ライフサイエンスコーパス: ester

1 rkup allows isolation of the pinacol boronic ester.

2 thase with N(omega) -nitro-l-arginine methyl ester.

3 an E-gamma-substituted boronic acid pinacol ester.

4 9) with IRDye 650 N-hydroxysuccinimide (NHS) ester.

5 m the allylic phosphate and the glycine aryl ester.

6 decyl ester>dodecyl ester>hexyl ester>methyl ester.

7 ene derivatives, with maleimides and maleate esters.

8 eased the changes in the safranal and crocin esters.

9 good ability to produce a large diversity of esters.

10 uced ho-trienol, beta-damascenone, acids and esters.

11 y affected by the presence of selected ethyl esters.

12 abeling of more than 50 (hetero)aryl boronic esters.

13 a-(1'-fluoro)-beta-(tributylstannyl)vinyl AA-esters.

14 noids and 11 were apocarotenoids fatty acids esters.

15 removal, as recently demonstrated for ethyl esters.

16 otal carnitine (P < 0.001) and all carnitine esters.

17 ation of benzylic C-H bonds with arylboronic esters.

18 ups, such as alkyl/aryl halides, azides, and esters.

19 rresponding alpha-hydroxy-beta,gamma-diamino esters.

20 ose carbons to triglycerides and cholesterol esters.

21 nthesize novel non-proteinogenic alpha-amino esters.

22 of haloarenes directly to boronic acids and esters.

23 omers in the case of alpha,beta-dialkylvinyl esters.

24 alyzed reaction of cyclopropanols with diazo esters.

25 and 12, as well as seco-mandelalide A methyl ester (13), have now facilitated mechanism of action and

26 Isopropyloxycarbonyloxymethyl (POC) ester 30 was the only prodrug that achieved substantial

27 grade oils in EVOO was 2% when using 3-MCPD esters, 5% for 2-MCPD esters, and 13-14% for GEs based o

28 derived 2-methyl-3-hydroxypentanoate methyl esters (8) by chiral GC-MS established that the BonMT2-c

29 luding 10 phenols, 25 alcohols, 11 acids, 39 esters, 8 hydrocarbons, 14 carbonyl compounds, 17 terpen

30 nnamic acid (36.4%), p-coumaric acid glucose ester (9.2%) and 1-O-beta-d-glucopyranosyl sinapate (5.6

31 amine-mediated glycosylation of the boronic ester, a variety of selectively protected di- and trisac

32 egulation of CsAOG, involved in ABA glycosyl ester (ABAGE) synthesis, and to a moderate induction of

33 nent, and gamma-amino-alpha,beta-unsaturated esters acting as a three-atom component to construct ind

34 the formation of a substrate-derived boronic ester alters the course of the reaction by selective pro

35 ive methods for the synthesis of ketones and esters, among others.

36 mpounds (dimethyl sulfide, ethanethiol), and ester and alcohol compounds associated with distinct 'su

37 c acids were prepared by deprotection of the ester and amide groups of ortho-benzoxylated cyclic benz

38 ing from a readily available indole-2-acetic ester and an alpha,beta-unsaturated N-sulfonyllactam.

39 The introduction of ester and carboxylate functionalities at the bay region

40 ciated with lower levels of mycolic acid wax ester and long-chain triacylglycerols than those for wil

41 nolics like thymol, quinicquinic-caffeicacid ester and polar dicaffeoylquinic acid; whereas higher li

42 the zwitterionic compounds with hydrocarbon ester and tertiary amine groups, the bulk polymer itself

43 s been achieved with a variety of amino acid esters and 2- or 4-vinylpyridine.

44 The resulting flavour profiles, including 36 esters and 6 alcohols compounds, were statistically eval

45 ho-Lithiated benzylamines react with boronic esters and a N-activator to afford ortho-substituted ben

46 ly accessible N,N-disubstituted glycine aryl esters and allylic phosphates.

