ライフサイエンスコーパス: carbodiimide

1 ylaminopropyl) carbodiimide, a water-soluble carbodiimide.

2 up in the presence of an activator such as a carbodiimide.

3 ilitated by 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide.

4 tion with a positively charged water-soluble carbodiimide.

5 nt with N-ethyl-1-3-[3-(dimethylamino)propyl]carbodiimide.

6 lamine and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide.

7 -linked by 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide.

8 itated by 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide.

9 linked with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide.

10 eaction with 1-ethyl-3-[(diethylamino)propyl]carbodiimide.

11 ic cross-linker, N- ethyl-3-(3-diaminopropyl)carbodiimide.

12 e plates by 1-ethyl-3(3-dimethylaminopropyl) carbodiimide.

13 reaction cycle driven by the hydration of a carbodiimide.

14 ctive sites engaging sequentially to produce carbodiimide.

15 dianhydride macrocycles on treatment with a carbodiimide.

16 zirine, which photorearranges to give methyl carbodiimide.

17 azone and 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide.

18 inked to apoptotic leukocytes using ethylene carbodiimide.

19 ion to 1 H-diazirines and hence rearrange to carbodiimides.

20 hydrophosphination of alkynes, alkenes, and carbodiimides.

21 sceptibility of the V-PPase to inhibition by carbodiimides.

22 yl- and silylnitrile imines) or rearrange to carbodiimides.

23 s and the C horizontal lineN double bonds of carbodiimides.

24 range to 1H-diazirines, imidoylnitrenes, and carbodiimides.

25 he photoisomerization of nitrile imines into carbodiimides.

26 which upon thermolysis isomerize to bridging carbodiimides.

27 Carbodiimide 10, cyanamide 12, N-cyanomethyleneimine 13,

28 Using carbodiimide, (111)In-DOTA-ChL6 (DOTA is dodecanetetraac

29 via thermolysis of the pyridannulated enyne-carbodiimides 14, 19, and 23 were established.

30 sphorane 14 produced in situ the benzoenynyl carbodiimides 15.

31 On treatment of 1a with a carbodiimide(21,25-27), intramolecular anhydride formati

32 lso produced in situ the benzannulated enyne-carbodiimides 25, which on thermolysis gave the isoquino

33 Thermolysis of the enyne-carbodiimide 42 having a methoxymethyl substituent at th

34 dinitrogen and sulfur to form the respective carbodiimides 5a,b as sole photoproducts.

35 the quantum yields for the formation of the carbodiimides 5a,b were modest and showed little change

36 Thermolysis of the enyne-carbodiimides 7 having the central carbon-carbon double

37 rd 32 by conducting thermolysis of the enyne-carbodiimide 7e in the presence of 5 equiv of dimethylph

38 talyzed by 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide, a water-soluble carbodiimide.

39 f PEDF with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide abolished it, implicating the PEDF aspartic

40 We have utilized labeling with carbodiimide-activated [14C]AGA to identify peptides 120

41 derivatized protein, and (ii) binding of the carbodiimide-activated terminal phosphate group of the C

42 , whereby 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide activates a carboxyl group followed by nucl

43 GNS were coupled with uPAR-Ab via carbodiimide activation chemistry with 1-ethyl-3-(3-dime

44 The carbodiimide activation of carboxylate groups occurs onl

45 d through a streptavidin-biotin bridge via a carbodiimide activation protocol.

46 Reactions with ketenes and carbodiimides afford four-membered anionic heterocycles

47 o syngeneic splenic leukocytes with ethylene carbodiimide (Ag-coupled splenocytes [Ag-SP]) has been d

48 ree polymer chains yields, on treatment with carbodiimide, an IPN with a fracture energy of 2400 J/m(

49 d with 1-ethyl-3-[3-(trimethylammonio)propyl]carbodiimide and [35S]sulfanilic acid.

50 omethane, benzophenone and N,N'-di-isopropyl carbodiimide and by density functional theory.

