ライフサイエンスコーパス: diester

1 an anticipated degradation product of SAmPAP diester).

2 sulfated polysaccharides, oligomeric phospho-diesters).

3 te anion and for water attack on the neutral diester.

4 koxide by TFAA to produce the nonsymmetrical diester.

5 protein revealed an unusual furanosyl borate diester.

6 rt-butylchloromethyl sulfide gave an achiral diester.

7 -amide after the first amidation step of the diester.

8 rolysis of phosphate monoesters or phosphate diesters.

9 roups to olefins and access 1,1-cyclopropane diesters.

10 ted into levels of exposure to six phthalate diesters.

11 bserved for solution hydrolysis of phosphate diesters.

12 istent with that previously proposed for DHP diesters.

13 ase that preferentially hydrolyzes phosphate diesters.

14 eries of substituted methyl phenyl phosphate diesters.

15 se (NPP), preferentially hydrolyze phosphate diesters.

16 lter normal 3'-5' diesters to aberrant 2'-5' diesters.

17 nobenzil from four different p-cyanobenzoate diesters.

18 ed the corresponding polymer-bound phosphate diesters.

19 ble of efficiently uncovering phosphomannose diesters.

20 s of both phosphate monoesters and phosphate diesters.

21 ld also catalyze the hydrolysis of phosphate diesters.

22 rs are distinct from that of phosphoramidate diesters.

23 nity to inorganic phosphate and its mono- or diesters.

24 alysis of the chromogenic phosphate mono- or diesters.

25 gned to catalyze the hydrolysis of phosphate diesters.

26 quiv of the fatty acids gave the symmetrical diesters.

27 ysis of 8-L (L = solvent) to form the linear diester, 1,19-dimethylnonadecandioate, whereas 9 does no

28 ith sodium diethylmalonate in THF to produce diester 11, which after hydrolysis and cyclization affor

29 The easily isolated para diester (11) crystallized before the meta diester (12) f

30 to the formation of monoesters (e.g., 18) or diesters (11, 12), as needed, relying on the differentia

31 diastereoselective demethoxycarbonylation of diester 12 to form the trans-azetidinone 13.

32 ra diester (11) crystallized before the meta diester (12) from HOAc.

33 Homologation to diester 18 and ring formation by Dieckman cyclization, f

34 te salt 1-CO(2)()Na > triester 1-CO(2)()Et > diester 2-CO(2)()Et > monoester 3-CO(2)()Et) and may lea

35 s catalysts of the cleavage of the phosphate diester 2-hydroxypropyl-4-nitrophenyl phosphate (HPNP).

36 as follows: O,O-diethyl piperidinophosphate diester (2), O,O-diethyl phosphate (3), and O-ethyl 4-ni

37 of 2,6-azulenedicarboxylic acid (I) from its diester, 2-CO(2)(t)Bu-6-CO(2)-C(10)H(6) (II), is reporte

38 owed by esterification gave the cyclopropane diester 22, which upon hydrolysis gave cis-2-(2'-carboxy

39 While the dicarbamate was inactive, the diester (2cPE) behaves like a prodrug and is converted i

40 Treatment of scalemic diesters 4 with t-BuLi, followed by saponification in th

41 ate (3), and O-ethyl 4-nitrophenyl phosphate diester (4).

42 2 FTOH and the 6:2 polyfluoroalkyl phosphate diester (6:2 diPAP) was quantified.

43 e observed for 6:2 polyfluoroalkyl phosphate diester (6:2diPAP) as well as well-known PFASs such as p

44 component cascade coupling with chiral nitro diester 7, which is easily accessed via a highly enantio

45 5 astaxanthin monoesters, and 10 astaxanthin diesters (7+/-1mg astaxanthin/g).