47 Enoldiazo esters and amides have proven to be versatile reagents f

48 system enabled a wide range of alkyl boronic esters and aryl or alkyl boronic acids to react with ele

49 Recombinant PfPARE hydrolyses pepstatin esters and de-esterifies MMV011438.

50 (-/-) mice had less accumulation of retinyl esters and dysregulation of a striking array of genes, i

51 s, e.g., amino acids, organic acids, choline esters and glucose.

52 1,3-dipolar cycloaddition (1,3-DC) of imino esters and nitroalkenes, with alpha,beta-unsaturated ald

53 triterpene acids/esters, fatty alcohols, wax esters and phenols (lignans, tyrosol, hydroxytyrosol, ol

54 applications of the reactions of alpha-imino esters and related compounds in organic synthesis, cover

55 ) from a variety of arylboronic acid pinacol esters and substituted o-allylbenzamides.

56 pulcherrima produced higher concentration of esters and total volatile compounds.

57 ion and storage of oxidized LDL, cholesteryl esters and triglycerides were abolished in Hilpda cKO ma

58 The effect of cold plasma on crocin esters and volatile oils of saffron was studied for the

59 Glucose esters' and commercial sucrose esters' functionality as

60 enabled rapid synthesis of acrylate ketone, ester, and amide analogs.

61 tor increased the levels of TAG, cholesteryl ester, and RE in both rat and mouse HSCs.

62 6)-Carboxyfluorescein Diacetate Succinimidyl Ester, and size exclusion chromatography to remove uncon

63 functions such as vinyl-sulfones, -ketones, -esters, and -nitriles.

64 s 2% when using 3-MCPD esters, 5% for 2-MCPD esters, and 13-14% for GEs based on calculations of virt

65 ration of alpha-quaternary carboxylic acids, esters, and amides with a high degree of enantioselectiv

66 e of substrates, including organophosphates, esters, and carbonates.

67 holine-lipid species and gaining cholesteryl esters, and proteomic changes, with losses in cardioprot

68 taining triacylglycerols (TAGs), cholesteryl esters, and retinyl esters (REs).

69 ransformed into sodium sulfonates, sulfonate esters, and sulfonamides, as well as styrenes by Julia-t

70 triacylglycerols, phospholipids, cholesteryl esters, and wax esters in OG-treated sebocytes.

71 Especially the MCPD esters appear very specific and promising for the detect

72 These esters are apparently important markers of LAB esterase

73 Due to the adjacent ester group, alpha-imino esters are more reactive relative to other types of imin

74 Lutein esters are more stable than free lutein during post-harv

75 alpha-Imino esters are useful precursors for the synthesis of a vari

76 Esters are valuable electrophiles for cross-coupling due

77 cterized by a high production of unsaturated esters arising from partial catabolism of branched chain

78 a wide range of functional groups, including esters, aryl halides, aryl boronic esters, sulfonamides,

79 zylic isomers, when combined with a Hantzsch ester as the reductant.

80 porter gene defects, and validate riboflavin esters as a potential therapeutic strategy.

81 eap and easily prepared N-hydroxyphthalimide esters as aryl radical precursors and does not require t

82 However, the contents of volatile esters, associated to fruity flavor, were always higher

83 whereas it is suppressed following amide-to-ester backbone substitutions at Gly77 and Tyr78, even th

84 e show that stolonidiol binds to the phorbol ester binding site of protein kinase C (PKC), induces tr

85 e glycerophospholipids (PE, PS, and PC), via ester bond cleavage.

86 on by ALP, but CES-catalyzed cleavage of the ester bond on the molecules results in disassembly of th

87 10 of this motif auto-catalytically forms an ester bond with the heme 5-methyl, and the immobilized G

88 ally mediated by an unusual heme-polypeptide ester bond.

89 drophilic PGMA chains to form phenylboronate ester bonds in mildly alkaline aqueous solution (pH appr

90 r developmental stages in both forms, mainly ester-bound in the lignan macromolecule and slightly in

91 igosaccharides from benchtop stable anomeric ester building blocks becomes possible under mild reacti

92 inase C regulator, and plant-derived phorbol esters, but each ligand induces different activities.