51 Ugi treated with carbodiimide and glycine ethyl ester produced five discr

52 ed to a dendrimer in a reaction catalyzed by carbodiimide and imidazole.

53 nas and optic nerves were fixed overnight in carbodiimide and labeled with an antiserum to histamine

54 a simple 1-ethyl-3-(3-(dimethylamino)propyl)-carbodiimide and N-hydroxysuccinimide (EDC/NHS) chemistr

55 SA) using N-ethyl-N'-(3-dimethylaminopropyl) carbodiimide and N-hydroxysuccinimide (EDC/NHS) chemistr

56 e by using 1-Ethyl-3-(3-dimethylaminopropyl)-carbodiimide and N-Hydroxysuccinimide coupling reagents,

57 oteins with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide and N-hydroxysuccinimide revealed that carb

58 mutagenesis and chemical cross-linking using carbodiimide and N-hydroxysuccinimide.

59 reagents, 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide and sulfo-N-hydroxysuccinimide.

60 orm an amide derivative with a water-soluble carbodiimide and the electrophoric amine, AMACE1; (3) pu

61 to succinylated hemocyanin by water-soluble carbodiimide and was used as an immunogen to produce pol

62 [4+2] annulation of thioimidates with vinyl carbodiimides and an alkyne hydroamination employing 2-a

63 Divergent reactivity observed with carbodiimides and CO(2) implies an ambiphilicity in the

64 nd Ph(Me)C(H)Bpin, and (ii) hydroboration of carbodiimides and pyridine to form N-boryl formamidines

65 , alkyne, N 2, alkene, diazene, azide, CO 2, carbodiimide, and Bronsted acid containing substrates.

66 substrates such as alkene, pyridine, imine, carbodiimide, and isocyanides.

67 cal mol(-1) for hydrazoic acid, nitrilimine, carbodiimide, and ketenimine, respectively.

68 ction with 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide, and the peptide quenched the fluorescence

69 ndency to chemically and thermally eliminate carbodiimide, and the scarcely observed ring expansion b

70 oup of N-DNW using ethyl(dimethylaminopropyl)carbodiimide as the coupling agent and N-hydroxysuccinim

71 ng ethylenedicysteine with glucosamine, with carbodiimide as the coupling agent.

72 hanism, DFT studies were performed affirming carbodiimide as the crucial intermediate for the interco

73 tal-mediated catalytic addition of amines to carbodiimides as an atom-economical alternative to the c

74 The use of carbodiimides as fuels to generate transient aqueous car

75 ides, are converted to phosphoramidates with carbodiimide assistance.

76 nic acid mono methyl esters with diisopropyl carbodiimide at ambient temperature leads to clean stere

77 alizing the PA sorbent with oligo dT20 using carbodiimide-based amide linker chemistry.

78 intact tissues, we developed a method using carbodiimide-based chemistry to stably retain RNAs in cl

79 The usual strategy has employed carbodiimide-based condensing reagents for activation of

80 e reaction of 3-azidopropanoic acid with the carbodiimide-based coupling reagent DIC leads to a six-m

81 a chemical reaction cycle that hydrolyzes a carbodiimide-based fuel.

82 gainst ALP (anti-ALP) were immobilized using carbodiimide bioconjugation process.

83 d gold electrode surface by the formation of carbodiimide bond.

84 itrile imines isomerize to the corresponding carbodiimides both thermally and photochemically.

85 ss-linker, 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide, can link the N-terminal G-S extension of t

86 e reactions of isocyanates, isothiocyanates, carbodiimides, carbon disulfide, and carbon dioxide with

87 Herein, we show that NHC-carbodiimide (CDI) adducts can be masked precursors for

88 covalently attached onto the electrode using carbodiimide chemistry between the carboxylic groups of

89 oside was functionalized with hexylamine via carbodiimide chemistry compatible with the absence of hy

90 nstrate that capping acidic side chains with carbodiimide chemistry obstructs this pathway, restoring

91 ferent length covalently immobilized through carbodiimide chemistry on the surface of rGO-CMC-modifie

92 The method uses carbodiimide chemistry to footprint carboxylic residues,

93 which can also be functionalized by classic carbodiimide chemistry with N-hydroxysuccinimide (NHS).