46 e and S-p-bromobenzylglutathione cyclopentyl diester, a competitive inhibitor of glyoxalase I, result

47 synthesizing the 3,5-O-dicaffeoylquinic acid diester, a major constituent of the immature coffee grai

48 Stable phosphonate diester-Ab adducts were resolved by column chromatograph

49 omer sulfonates or polyfluoroalkyl phosphate diesters accounted for a relatively minor proportion of

50 ta) for chloride, bromide, iodide, phosphate diester, acetate, benzoate, perrhenate, nitrate, triflim

51 The small-molecule diesters act as diluents that increase the average dista

52 pon reduction with LiAlH4-Irradiation of the diesters afforded a 1:1 mixture of the heretofore unknow

53 under a CO atmosphere to give mainly acyclic diesters along with some acyclic chloro-substituted mono

54 glycans containing either phospho-mono- or -diesters although, like the CD-MPR, it differentially re

55 zed copolymerization of lactone with dialkyl diester and amino diol, and their hydrophobicity adjuste

56 e an accurate model of the neutral phosphate diester and does not provide information about a reactio

57 work, the biodegradation potential of SAmPAP diester and EtFOSE by bacteria in marine sediments was e

58 studies on ligands equipped with phosphonate diester and ether H-bond acceptors were inconclusive, bu

59 ite itself to discriminate between phosphate diester and monoester substrates.

60 .05) correlation was observed between SAmPAP diester and N-ethyl perfluorooctane sulfonamido acetate

61 cantly from the reaction of the noncomplexed diester and resembles the reactions of triesters.

62 ating from the (R,S/S,R) diastereomer of the diester and the exo-trans-exo, deriving from the (R,R/S,

63 alkaline hydrolysis of the phosphorothioate diester and triester exhibits somewhat less advanced bon

64 Addition of alpha,gamma-diesters and alpha-monoesters enhanced chemical stabilit

65 iety of 9-functionalized 1,8-diazaanthracene diesters and amino acids is described.

66 aper, we use a combination of nonsymmetrical diesters and computer modeling to identify that the remo

67 ive for cyclic 1,3-diesters over acyclic 1,3-diesters and esters.

68 l alkoxyalkyl acyclic nucleoside phosphonate diesters and identified octadecyloxyethyl benzyl 9-[(2-p

69 ts for NPP-catalyzed hydrolysis of phosphate diesters and monoesters.

70 of the monoesters while slowing the rates of diesters and of triesters.

71 on at the phosphorus center of H-phosphonate diesters and oxazaphospholidine oxides.

72 ook advantage of the easily separated benzyl diesters and their derived acid chlorides (19, 21), with

73 rins (e.g., bearing alkyl/ester, aryl/ester, diester, and no substituents) in a few days from commerc

74 reported for analogous phosphate monoester, diester, and triester reactions.

75 ulations of 6-O-monoesters, symmetrical 6,6'-diesters, and 2,6,6'-triesters of fatty acids were calcu

76 of phosphorothioate diesters, H-phosphonate diesters, and oxazaphospholidine oxides were determined.

77 Pyromellitate triesters afforded the ortho diester anhydrides upon distillation, thereby providing

78 epared by the reaction between a phosphonate diester anion and a P(III) chlorophosphine, or its P(V)

79 Although phosphate diesters are cognate substrates for NPP but promiscuous

80 the reported studies of reactions of sulfate diesters are for dialkyl or alkyl aryl diesters, which u

81 with the enzyme and why neutral phosphonate diesters are more potent inhibitors than monoanionic pho

82 thyl (9), and diphenyl (10) phosphonoformate diesters are substantially accelerated by Ce(IV), Th(IV)

83 The resulting phosphorothioate diesters are then substantially desulfurized upon recurr

84 Phthalate diesters are used extensively in a variety of consumer p

85 secrete acid hydrolases with phosphomannose diesters as a consequence of the deficient UCE activity.

86 tative series of 2-(het)arylcyclopropane-1,1-diesters as well as donor-acceptor cyclopropanes with ot

87 stabilize the anionic guanosine-borate (GB) diesters, as well as the G4-quartets.