93 6%), cyclosporine by 30 (7.7%), fumaric acid esters by 19 (4.9%), and more than 1 medication was used

94 alently reactive boronic acid pinacol (BPin) esters by kinetic discrimination during transmetallation

95 (C6F5)2 (7b), as well as the related boronic ester C14H8O2B(C6F5) (2).

96 locking was observed with rhodamine 19 butyl ester (C4R1), whereas the octyl ester (C8R1) was of poor

97 ine 19 butyl ester (C4R1), whereas the octyl ester (C8R1) was of poor effect.

98 t the natural product caffeic acid phenethyl ester (CAPE) disrupts neural crest gene expression, migr

99 allyl Pd intermediates, derived from allylic ester carbonates and palladium(0) catalyst, were found t

100 In the ester carbonyl band, the effect of changing temperature

101 hasis placed on the thermal evolution of the ester carbonyl stretching modes (1800-1700cm(-1)) and th

102 By monitoring the dynamics of the ester carbonyl stretching vibration in hydrated phosphoc

103 e high density lipoprotein (HDL)-cholesteryl ester (CE) uptake, mediated by scavenger receptor class

104 ses)].Baseline concentrations of cholesterol esters (CEs) were inversely associated with CVD.

105 alcohol levels and around twenty times more esters compared to L04.

106 Due to the labile ester containing link, this prodrug is converted back in

107 noleptic defects for samples with high alkyl esters content.

108 lic acyl azolium, opening to the aldehyde-to-ester conversion.

109 nitrate (ONO2) > carbonyl (CO) approximately ester (COO) > methylene (CH2).

110 in response to esterases due to an embedded ester cross-linker in the particle's core.

111 evaluation of the reactivity of the dimethyl ester derivative with various primary amines, this metho

112 Ester derivatives of the compounds 1 (X80), 22, and 24 d

113 rmed using diphenylborinic acid 2-aminoethyl ester (DPBA) as inducer of regioselectivity.

114 thiodipropionic acid di(N-hydroxysuccinimide ester (DTSP) as a self-assembled monolayer (SAM) agent.

115 ioaccessibility (17-42%) compared to sucrose ester emulsions (33-52% and 9-27%, respectively).

116 rospheres made of a higher molecular weight, ester end-capped PLGA displayed an osmotically induced/p

117 responds to the plant volatile compound pear ester ethyl-(E,Z)-2,4-decadienoate, while CpomOR6a respo

118 lso set specific limits for fatty-acid ethyl esters (FAEEs).

119 PHP wine contained the highest amounts of esters, fatty acids and anthocyanins, and the lowest con

120 groups, squalene, sterols, triterpene acids/esters, fatty alcohols, wax esters and phenols (lignans,

121 d through activation of the aryldiazoacetate ester for arylpropargyl cation dissociation followed by

122 ts have highlighted the potential of boronic ester formation as a bioorthogonal click reaction betwee

123 nalized examples bearing aldehydes, ketones, esters, free phenols, and heterocycles.

124 access densely functionalized alkyl boronate esters from abundant carboxylic substituents.

125 uiterpenoids, diterpenes alcohols, and sugar esters from trichomes of the plants, and recently charac

126 or the asymmetric synthesis of alkyl boronic esters, from the seminal hydroboration methods of H.

127 In particular, the synthesis of an ester-functionalised Ar-BIAN ligand was carried out by a

128 hain, an alicyclic ring, hydroxy, ether, and ester functionality, which offer the N-alkenylated produ

129 Glucose esters' and commercial sucrose esters' functionality as emulsifiers were compared.

130 Complexes of an ester-functionalized ligand were taken up by bacteria in

131 a process yield of 0.27 g-fatty acid methyl esters/g-glucose, which constitutes a 25% improvement ov

132 diamino and alpha-hydroxy-beta,gamma-diamino esters gave the protected forms of the 3-deoxy-3-aminosp

133 r each frying cycle were analyzed for 3-MCPD esters, GEs, free fatty acid (FFA) contents, specific ex

134 earomatization occurs with neopentyl boronic esters, giving the coupled products.

