functional groups summing up to a broad, nondis

147 s developed to date for the hydrogenation of carbonyl functionalities (loadings up to approximately 1

148 Chemoselective activation of amide carbonyl functionality and subsequent umpolung via N-oxi

149 lectron-rich arenes to the alpha-position of carbonyl functionality of in situ generated masked benzo

150 hese compounds have an additional conjugated-carbonyl-functionality.

151 This methodology generates alpha-carbonyl-functionalized dihydroisobenzofuran derivatives

152 pective is focused on alpha,beta-unsaturated carbonyls given their preponderance in bioactive natural

153 ation kinetics between adsorbed formates and carbonyls governs the selectivities to CH4 and CO.

154 designed by bioisosteric replacement of the carbonyl group at position 2 in a series of 3,4-dihydrop

155 Thr196 residue of SpnF and the substrate C15 carbonyl group contributes to the enhancement of the rat

156 We describe the consequence of the 6-carbonyl group deletion in N-methylmorphinan-6-ones 1-4

157 xtures of diasteromers and all of them had a carbonyl group in a free form or as hemiacetal.

158 The carbonyl group in butenolide holds the position of thiop

159 antagonists identified herein and a backbone carbonyl group in transmembrane domain 4.

160 rophile preorganization by coordination to a carbonyl group likely play a role in controlling the rea

161 ety being the most preferred followed by the carbonyl group of aryl aldehyde and the aryl methane.

162 The pi --> pi* transition of the carbonyl group of the o-methylbenzaldehyde correlates wi

163 Metabolites containing a carbonyl group represent several important classes of mo

164 ncreases the susceptibility of a coordinated carbonyl group to nucleophilic addition in the former, f

165 f the amide spacer and the direct linkage of carbonyl group to the gamma-pyrone ring, along with the

166 favored by the coordination of the phenacyl carbonyl group to the lanthanide center.

167 unctionality of the oxygen atom of the ester carbonyl group via noncovalent interaction, which provid

168 The reaction involves methylenation of the carbonyl group with tetrahydrothiophenium ylide followed

169 abilization of carbene intermediates via the carbonyl group.

170 two different silicon groups rather than the carbonyl group.

171 hich may be ascribed to the influence of the carbonyl group.

172 Recent strategies for installing reactive carbonyl groups and alpha-nucleophiles into biomolecules

173 solvation effect as well as on the number of carbonyl groups available for further Li binding.

174 -ion battery electrodes with carboxylate and carbonyl groups have been widely studied.

175 scalar couplings between methyl and backbone carbonyl groups in proteins.

176 -) charge-dipole attraction compel the amide carbonyl groups to orient antiperiplanar to the C-F bond

177 Samples were dried under vacuum, and carbonyl groups were protected with methoxylamine.

178 evaluated on protein oxidation (by measuring carbonyl groups), protein nitrosation (by measuring nitr

179 yclized GNRs induces cleavage of sacrificial carbonyl groups, resulting in atomically well-defined he

180 ps of starch molecules are first oxidized to carbonyl groups, then to carboxyl groups.

181 e radical scavenging capacity, protein-bound carbonyl groups, thiol groups and metal chelation activi

182 mistry, alcohols are important precursors to carbonyl groups, which then can be converted into a wide

183 terms of direct alkylation reactions of some carbonyl groups.

184 ations involving orbitals extending onto the carbonyl groups.

185 The use of (13)CO-enriched ruthenium carbonyl has demonstrated that the boron-bound carbon at

186 ketones to optically enriched alpha-indolic carbonyls has been accomplished using a new amino alcoho

187 onolayer functionalized with a rhenium metal carbonyl headgroup on an SiO2 surface.

188 ents on a water-soluble version of the metal carbonyl headgroup shows that water hydrogen bond rearra

189 evealed a different kinetics for lipid ester carbonyl hydration, suggesting that the carboxyl is link

190 yl azodicarboxylate leads to an intermediate carbonyl imide, which can react with a variety of amines

191 ion-metal-catalyzed addition of C-H bonds to carbonyls, imines, and related polarized pi bonds has em

192 ion-metal-catalyzed addition of C-H bonds to carbonyls, imines, and related polarized pi bonds.

193 centers beta, gamma, and delta relative to a carbonyl in high enantioselectivity.

194 level measuring overall two to fourfold more carbonyls in muscles from different species as well as i

195 ons of ammonia or ammonium sulfate (AS) with carbonyls in secondary organic aerosol (SOA) produced fr

196 by thioethers mimic the alternating sites of carbonyls in the poly-beta-ketone intermediates.

197 l as the use of photoactive transition metal carbonyls in the presence of alkyl, fluoroalkyl, and per

198 id cycle enzyme aconitase and higher protein carbonyls; in both, lower glycolytic enzyme enolase.

199 f oxidized compounds, for example, acids and carbonyls increased.

200 bond possible as the attack on the aldehyde carbonyl is too high in energy.