88 s glycoprotein (gp) 120 with the phosphonate diester at the C terminus formed covalent adducts with s

89 VIP containing an electrophilic phosphonate diester at the Lys(20) residue.

90 n and quantification of the furanosyl borate diester (BAI-2) subclass of autoinducer 2 (AI-2), QS mol

91 e during the catalytic activation of the MeP diester bond.

92 r-343) to cause direct hydrolysis of the MeP diester bond.

93 nt to hydrolyse rhamnogalacturonan II borate diester bonds neither affected chains length or branchin

94 are also linked by the A rings by an alkenyl diester bridge to restrict the conformational flexibilit

95 uronan-II (RG-II) is cross-linked via borate diester bridges, which influence the expansion, thicknes

96 unctionalized to the desired C21 alpha,omega-diester building block with a linear selectivity of over

97 reversible binding of the hapten phosphonate diester by polyclonal IgG from mice immunized with gp120

98 ersible binding of a biotinyated phosphonate diester by the IgG and Fv preparations was observed, con

99 Increased total organic P and orthophosphate diesters by P NMR and accumulated inositol hexaphosphate

100 ntioenriched beta-substituted alpha-keto-1,5-diesters by using the hydrazone moiety as a masked carbo

101 tes served as regiospecific sources of other diesters, by further esterification followed by hydrogen

102 the palmitate (C16), the octadecyl glutarate diester (C18-C5) and the decyl carbamate (CB10).

103 Squaric acid diesters can be applied as reagents to couple two amino-

104 o demonstrated that racemic cyclopropane 1,1-diesters can undergo dynamic kinetic asymmetric annulati

105 sed the preferential phosphate monoester and diester catalysis of PafA and NPP, respectively.

106 igher proportion of carotenoid monoesters to diesters compared to ripe fruits were observed.

107 amounts of organic P such as monoesters and diesters, compared to the other two sites, but that thes

108 leaving group, rather than the isoelectronic diester complex.

109 ate to high yielding and affords alpha-silyl diesters, compounds that previously have not been readil

110 SAmPAP diester concentrations in sediment (40-200 pg/g dry weig

111 as inhibited by an electrophilic phosphonate diester, consistent with a nucleophilic catalytic mechan

112 methyl demeton-S is due to the presence of a diester contaminant in the commercial material.

113 Specifically, a diester cryptand with a pyridyl nitrogen atom located at

114 ies of N-S-blocked glutathione monoester and diester derivatives based on N-benzyloxycarbonyl-S-(2,4-

115 a-lap prodrug nanotherapeutics consisting of diester derivatives of beta-lap encapsulated in biocompa

116 Compared to the parent drug, diester derivatives of beta-lap showed higher drug loadi

117 Among symmetrical diester derivatives, the optimal antagonist potency occu

118 esters (WEs), cholesteryl esters (CEs), and diesters (DEs) were corrected for peak overlapping and i

119 A hapten phosphonate diester devoid of gp120 inhibited the catalytic activity

120 ical strategy dedicated to 4 major phthalate diesters (DiBP, DnBP, BBzP and DEHP) monitoring in food

121 termediates of PTA and its equally important diester, dimethyl terephthalate (DMT).

122 s, including polyfluoroalkyl phosphoric acid diesters (diPAP), perfluorophosphonates (PFPA), and perf

123 FCAs), such as the polyfluoroalkyl phosphate diesters (diPAPs), which have been detected in WWTP and

124 rsors and 11 polyfluoroalkyl phosphoric acid diesters (diPAPs).

125 h carboxy-fluorescein diacetate succinimidyl diester dye to enable high-resolution tracking of cell d

126 lic activity toward both triester DEDNPP and diester EDNPP.