135 Due to the adjacent ester group, alpha-imino esters are more reactive relati

136 posed of a pyrene and a reactive succinimide ester group, interacts with graphene non-covalently via

137 , intramolecular trapping by the neighboring ester group, subsequent hydrolysis, and loss of methanol

138 r branched at the alpha-carbon) and aromatic ester groups have been synthesized, their solid-state st

139 rogen bonds, which alter the dynamics of the ester groups.

140 xist whether or not water interacts with the ester groups; however, water does accelerate the time-sc

141 hyl ester>hexyl esterdodecyl ester>octadecyl ester>BHT while the order for the BCB anti-oxidative act

142 B anti-oxidative activity was; BHT>octadecyl ester>dodecyl ester>hexyl ester>methyl ester.

143 ve activity was; BHT>octadecyl ester>dodecyl ester>hexyl ester>methyl ester.

144 compounds was in the following order: methyl ester>hexyl esterdodecyl ester>octadecyl ester>BHT while

145 was; BHT>octadecyl ester>dodecyl ester>hexyl ester>methyl ester.

146 owing order: methyl ester>hexyl esterdodecyl ester>octadecyl ester>BHT while the order for the BCB an

147 All sorbitan esters had little effect on polymorphism, whereas canola

148 rubinal and Apo-10'-zeaxanthinals fatty acid esters had not been previously tentatively identified in

149 olyketide natural product zincophorin methyl ester has attracted significant attention from synthetic

150 d active hexafluoroisopropyl (HFIP) benzoate esters has been developed.

151 ryl, heteroaryl, and styryl boronic acids or esters has been developed.

152 -phenols with secondary and tertiary boronic esters has been explored.

153 cids and racemic beta-stereogenic alpha-keto esters have been developed.

154 g reactions between benzylamines and boronic esters have been investigated.

155 antitative increase in phthalicacid; hex-3yl-ester; hexadecanoicacid methylester etc. whereas, increa

156 es are observed for intramolecular diboronic ester homocouplings when directly compared to the analog

157 s encodes an ortholog of neutral cholesterol ester hydrolase 1 (NCEH-1), an IIS downstream protein th

158 Ester hydrolysis by extracellular carboxylesterases is c

159 l %)-catalyzed cyclopropanation, followed by ester hydrolysis under epimerizing conditions.

160 we found that they are also able to perform ester hydrolysis when attached to a protein.

161 Overall, sorbitan esters impacted cocoa butter crystallization kinetics, t

162 r during the formation of a methanesulfonate ester in the 1-pot activation/displacement/deprotection

163 ss to different 1,4-disubstituted (Z)-enynyl esters in excellent yields.

164 so afforded (Z)-alpha,beta-unsaturated amino esters in moderate to good yields.

165 , phospholipids, cholesteryl esters, and wax esters in OG-treated sebocytes.

166 owing a photobleach and 5-fold lower retinyl esters in the RPE.

167 he presence of visible light to give boronic esters in which two new C-C bonds have been created.

168 and release, and cholesterol and cholesterol esters increased linearly up to 25 mm glucose.

169 In addition, PKC activation by phorbol ester induced agonist-independent KOPR phosphorylation.

170 Sucrose esters induced an unstable system after gastric conditio

171 Starting from the same monoboronic ester intermediates, an intermolecular version of this a

172 enging unsymmetrical N-allyl-N-methylglycine esters is also tolerated under the catalytic relay condi

173 of N-hydroxytetrachlorophthalimide (TCNHPI) esters is crucial to the success of the transformation,

174 opylated and tert-butylated triarylphosphate esters (ITPs and TBPPs), which have similar or greater n

175 e is achieved and functional groups, such as ester, ketone, nitrile, nitro, and triazene are well tol

176 mediate boronate occurs with both halide and ester leaving groups.