201 5, the first example of a molecular thorium carbonyl isolable at room temperature.

202 O)6 , the only paramagnetic homoleptic metal carbonyl isolable under ambient conditions.

203 THF into water and CO, thereby providing the carbonyl ligand for hydrogenase.

204 ously, to a dark state (nOpi*) involving the carbonyl lone pair.

205 DNA damage induced by reactive carbonyls (mainly methylglyoxal and glyoxal), called DNA

206 of proteins, lactate dehydrogenase, protein carbonyl (marker of ROS), 3-nitrotyrosine (marker of RNS

207 o-caproyl-valine-citruline-p-amino-benzyloxy carbonyl (mcVC-PABC).

208 ary and an online search program for labeled carbonyl metabolite identification based on MS, RT, and

209 e possibility of detecting a large number of carbonyl metabolites as well as high reproducibility of

210 e use of dansylhydrazine (DnsHz) labeling of carbonyl metabolites to change their chemical and physic

211 eled standards was constructed, including 78 carbonyl metabolites with each containing MS, retention

212 databases with most of them belonging to the carbonyl metabolites.

213 le ligands, including van der Waals', ionic, carbonyl, metal, hydrophobic, and halogen bond contacts,

214 owed by reductive removal of the beta-lactam carbonyl moiety.

215 ng Br from CBrCl3 to the alpha-carbon of the carbonyl moiety.

216 mote CN group in the PivCN renders the PivCN carbonyl more electropositive and thus susceptible to nu

217 powerful method for accessing the beta-amino carbonyl motif that remains underdeveloped.

218 transit between N1-carbonyl symmetric and N1-carbonyl, N7-amino base-pairing arrangements.

219 aracterized by linear atom arrangement, with carbonyl O atom positioned on the three-fold symmetry ax

220 s found to form a key hydrogen bond with the carbonyl of Leu41 in the FXIa active site, resulting in

221 tures showed a hydrogen bond to the backbone carbonyl of Met-631.

222 acts as hydrogen bond donor for the backbone carbonyl of Pro1888.

223 ed on a novel coumarin scaffold in which the carbonyl of the lactone function of the original coumari

224 action between organic azides and the portal carbonyls of cucurbiturils.

225 gen bonds formed between water and the three carbonyls of TReF18.

226 the design principle of iron(III)-catalyzed carbonyl-olefin metathesis reactions.

227 s as reactive intermediates in the catalytic carbonyl-olefin ring-closing metathesis has been obtaine

228 Iron(III)-catalyzed carbonyl-olefin ring-closing metathesis represents a new

229 reductive coupling of alkenylpyridines with carbonyl or iminyl derivatives with the aid of a Lewis a

230 C)3 is more robust than Cr(0) complexes with carbonyl or monodentate isocyanides, manifesting in comp

231 irst-generation products of these reactions, carbonyl oxides (often named Criegee intermediates), is

232 Criegee intermediates are very reactive carbonyl oxides that are formed in reactions of unsatura

233 Addition of carbonyl oxygen at the alpha-position and formation of C

234 he peptide bond through interaction with the carbonyl oxygen atom.

235 mple nonredox substitution of the C2-uridine carbonyl oxygen by sulfur is catalyzed by tRNA thiouridi

236 entify an alpha-helical switch that shifts a carbonyl oxygen into the active site to coordinate a met

237 tease activity by movement of the equivalent carbonyl oxygen into the active site.

238 triple bond, and solid K3PO4 interacts with carbonyl oxygen, promoting intermolecular nucleophilic a

239 rol experiments established retention of the carbonyl oxygens in the enzymatic products during the tr

240 d activated olefin-derived nucleophiles with carbonyl partners.

241 lkenal-phenol reaction was characterized and carbonyl-phenol adducts were produced firstly by epoxide

242 l or slightly basic conditions and different carbonyl-phenol adducts were produced.

243 This is the first report showing that carbonyl-phenol reactions involving lipid-derived reacti

244 All these results suggest that carbonyl-phenol reactions may be used to modulate flavor

245 tor antagonist [N2-2-2-oxoazepan-3-yl amino] carbonyl phenyl benzo (b)thiophene-2-carboxamide (ANA-12

246 which we attribute to the larger size of the carbonyl portals of CB[8]; this suggests routes to devel

247 e hydroxyl group of Hzp and a backbone amide carbonyl positioned across the dimer interface may be re

248 of several substituted N-(pivaloyloxy)alkoxy-carbonyl prodrugs of 14 designed to circulate inert in p

249 nd Ph* (Me5C6) ketones to give beta-branched carbonyl products is described (21 examples).

250 ported in the literature invoke N-alkyl or N-carbonyl-protected sulfamidates.

251 (11)C-Carbonyl radiopharmaceuticals based on labeled carboxyli

252 mine to pyroglutamic acid, the typical amino-carbonyl reaction was slowed down.