127 first examples of ansa-zirconocene mono- and diester enolate complexes: rac-(EBI)ZrMe[OC(O(i)Pr)=CMe(

128 2,4-dinitrophenyl phosphate (DEDNPP) and the diester ethyl 2,4-dinitrophenyl phosphate (EDNPP) but re

129 s of the monoanion and dianion of pNPPT, the diester ethyl pNPPT, and the triester dimethyl pNPPT was

130 For the diester, ethyl p-nitrophenyl phosphate, the nonbridge 18

131 ctivation parameters measured herein for the diesters, ethyl p-nitrophenyl phosphate and ethyl p-nitr

132 mg/kg IP bromobenzyl-glutathione cyclopentyl diester every second day), was able to increase vascular

133 e secreted hydrolases contained GlcNAc-P-Man diesters, exhibited a decreased affinity for the cation-

134 of this photoproduct to a spirocyclic amido diester followed by enzymatic desymmetrization produces

135 Low-molecular weight (LMW) phthalate diesters function as plasticizers, fixatives or solvents

136 gated donor substituent vicinal to a malonyl diester group undergo cycloadditions with diverse conjug

137 s inhibited by VIP devoid of the phosphonate diester group.

138 antigens containing biotinylated phosphonate diester groups (covalently reactive antigen analogs, CRA

139 d to investigate the role of the 3,3-geminal diester groups and the origin of torquoselectivity in th

140 rmal growth factor receptor with phosphonate diester groups at Lys side chains and a synthetic peptid

141 Phosphonate diester groups previously reported to form a covalent bo

142 hetic gp120-(421- 436) devoid of phosphonate diester groups, respectively.

143 ct mutational events at a cytosine-phosphate diester-guanidine dinucleotide mutation hot spot.

144 ine methylation of DNA at cytosine-phosphate diester-guanine dinucleotides, histone modifications, mi

145 alue of EM for an intramolecular phosphonate diester H-bond is about 4 times lower than the correspon

146 absolute configurations of phosphorothioate diesters, H-phosphonate diesters, and oxazaphospholidine

147 This versatile amino diester has been previously used to synthesize amino-dif

148 tion on the solvolytic behavior of carbonate diesters has been investigated kinetically by applying t

149 te diester orientations and phosphorothioate diesters highlight that the interpretation of thio-subst

150 AP accelerates the rate of phosphate diester hydrolysis by 10(11)-fold relative to the rate o

151 ely 10(11)-fold for both phosphate mono- and diester hydrolysis by each enzyme indicated that the Zn(

152 NPP preferentially catalyzes diester hydrolysis by factors of 10(2)-10(6), depending

153 the role of metal ion cofactors in phosphate diester hydrolysis catalysed by a flap endonuclease has

154 e associative transition state for phosphate diester hydrolysis in solution.

155 transition state for AP-catalyzed phosphate diester hydrolysis is indistinguishable from that in sol

156 environment alters the transition state for diester hydrolysis to be looser in its bonding to the in

157 the reaction and the chemistry of phosphate diester hydrolysis were assigned unequivocally using mas

158 as minimal effect on the rate of spontaneous diester hydrolysis, in striking contrast to the major ef

159 te that could lead to preferential phosphate diester hydrolysis, we have determined the structure of

160 tabilizes the transition state for phosphate diester hydrolysis.

161 me on the environmental occurrence of SAmPAP diester in marine sediments from an urbanized marine har

162 of EtFOSE and recalcitrant nature of SAmPAP diester in part explains the elevated concentrations of

163 Placement of the scissile phosphate diester in the active site required the presence of diva

164 sium ion interacts directly with a phosphate diester in the substrate DNA.

165 tion was the use of an iodocinnabarinic acid diester in which the amino group was masked with two Boc

166 oesters react modestly faster than phosphate diesters in model reactions, a similarly modest stimulat

167 gent KHSO(5), prepared easily from Oxone, to diesters in one simple transformation.

168 rgy surfaces for the hydrolysis of phosphate diesters in solution, with a variety of leaving groups.

169 ferent fatty acids to give nonsymmetric 6,6'-diesters in very good yields.

170 s the EtFOSE-based phosphate diester (SAmPAP diester) in any environmental compartment.

171 ainst S-p-bromobenzylglutathione cyclopentyl diester-induced apoptosis under high glucose conditions.

172 aloyl derivative, a representative uncharged diester, inhibited ADP-induced aggregation in both rat (

173 glycol through a bis(hydroxypropyl) fumarate diester intermediate.