94 Using the simple and versatile carbodiimide chemistry, Abs were attached to the carboxy

95 Using carbodiimide chemistry, functionalized probe DNA strands

96 were coupled to phosphorylated primers using carbodiimide chemistry.

97 mitting surface functionalization via simple carbodiimide chemistry.

98 ovalent immobilization of antibodies through carbodiimide chemistry.

99 of proteins to the particles using standard carbodiimide chemistry.

100 and then conjugating the anti-A IgG through carbodiimide chemistry.

101 lucose transporter-1 (GLUT-1) antibodies via carbodiimide chemistry.

102 Here, we show that carbodiimides constitute a simple class of chemical fuel

103 an efficient catalyst for the guanylation of carbodiimides, converting a wide range of aniline substr

104 e quantum dots (QDs) on carboxylated GRs via carbodiimide coupling chemistry, followed by the immunor

105 amenable to covalent modification via simple carbodiimide coupling chemistry, which is achieved by fu

106 by plasma activating the PMMA and the use of carbodiimide coupling chemistry.

107 tibody was immobilized on to its surface via carbodiimide coupling method.

108 band UV exposure of the polymer surface, (2) carbodiimide coupling of amine-terminated oligonucleotid

109 mines to glutamic acid side chains through a carbodiimide coupling reaction.

110 F through a 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide coupling reaction.

111 was covalently conjugated to afGQDs through carbodiimide coupling reaction.

112 covalently tethered onto gold electrodes via carbodiimide coupling to cysteamine-modified gold electr

113 Carbodiimide coupling, cooper-mediated 'click' coupling,

114 NS1 comparing copper free click coupling to carbodiimide coupling, one of the most common approaches

115 opylene carbonate) (PEG-PCC) copolymer using carbodiimide coupling, which self-assembled into micelle

116 Both mAbs were conjugated to SarAr using carbodiimide coupling.

117 otide probes to these surface groups through carbodiimide coupling.

118 om carboxyl-coated polystyrene particles via carbodiimide coupling.

119 ugated to simple amino acids and peptides by carbodiimide coupling.

120 to screen-printed dual carbon electrodes via carbodiimide coupling.

121 ii) stabilization of fragile sialic acids by carbodiimide coupling; (iii) release of N-glycans by PNG

122 oint at the end of a PEG chain combined with carbodiimide-coupling to attach two TA groups per PEG ch

123 GOx) at the DLC surface was realized through carbodiimide covalent linkages.

124 Using the same carbodiimide cross-linker chemistry to conjugate anti-EG

125 ubes covalently attached to chitosan via the carbodiimide crosslinker EDC followed by chitosan electr

126 A carbodiimide crosslinker was used for crosslinking radio

127 immobilizing Con A on a 5MHz gold crystal by carbodiimide crosslinking chemistry.

128 olving an intramolecular ring closure of the carbodiimide-derived phosphazene intermediate is given.

129 Contrary to its oxide analogue, iron carbodiimide does not require heavy treatments (such as

130 compound, 1-ethyl-3-(3'dimethylaminopropyl)-carbodiimide (ECDI), to couple the immunodominant MPO pe

131 venous injection of peptide-pulsed, ethylene carbodiimide (ECDI)-fixed splenic antigen-presenting cel

132 therapy that utilizes infusions of ethylene carbodiimide (ECDI)-treated donor splenic antigen-presen

133 re bound by the cross-linking agent ethylene carbodiimide (ECDI).

134 donor splenocytes cross-linked with ethylene carbodiimide (ECDI-SPs) has been demonstrated to effecti

135 ated with 1-ethyl-3-(3'-dimethylaminopropyl)-carbodiimide (ECDI-SPs) provide permanent donor-specific

136 Analogs of syndecan-1 were produced by carbodiimide (EDAC) conjugation of glycosaminoglycan (GA

137 Ib-2) using 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDAC), which modifies acidic amino acid re

138 give poly(anhydrides) when treated with the carbodiimide EDC.