177 e and C6-compounds levels, and had increased ester levels in relation to control C.

178 the drug through a hydrolytically degradable ester linkage to a common hydrophilic polymer, polyvinyl

179 plex G4K(+) borate hydrogels by using borate ester linkages (Pt-G4K(+)B hydrogel).

180 nd with the tri(ethyleneoxy) arm para to the ester linkages, "short-armed" cryptand 3, did display a

181 polyether track by the formation/breakage of ester linkages.

182 bes the formation of a prototypical boronate-ester linked 2D COF known as COF-5 from its 2,3,6,7,10,1

183 with enhanced stability compared to boronate ester-linked systems and with broad monomer scope.

184 All four esters (methyl, hexyl, dodecyl and octadecyl dihydrocaff

185 The presence and location of the galloyl ester moiety were essential for inhibitory potency.

186 asked by an aromatic group and an amino acid ester moiety, which are enzymatically cleaved-off inside

187 rocarbons of different natures, fatty acids, esters, monoglycerides, fatty amides, aldehydes, ketones

188 ar substrate with an additional organosulfur ester (MRC) and a substrate containing zerovalent iron a

189 mall interfering RNA-releasing poly(amine-co-ester) nanoparticles, distinguished by their high conten

190 eriae strain (DSM43989) lacking mycolic acid esters neither bound Mincle nor activated macrophages.

191 base), and functional groups such as methyl ester, NH amido, and enolizable keto moieties are found

192 dical precursor includes alpha-iodo ketones, esters, nitriles, primary amides, alpha-fluorinated halo

193 bitors, captopril and fosinopril (a pro-drug ester of fosinoprilat), were tested for larvicidal activ

194 Thus, the glyceryl ester of prostaglandin E2, PGE2-G, mobilizes Ca(2+) and

195 cts) can lead to the formation of fatty acid esters of 2-monochloropropane-1,3-diol, 3-monochloroprop

196 sent study examines the structures of borate esters of BINOL that are produced with different stoichi

197 Serum levels of the novel fatty acid esters of hydroxy fatty acids (FAHFAs) were increased an

198 The recent discovery of fatty acid esters of hydroxy fatty acids (FAHFAs), lipids with pote

199 For the first time, caffeic acid esters of isocitric and several aldaric acids were isola

200 g for the first time those of the protons of esters of phytol and of geranylgeraniol.

201 Five monoacyl and three diacyl esters of trans-cinnamic acids and quinic acid were iden

202 e methylsiloxanes (VMSs) and organophosphate esters (OPEs) are two suites of chemicals that are of en

203 se flame retardants included organophosphate esters (OPEs), brominated flame retardants (BFRs), and D

204 dants: brominated (BFRs) and organophosphate esters (OPEs).

205 A radical stabilizing group such as an ester or ketone moiety at the C3-position of indole lead

206 or quaternary amine and their distance to an ester or related center.

207 raightforwardly cleaved to the corresponding esters or amides using a retro-Friedel-Crafts reaction.

208 redox-active complex with either the boronic esters or the trimeric form of the boronic acids (boroxi

209 tive macrocyclizations of bis(vinyl boronate esters) or ring-closing metathesis reactions followed by

210 nd of biodegradable polymer, poly(beta-amino ester) (PBAE), with PBAE conjugated with 5kDa polyethyle

211 sed on [6,6]-phenyl-C61 -butyric acid methyl ester (PC61 BM).

212 phene) (P3HT)-phenyl-C61-butyric acid methyl ester (PCBM) mixture, and found to predict morphologies

213 The effect of 0.1-0.7% (w/w) of polyglycerol esters (PGEmix-8) on palm oil crystallization was studie

214 etimibe showed a 173% higher LDL-cholesteryl ester plasma disappearance rate (P < 0.001 vs. control)

215 in dipalmitate and further minor xanthophyll esters, prevailing in a presumably liquid-crystalline st

216 Sucrose esters prevented coalescence during 7days since the drop

217 reveal electron density consistent with the ester product being formed in crystallo.