174 te, whereas 9 does not react and no branched diester is observed.

175 nium units toward the cleavage of phosphoric diesters is deeply investigated both with kinetic experi

176 alcohol, the usual mixture of meta and para diesters is obtained, separated by crystallization from

177 rapid access to gamma-substituted propyl-1,1-diesters, ketoesters, cyanoesters, cyanoamides, dinitril

178 y: L-phenylalanyl-adenosine-5'-monophosphate diester (L-Phe-AMP), L-Phe-S-4'-phosphopantetheine(Ppant

179 nd L-phenylalanyl-adenosine-5'-monophosphate diester (L-Phe-AMP), transferring it to the HS-phosphopa

180 l H-bonds in toluene, so for the phosphonate diester ligand system, 23 of the 24 supramolecular archi

181 her ligands, and KEM > 1 for the phosphonate diester ligands.

182 The first site is the scissile phosphate diester linkage and nucleotides downstream of this and t

183 was not observed for the scissile phosphate diester linkage implying that electrophilic catalysis by

184 5 (ggGGTCAACGTTGAgggggG, with g representing diester linkages and phosphorothioate linkages being to

185 ically catalyses the hydrolysis of phosphate diester linkages contained within the RNA portion of DNA

186 osphorothioate replaces one of the phosphate diester linkages.

187 Our efforts led to the discovery of diester-linked conjugates that, upon in vivo hydrolysis,

188 uicycline C-glycoside tethered by a tetraene diester linker to an aminocoumarin.

189 at lead molecule 30, bearing a biodegradable diester linker, formed small complexes with nucleic acid

190 2c was conjugated to PEG via dicarbamate and diester linkers.

191 idylcholine (DPPC), a conventional monopolar diester lipid.

192 se transitions of saturated diacyl monopolar diester lipids.

193 -O-palmitate, lutein 3-O-palmitate) and four diesters (lutein dilinoleate, lutein 3'-O-linoleate-3-O-

194 alyzed intramolecular photocycloadditions of diesters made of endo-dicyclopentadiene derivatives link

195 The key feature of the squaric acid diester mediated coupling is the reduced reactivity of t

196 verview of the well-established squaric acid diester mediated coupling reactions for glycoconjugates

197 dants (OPFRs) and plasticizers and their two diester metabolites were investigated in a wastewater tr

198 Previously, the metal complex of the diester methyl-p-nitrophenyl phosphate was found to hydr

199 spholane-2-sulfide), which gave rise to O,O'-diester-methylenediphosphonotetrathioate analogues 1a-k

200 to nitro-olefins and alpha,beta-unsaturated diesters (Michael-type reactions) have also been develop

201 21-431 with a C-terminal amidino phosphonate diester mimetic of the Lys(432)-Ala(433) bond was employ

202 leobases or desulfurize the phosphorothioate diester model to an appreciable extent.

203 es and do not desulfurize a phosphorothioate diester model under conditions mimicking large-scale oli

204 h a reduction in sebaceous gland lipids (wax diesters/monoesters, sterol esters).

205 erylene tetraester and a 1,7-dibromoperylene diester monoimid.

206 work, we study the hydrolysis of a phosphate diester, MpNPP(-), in solution, two experimentally well-

207 to polycyclic musk odorants or a macrocyclic diester musk odorant.

208 ss I was represented by three isomers of the diester of 5alpha-cholestane-3,17-diol with 5-(4'-carbox

209 Analysis of the 3',5'-phosphate diester of the monomeric lesion released from single dia

210 an oxygen atom on the penultimate phosphate diester of the primer strand.

211 verall selectivity to the linear alpha,omega-diester of up to 75%.

212 First, we prepared nonsymmetrical diesters of (+/-)-1 using another regioselective, but no

213 es of cyclitol derivatives, namely mono- and diesters of 1,2:5,6-di-O-isopropylidene-myo-inositol and

214 enantioselective catalyst for hydrolysis of diesters of 1.