139 density of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) activated anti-LCN2 capture antibodie

140 inking with 1-ethyl-3-(dimethylamino-propyl)-carbodiimide (EDC) allowed the isolation of a BPL:apo-BC

141 , involving 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) and 1-cyano-4-dimethylaminopyridinium

142 ss-linker 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide (EDC) and analyzed by gel electrophoresis.

143 resence of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) and imidazole.

144 1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) and N-Hydroxysuccinimide (NHS) chemis

145 activator 1-ethyl-3-(3-dimethylamino)propyl)carbodiimide (EDC) and the catalyst 1-hydroxybenzotriazo

146 ation with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) for visualization of EVs in a range o

147 gomers with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) in the presence of linear plasmid DNA

148 roups with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) or 2-chloro-1-methylpyridinium iodide

149 to BSA by 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) to form GAMP(CNBr)AH-BSA and GAMP(CDA

150 1-Ethyl 3-[3-(dimethylamino)propyl]carbodiimide (EDC) was found to promote formation of sto

151 ter-soluble 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) was used to cross-link proteins with

152 s-linker, 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide (EDC), and the Paracoccus membranes were us

153 g UV-ozone, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), and treated with N-hydroxysuccinimid

154 -linker, l-ethyl-3-[3-(dimethylamino) propyl]carbodiimide (EDC), cross-linked the ND8-G-actin complex

155 ed reagent, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), in a concentration-dependent and sub

156 ss-linker 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide (EDC), referred to as EDC-actin.

157 Carbodiimide (EDC)-based dentin primers preserve hybrid

158 h a novel, 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC)-mediated, chemical cross-linking step

159 e through N-ethyl-N'-(3-dimethylaminopropyl) carbodiimide (EDC)-N-hydroxy succinimide (NHS) chemistry

160 ss-linker 1-ethyl-3-[3-dimethyl-aminopropyl]-carbodiimide (EDC).

161 with ADH and 1-ethyl-3(3-dimethylaminopropyl carbodiimide (EDC).

162 ing agent 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide (EDC).

163 ocol with 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide (EDC).

164 mistry with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC)/N-hydroxysuccinimide (NHS) as a heter

165 We discovered that using the soluble carbodiimide, EDC, to cross-link RNA to nylon membranes

166 opyl ester of methionine (MIPE), mediated by carbodiimide EDCI, 1, and HOBt, 2, have been studied in

167 ization of the tertiary allylic amine to the carbodiimide equilibrates with a zwitterionic intermedia

168 In particular, iron carbodiimide, FeNCN, can be efficiently used as negative

169 nostaining for the cysteinyl leukotrienes in carbodiimide-fixed cells, we show, for the first time, t

170 ated epitopes, by i.v. injection of ethylene carbodiimide-fixed peptide-pulsed APCs, either before di

171 reatment with Ag (peptide)-coupled, ethylene carbodiimide-fixed syngeneic splenocytes (Ag-SP) is a po

172 istration of myelin peptide-pulsed, ethylene carbodiimide-fixed syngeneic splenocytes, but not solubl

173 dition of the vinyl pyrrolidine amine to the carbodiimide followed by a 1,3-diaza-Claisen rearrangeme

174 reaction proceeds through the formation of a carbodiimide, followed by a sequential addition--dehydra

175 pling to a keto function and a water-soluble carbodiimide for coupling to a carboxyl function.

176 (LNA) and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide for cross-linking the RNA to the membrane.

177 tric studies into tosyl azide activation and carbodiimide formation enabled the isolation and crystal

178 ites, and its ensuing catalytic activity for carbodiimide formation.

179 es, efficiently catalyzes the hydration of a carbodiimide fuel to the corresponding urea waste, with

180 Carbodiimide-fueled anhydride bond formation has been us

181 e in the storage modulus is possible through carbodiimide fueling.