253 ecently developed and commercially available carbonyl-reactive tandem mass tags (aminoxyTMT) enable m

254 anometallic reagents and discrete alcohol-to-carbonyl redox reactions are not required.

255 Carbonyl Reductase 1 (CBR1) is a ubiquitously expressed

256 (S)-carbonyl reductase II (SCRII) from Candida parapsilosis

257 n as ketoreductase can be transformed from a carbonyl reductase into an initiator of radical species

258 e-pot cascades with other enzymes, including carbonyl reductases (CREDs), hydrolases and monoamine ox

259 a(2+) binding to the PI(4,5)P2 headgroup and carbonyl regions leads to confined lipid headgroup tilti

260 Linear interaction NH3(+) - carbonyl represents an interesting example of ion-dipole

261 ish the starting pyruvate precursor from the carbonyl resonances in the resulting products, these pro

262 aryl(hetero)aryl halides using CHCl3 as the carbonyl source in the presence of KOH.

263 aliphatic aldehydes, including the reactive carbonyl species (RCS) acrolein, hydroxyl-2-nonenal, and

264 This study investigates the role of Reactive Carbonyl Species (RCS) from the Maillard reaction on bro

265 ealed that the elimination of toxic reactive carbonyl species during germination and seedling establi

266 al (MGO) and glyoxal (GO) are toxic reactive carbonyl species generated as by-products of glycolysis.

267 The influence of carbonyl species on the trigeminal burn of distilled spi

268 insertion of carbenes derived from silyl- or carbonyl-stabilized diazoalkanes into Au-C bonds at temp

269 g and aggregation was determined by inducing carbonyl stress in young mice, which recapitulated the i

270 al mol(-1) for BTP) include its high lactone carbonyl stretching energy (1821 cm(-1) in acetonitrile

271 n extended compilation of NBO charges and IR carbonyl stretching frequencies of various substituted b

272 ensional infrared (2D IR) spectroscopy, on a carbonyl stretching mode of tricarbonylchloro-9-octadecy

273 placed on the thermal evolution of the ester carbonyl stretching modes (1800-1700cm(-1)) and the comp

274 Analysis of the carbonyl stretching region for chlorophyll a excitations

275 By monitoring the dynamics of the ester carbonyl stretching vibration in hydrated phosphocholine

276 ing LC-MS is a useful tool for profiling the carbonyl submetabolome of complex samples with high cove

277 abeling (CIL) LC-MS method for profiling the carbonyl submetabolome with high coverage and high accur

278 Readily available beta-carbonyl-substituted aldehydes are shown to be exception

279 Hydroperoxy, hydroxyl and carbonyl-substituted CPA derivatives were tentatively id

280 olymers derived from the copolymerization of carbonyl sulfide (COS) and epoxides by metal-free Lewis

281 ase kinetics from a series of isomeric caged-carbonyl sulfide (COS) compounds, including thiocarbamat

282 Carbonyl sulfide (COS) is a gas that may play important

283 ntury that is based on long-term atmospheric carbonyl sulfide (COS) records, derived from ice-core, f

284 ical processes with variable contribution of carbonyl sulfide (OCS) shielding in an evolving volcanic

285 molation of benzyl thiocarbamates to release carbonyl sulfide, which is rapidly converted to H2S by c

286 s in non-nucleophilic substrates using alpha-carbonyl sulfoxonium ylides has not been so far investig

287 Carbonyl sulphide (COS) is a potential tracer of gross p

288 namic G:G base pairs that transit between N1-carbonyl symmetric and N1-carbonyl, N7-amino base-pairin

289 ophene-2,6-diyl][3-fluor o-2-[(2-ethylhexyl)-carbonyl]-thieno[3,4-b]thiophenediyl]]) thin films is in

290 ra methodology, was subjected to a reductive carbonyl transposition to afford 8-(4-methoxyphenyl)peri

291 use of phenolics, although the lipid-derived carbonyl trapping ability of phenolics is still poorly u

292 e (PYB) and two members of the sulfonylamino-carbonyl-triazolinone (SCT) herbicide families, revealin

293 lotris(ethane-2,1-diyl))tris(azanediyl))tris(carbonyl))tris(4-ox o-4H-pyran-3-olate) (Gd-TREN-MAM).

294 tile and useful reagent, mainly for reducing carbonyl-type substrates.

295 triggered by electron transfer to amide-type carbonyls, using SmI2 -H2 O, provide straightforward acc

296 Reactive carbonyls were derivatized with O-(biotinylcarbazoylmeth

297 Most carbonyls were derived from dicarbonyls (mainly glyoxal)

298 eral amino acids can be oxidized to reactive carbonyls, which are often used to monitor oxidative str

299 ssed by hydrogen bonding of the cis-aldehyde carbonyl with the DHAP enamine phosphate dianion through

300 the first reported [3+3]-cycloaddition of a carbonyl ylide.