218 The methyl ester products were obtained in >90% yield in nearly all

219 illing on carotenoid accumulation and lutein ester profile including fatty acid selectivity (palmitic

220 ntative maceration and ageing factors on the ester profiles of Pedro Ximenez sparkling wines was eval

221 acetoxybenzyl-based prodrugs with additional ester promoiety(ies) on carboxylate(s) were examined for

222 Application of tert-butyl ester protecting groups for erythro-beta-d-methylasparti

223 The alpha,gamma-dienyl thiol esters provide for a one-pot tandem 1,4-addition-nucleop

224 ve energies of the glycoside-derived boronic esters provides results that are qualitatively consisten

225 Wax ester provisioning decreased after vertically transmitti

226 n properties of hydrophilic tetracarboxylate ester pyrroline nitroxides 1 and 2, which serve as model

227 Allylboronic esters react readily with carbonyls and imines (pi-elect

228 Boronic esters react with 2-lithiated indoles to form boronate i

229 phosphine borane with gamma-iodo-alpha-amino ester reagents under phase-transfer catalysis (PTC).

230 ',N'-tetraacetic acid tetrakis(acetoxymethyl ester) reduced cAMP levels in PC1-knock-out cells.

231 Here, we investigated O-acetyl ester removal and sialic acid degradation by Bacteroidet

232 he current applications of boronic acids and esters require materials with very low levels of transit

233 rols (TAGs), cholesteryl esters, and retinyl esters (REs).

234 metrical diboronic acid that forms a boronic ester reversibly with serine 117.

235 A new series of phenolic glycoside esters, saccharumoside-B and its analogs (9b-9n, 10) hav

236 to sustain the native vitamin B1 phosphorus esters, sample preparation is crucial.

237 emistry because they are orthogonal to other esters, should be considered with care as participating

238 lated mono- and di-substituted double bonds, esters, silyl ethers, and silyl enol ethers).

239 Seven silicon(IV) phthalocyanine carboxylate esters (SiPcs, 1-7) with non-, partially- and per-fluori

240 The bisphosphonate esters stimulated gammadelta T cells to secrete TNF-alph

241 terature on Wolman's disease and cholesteryl ester storage disease, and discuss available treatments,

242 Cholesteryl ester storage disorder arises later in life and is less

243 culum, where it was converted to cholesteryl esters stored in lipid droplets when ORP1L was bound to

244 g fluorescein dilaurate (FDL), a fluorogenic ester substrate, into the polyester matrix and on monito

245 lectivity to the hydrogenation of alpha-keto esters such as ethyl pyruvate.

246 ing different polyethylene glycol fatty acid esters such as Labrasol, Cremophor EL, Gelucire 44/14 an

247 to dosing with TCA cycle metabolite pro-drug esters, suggesting that the high levels of cellular 2OG

248 including esters, aryl halides, aryl boronic esters, sulfonamides, alkyl tosylates, and alkyl bromide

249 and sterols, mainly triglycerides and sterol esters, surrounded by a single monolayer of phospholipid

250 selectively establish the E,Z-diene part, an ester-tethered ring-closing metathesis/base-induced elim

251 iderably lower levels of higher alcohols and esters than S288c and L04.

252 evised a new synthesis of zincophorin methyl ester that proceeds in just nine steps in the longest li

253 The boronic esters that are obtained as direct products of these rea

254 lving cleavage of the C(acyl)-O bond of aryl esters that proceed under mild conditions are reported.

255 interaction between wine proteins and ethyl esters, the effects induced by these fermentative aroma

256 .LiCl) carbenoids in the presence of boronic esters, thus allowing efficient and highly stereospecifi

257 is reported using the cyanopivaloyl (PivCN) ester to ensure effective neighboring group participatio

258 lyzes the isomerization of all-trans-retinyl esters to 11-cis-retinol, is also the isomerase enzyme r

259 lorovinylpyridines with o-aminophenylboronic esters to access pyridobenzazepines is described.

