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 -amide after the first amidation step of the diester.

4 ting from a commercially available glutamate diester.

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

6 koxide by TFAA to produce the nonsymmetrical diester.

7 protein revealed an unusual furanosyl borate diester.

8 rt-butylchloromethyl sulfide gave an achiral diester.

9 2) and an alpha,beta,gamma,delta-unsaturated diester.

10 gned to catalyze the hydrolysis of phosphate diesters.

11 quiv of the fatty acids gave the symmetrical diesters.

12 nates, and several polyfluoroalkyl phosphate diesters.

13 rolysis of phosphate monoesters or phosphate diesters.

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

15 bserved for solution hydrolysis of phosphate diesters.

16 of maleic acid diesters to give fumaric acid diesters.

17 istent with that previously proposed for DHP diesters.

18 ase that preferentially hydrolyzes phosphate diesters.

19 eries of substituted methyl phenyl phosphate diesters.

20 se (NPP), preferentially hydrolyze phosphate diesters.

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

22 nobenzil from four different p-cyanobenzoate diesters.

23 ed the corresponding polymer-bound phosphate diesters.

24 ificantly higher than those of the mono- and diesters.

25 ccessible alpha,beta,gamma,delta-unsaturated diesters.

26 ted into levels of exposure to six phthalate diesters.

27 of the clinical candidate BMS-986251, using diester 1 as a critical component.

28 Diester 1 is a novel chiral synthon useful in drug disco

29 ns of 1,6,7,12-tetrachloroperylene monoimide diester 1.

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

31 Mechanistic studies with a model diester, 1,2-ethanediol dibenzoate, suggest the reaction

32 synthetic route to differentially protected diester, 1-(tert-butyl) 4-methyl (1R,2S,4R)-2-methylcycl

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

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

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

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

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

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

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

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

41 the predominant products (~40%) followed by diesters (~33%), triesters (~9%) and trace amounts of te

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

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

44 2 FTOH and the 6:2 polyfluoroalkyl phosphate diester (6:2 diPAP) was quantified.

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

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

47 5 astaxanthin monoesters, and 10 astaxanthin diesters (7+/-1mg astaxanthin/g).

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

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

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

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

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

53 ected to cycloaddition with the cyclopropane diester afford a trouble-free formulation of the valued

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

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

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

65 titrated with various substrates, including diesters and diamides, via (1)H NMR spectroscopy and iso

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

67 rylsulfonate monoesters or charged phosphate diesters and fluorophosphates.

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

69 sed using this method, and several phthalate diesters and monoesters were successfully quantified.

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

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

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

73 Data for phthalate diesters and siloxanes suggest that volatility-dependent

74 for simultaneously extracting six phthalate diesters and six of their metabolites (phthalate monoest

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

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

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

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

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

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

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

82 Although phosphate diesters are cognate substrates for NPP but promiscuous

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

84 Fumaric acid diesters are important building blocks for organic synth

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

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

87 The resulting phosphorothioate diesters are then substantially desulfurized upon recurr

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

89 ns from above the aromatic rings with chiral diester arms.

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

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

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

93 ariety of complex molecules carrying sulfate diesters at various positions, including monosaccharides

94 tic nitration strategy operating with chiral diester auxiliaries, and it provides an enantioselective

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

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

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

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

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

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

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

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

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

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

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

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

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

108 3-monochloropropanediol (3-MCPD) fatty acid diesters can be produced.

109 1,2-Aromatic diesters can be transformed into strained bridged polycy

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

111 eduction of several aromatic and unsaturated diesters, can be efficiently and regioselectively alkyla

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

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

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

115 leaving group, rather than the isoelectronic diester complex.

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

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

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

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

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

121 ric hindrance in the side chains, or a rigid diester decreases the activities of prodrugs in comparis

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

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

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

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

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

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

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

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

130 lic activity toward both triester DEDNPP and diester EDNPP.

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

132 2,4-dinitrophenyl phosphate (DEDNPP) and the diester ethyl 2,4-dinitrophenyl phosphate (EDNPP) but re

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

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

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

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

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

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

139 Efficient sulfate diester formation was achieved through systematic optimi

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

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

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

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

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

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

146 The facile subsequent conversion of the diester groups into an imide group resulted in novel PBI

147 Phosphonate diester groups previously reported to form a covalent bo

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

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

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

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

152 ompeting vdW interactions do not allow H(2)O-diester H-bonding, thus forcing nBA side groups to adapt

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

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

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

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

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

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

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

160 Our calculations suggest that sulfate diester hydrolysis proceeds through loose transition sta

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

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

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

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

165 tabilizes the transition state for phosphate diester hydrolysis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 , particularly for the PFOS precursor SAmPAP diester (max 1 872 mug kg(-1)).

195 Building from phosphate monoesters to diesters may have enabled the synthesis of nucleic acids

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

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

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

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

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

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

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

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

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

207 omprises one Zn(II) ion to which a phosphate diester of DNA is coordinated.

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

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

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

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

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

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

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

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

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

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

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

219 Phosphorus monoester and diester organic species were dominant and present in abo

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

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

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

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

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

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

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

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

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

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

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

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

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

233 nserved domain family, the glycerophosphoryl diester phosphodiesterases.

234 yrophosphate (HMBP) as well as their aryloxy diester phosphonamidate prodrugs, termed ProPAgens.

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

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

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

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

239 Boranephosphonate diesters react with heteroaromatic and certain tertiary

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

241 thio-substitution on phosphate monoester and diester reactions.

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

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

244 11 Po species were detected in the mono- and diester region.

245 13-didecanoate, active and inactive, phorbol diesters, respectively.

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

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

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

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

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

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

252 0(2)-10(6), depending on the identity of the diester substrate.

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

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

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

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

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

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

259 948 reflecting the effects of bonding of the diester to the Co(III).

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

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

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

263 catalyzing the isomerization of maleic acid diesters to give fumaric acid diesters.

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

265 Data of seven 3-MCPD diesters together with corresponding total 3-MCPD equiva

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

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

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

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

270 ety, a vinyl group, a beta,gamma-unsaturated diester unit, and vicinal stereogenic centers in up to 6

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

272 The squarate diester used as an electrophile enabled sequential amida

273 of the alkaline hydrolysis of diaryl sulfate diesters, using different DFT functionals as well as mix

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

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

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

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

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

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

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

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

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

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

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

285 Phthalate diesters were found at concentrations of up to 982 ng g(

286 The highest levels of 3-MCPD diesters were found in palm oils, for 1,2-Dilinoleoyl-3-

287 1,4-Aromatic diesters were reductively dialkylated and then transform

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

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

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

291 from the reductive alkylation of a phthalate diester with hindered halides followed by rearomatizatio

292 00-fold at 25 degrees C) than expected for a diester with leaving groups of pK(a) 9.09.

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

294 d by a reaction of the resulting unsaturated diesters with Me(3)SnLi.

295 rolyses phosphonate monoesters and phosphate diesters with similar efficiency.

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

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

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

299 oval of the aryl masking groups from sulfate diesters yielded the corresponding O-sulfate products in

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