215 a and CriticalSorb(TM) (polyglycol mono- and diesters of 12-hydroxystearate (70%), polyethylene glyco

216 t] The electrochemical reduction of benzoate diesters of glycols has been studied in acetonitrile and

217 Hexano- and dodecano-tethered diesters of rhodamine B were prepared.

218 n surfaces via hexaethylene glycol phosphate diester oligomer spacers (0, 1, 2, 6 oligomers) was foun

219 unpairing that places the scissile phosphate diester on active site divalent metal ions.

220 aphospholidine oxide which forms a phosphate diester only when a 2-pyridyl TPG is applied.

221 trapeptide, a phosphotyrosine residue, and a diester or a diamide group, we find that, regardless of

222 These results imply that the diester or diamide derivatives of the d-tetrapeptides se

223 ic were prepared by using either adipic acid diester or diethyl squarate linkers.

224 propionates of ZnMb by formation of the heme diester or, for the first time, the diamide increases th

225 ly, our calculations for different phosphate diester orientations and phosphorothioate diesters highl

226 e reagent system is selective for cyclic 1,3-diesters over acyclic 1,3-diesters and esters.

227 Acceleration of H-phosphonate diester oxidation with iodine accompanied by a thermolab

228 labile Po, followed by labile monoester- and diester-P.

229 bitors (S-bromobenzylglutathione cyclopentyl diester (pBBG) or methyl-gerfelin (MeGFN)) reduced immob

230 p-Methoxycinnamic diester (PCO-C) was identified, which has a crystalline,

231 Intermolecular phosphonate diester-phenol H-bonds are 2 orders of magnitude stronge

232 interactions were compared with phosphonate diester-phenol interactions in a closely related ligand

233 of the ribose O2' oxygen on the neighboring diester phosphate bond, and both reach the same product

234 (31)P relaxation of the diester phosphate of phospholipids in unilamellar vesicl

235 and higher negative charge compared with the diester phosphates of most other phospholipids.

236 olism, GdpD (which denotes glycerophosphoryl diester phosphodiesterase) and Cls (which denotes cardio

237 subfamily VI); At4g26690 (glycerophosphoryl diester phosphodiesterase-like GPI-anchored protein); At

238 nserved domain family, the glycerophosphoryl diester phosphodiesterases.

239 e nitration procedure for perylene monoimide diesters (PMIDE) enables the synthesis of 1-nitro-PMIDE

240 ioselective formation of the monoacid from a diester precursor proceeds via a novel fluoride-mediated

241 s indicate one CO is inserted in forming the diester product so the second ester group must arise fro

242 the menthyl (11a, 11b) or bornyl (11f) para diesters, prototypes of what promises to be a large clas

243 a carboxylic acid, produces a nonsymmetrical diester, RCO(2)(CH(2))(4)O(CH(2))(4)OCOCF(3), in high yi

244 e synchronous ones previously calculated for diester reactions in the same AP enzymes.

245 thio-substitution on phosphate monoester and diester reactions.

246 s studies, revealed the residues involved in diester recognition, including Y679.

247 ypothesize that the hydrophobicity of SAmPAP diester reduces its bioavailability, thus limiting biotr

248 11 Po species were detected in the mono- and diester region.

249 13-didecanoate, active and inactive, phorbol diesters, respectively.

250 Sulfuryl transfer reactions of sulfate diesters (RO-SO(2)-OR') proceeding by attack at sulfur h

251 , and sulfone groups replacing the phosphate diesters (S-DNAs) were synthesized from building blocks

252 ubstances such as the EtFOSE-based phosphate diester (SAmPAP diester) in any environmental compartmen

253 orooctane sulfonamidoethanol based phosphate diester (SAmPAP) is a potential perfluorooctanesulfonate

254 r the pH-independent hydrolysis of phosphate diesters, several kinetically equivalent mechanisms are

255 The observation that carbonate diesters solvolyze faster than the corresponding carboxy

256 and co-workers, who suggested that the same diester substrate goes through a much looser transition

257 0(2)-10(6), depending on the identity of the diester substrate.