260 ative homocoupling of aryl boronic acids and esters to biphenyls has been recognized as a common bypr

261 The inhibition of cholesteryl ester transfer protein (CETP) by anacetrapib reduces LDL

262 Some cholesteryl ester transfer protein (CETP) inhibitors lower low-densi

263 e TMD-VOO intervention decreased cholesteryl ester transfer protein activity (relative to baseline, P

264 Despite years of development, no cholesterol ester transfer protein inhibitor has yet been approved f

265 LE: Therapies that inhibit CETP (cholesteryl ester transfer protein) have failed to demonstrate a red

266 The development of CETP (cholesteryl ester transfer protein) inhibitors has had a long and di

267 a dilithio phenolate species with a boronic ester, treatment with Ph3 BiF2 or Martin's sulfurane gav

268 Readily accessed allylic hydroxylamine esters undergo copper hydride-catalyzed intramolecular h

269 secondary and tertiary alkyl or aryl boronic esters undergo deborylative three-component coupling to

270 ha-(1'-fluoro)-beta-(phenylsulfonyl)vinyl AA-esters undergo smooth sulfone-stannane interchange to st

271 , the SR-B1-linked selective HDL-cholesteryl ester uptake pathway is now being evaluated as a gateway

272 duction of hydroxycinnamoyl-coenzyme A (CoA) esters using NADPH to produce hydroxycinnamyl aldehyde p

273 mmetric hydrogenation of trisubstituted enol esters using Rh catalysts bearing chiral phosphine-phosp

274 by TMSOTf, no further reaction of the formed ester was detected.

275 cal behavior of a C60-phosphine borane amino ester was investigated by cyclic voltammetry and spectro

276 kynes to racemic beta-stereogenic alpha-keto esters was achieved in high levels of stereoselectivity,

277 xidative properties of the resulted purified esters was investigated using beta-carotene bleaching (B

278 Ketones, aldehydes, and esters were also successfully reduced under mild conditi

279 be present in their free form (no carotenoid esters were detected).

280 hydroxyphthalimide (NHPI) based redox-active esters were found to be convenient starting materials fo

281 Lutein esters were more stable than free carotenoids in vivo an

282 as cryptocapsin, capsoneoxanthin, and their esters were most abundant in orange-fleshed fruit, where

283 These esters were produced by eight phylogenetically related s

284 Terpenes followed by higher alcohols and esters were the predominant classes in the ripening stag

285 molecule, 1-pyrenebutanoic acid succinimidyl ester, which is composed of a pyrene and a reactive succ

286 ACBP binds very-long-chain acyl-CoA esters, which is required for its ability to stimulate C

287 the corresponding terminal alkynes and silyl esters, which is supported by density functional theory

288 highest contents of pyrazines, terpenes and esters, while teff, buckwheat and rice flours presented

289 cted for the synthesis of four other n-alkyl esters with different chain-lengths.

290 to afford ortho-substituted benzylic boronic esters with formal 1,1'-benzylidene insertion into the C

291 nes gave the corresponding secondary boronic esters with high ee.

292 o hydroboration to provide secondary boronic esters with high regio- and enantiocontrol.

293 perature favoured the accumulation of lutein esters with linoleic acid and the synthesis of regioisom

294 The synthesis of glucose esters with palmitic acid, lauric acid and hexanoic acid

295 coupling of representative (Z)-beta-iodoenol esters with terminal alkynes, alkynols, and 1,3-enynes a

296 sition to provide fully substituted glycolic esters with three contiguous stereocenters.

297 ing valuable, enantio-pure skipped 1,4-diene esters (with two configurationally defined double bonds)

298 nd characterize an analogue (pepstatin hexyl ester) with low nanomolar activity.

299 vicinal diols and alpha-hydroxy propargylic esters without loss in enantiopurity.

300 able carboxylic acids into versatile boronic esters would be highly enabling for synthesis.