258 oficiency for the most similar monoester and diester substrates in the two enzymes.

259 ts (KIEs) for a range of phosphate mono- and diester substrates.

260 The bound ligand is a furanosyl borate diester that bears no resemblance to previously characte

261 -catalyzed reaction of an alpha-diazo indolo diester that contains a tethered oxa-pentenyl side chain

262 monohydrolysis of a series of near-symmetric diesters that possess an exo-ester group and an endo-est

263 Acylation gave nonsymmetrical diesters that varied at the 4'-position.

264 the nitro group, and (for the monoester and diester) the secondary oxygen-18 isotope effect ((18)k(n

265 ilar H-bond strengths (amide and phosphonate diester), there is little correlation between the values

266 d of duplex to permit the scissile phosphate diester to contact catalytic divalent metal ions.

267 948 reflecting the effects of bonding of the diester to the Co(III).

268 ation, and finally conversion of the sulfate diester to the desired sodium salt.

269 SmI(2)-H(2)O reduces cyclic 1,3-diesters to 3-hydroxyacids with no over-reduction.

270 tions, bond migration may alter normal 3'-5' diesters to aberrant 2'-5' diesters.

271 The conversion of gem-diesters to chiral esters by the substitution reaction i

272 c transformation of racemic 1,1-cyclopropane diesters to prepare enantioenriched tetrahydrofuran (THF

273 An alternative synthesis of specific diesters took advantage of the easily separated benzyl d

274 nucleosides or with a model phosphorothioate diester under conditions approximating those of large-sc

275 showed higher proportions of orthophosphate diesters under paddy than under non-paddy management, li

276 Here we report that boranephosphonate diesters undergo facile nucleophilic substitution in a s

277 ibution, the relative stereochemistry of the diester units along the polymer chain, and ultimately th

278 The squarate diester used as an electrophile enabled sequential amida

279 bridging positions leads to cleavage of the diester via formation of a cyclic intermediate, but with

280 lent adducts of a hapten amidino phosphonate diester was attributed to micro and kappa/lambda subunit

281 In contrast, SAmPAP diester was highly recalcitrant to microbial degradation

282 Although SAmPAP diester was not detected in water, PFOS was observed at

283 The alkaline hydrolysis of diaryl sulfate diesters was shown to obey first-order kinetics with res

284 turbations in mass spectrometric profiles of diester wax and cholesteryl ester species.

285 se mice contained a reduced level of type II diester wax, a major mouse sebum lipid species, and show

286 ely, cholesterol, triacylglycerols, 1,2-diol diesters, wax esters, cholesteryl esters, and hydrocarbo

287 hydrolysis of either phosphate monoesters or diesters, we have measured a promiscuous sulfatase activ

288 n-6-one (5), and related cis-diols mono- and diesters were designed and synthesized.

289 bility of cinnamic esters from carnauba wax, diesters were extracted from carnauba wax powder.

290 myristic and palmitic acid as monoesters or diesters, were found.

291 s, cholesteryl esters, triacylglycerols, and diesters, whereas in negative mode, the major peaks dete

292 lfate diesters are for dialkyl or alkyl aryl diesters, which undergo reaction by carbon-oxygen bond f

293 The autoinducer AI-2 is a furanosyl borate diester whose synthesis depends on the enzyme LuxS.

294 00-fold at 25 degrees C) than expected for a diester with leaving groups of pK(a) 9.09.

295 The desymmetrization of prochiral diesters with a chiral phosphoric acid catalyst to produ

296 rolyses phosphonate monoesters and phosphate diesters with similar efficiency.

297 hydrolysis mechanism followed by uncomplexed diesters with the p-nitrophenolate leaving group.

298 drolysis of 4NPMP that is similar to that of diesters with the same leaving group.

299 The formation of lutein diesters, with greater stability, explains the slower ca

300 Diester ZnPorOMe(2) (2b) was made of a Zn(II) 5,10,15,20