182 is work, we show that N-heterocyclic carbene-carbodiimide-functionalized Cu catalysts display a remar

183 rea intermediates that, in the presence of a carbodiimide-functionalized resin, cyclize to benzazoles

184 precursors that give IPNs on treatment with carbodiimide give much higher fracture energies (i.e., r

185 dipolar cycloaddition of azine N-oxide with carbodiimide has been demonstrated.

186 The use of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide HCl (EDC) has recently been investigated fo

187 Accordingly, catalysis of carbodiimide hydration by the motor molecule continuousl

188 resence of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDAC) and then hybridized wi

189 tivated by 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC) and N-hydroxysuccinimid

190 tion using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC) and physical adsorption

191 MBs using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC) chemistry.

192 YiiP with 1-ethyl-3-[3-dimethylaminopropyl] carbodiimide hydrochloride (EDC) resulted in a dimeric c

193 fied with 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride (EDC), is not associated with

194 ied using 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride (EDC), Mn2+ is photooxidized

195 g reagent, 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (EDC), to localize regions of

196 ng reagent, 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride (EDC), was used to covalently

197 e optimized 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride (EDC)-catalyzed amide bond fo

198 loped a new 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDCI)-mediated oxazole rearr

199 sue with 1-ethyl-3-[3-(dimethylamino)propyl]-carbodiimide hydrochloride and (ii) removing highly abun

200 MTP) using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and N-hydroxysulfosuccinimide

201 s-linked by 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride to probe for the aggregation

202 nol using 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride.

203 nopril by 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride/N-hydroxysuccinimide coupling

204 veloped to access a variety of mono- and bis-carbodiimides in good yield and high purity on multigram

205 Using the method of water-soluble carbodiimide-induced chemical ligation, four 27-member o

206 proximity was assessed by the efficiency of carbodiimide-induced cross-linking and the orientation b

207 imple chemically fueled system that exhibits carbodiimide-induced geometry changes.

208 activated thiourea through the formation of carbodiimide intermediate.

209 The five-membered ring carbodiimide is a stable structure, possibly isolable.

210 ture of this reaction is that no part of the carbodiimide is incorporated into the transient species;

211 d actinide-catalyzed addition of alcohols to carbodiimides is presented.

212 enimines 5 with various heterocumulenes like carbodiimides, isocycanates, isothiocyanates and ketenim

213 Monosubstituted carbodiimides isomerize thermally to the corresponding c

214 cted to locate the transition states between carbodiimides isomers.

215 for the detection of HT-2 mycotoxin based on carbodiimide linking of the microelectrode surface and H

216 ron compound, several other transition-metal carbodiimides M(x)(NCN)y with M=Mn, Cr, Zn can cycle suc

217 s on the CNTs' tips that were modified using carbodiimide mediated coupling between the carboxylic ac

218 Carbodiimide mediated couplings with amines were then us

219 conjugated to bovine serum albumin (BSA) by carbodiimide-mediated chemistry, a key step in the reali

220 After carbodiimide-mediated cross-linking, Lys-3 of thymosin b

221 -coupling reactions for building blocks, and carbodiimide-mediated esterification for building up the

222 onjugates of Vi and OAcP were synthesized by carbodiimide-mediated synthesis with adipic acid dihydra

223 oxal, and 1-cyclohexyl-3-(2-morpholinoethyl)-carbodiimide metho-p-toluene sulfonate (CMCT) offers the

224 nd including 1-cyclohexyl(2-morpholinoethyl) carbodiimide metho-p-toluene sulfonate (CMCT) reactiviti

225 s include 1-cyclohexyl-3-(2-morpholinoethyl) carbodiimide metho-p-toluene sulfonate (CMCT; to probe U

226 l sulfate, 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluene sulfonate, and kethoxal; co

227 cans with 1-cyclohexyl-3-(2-morpholinoethyl) carbodiimide metho-p-toluene sulfonate, dimethyl sulfate

228 ate (DMS), 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate (CMCT), and beta-e

229 ulfate and 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate probing, mutate-an

230 hoxal, and 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate, can be combined i

231 repared by employing an N-hydroxysuccinimide/carbodiimide method.

232 The sensitivity of enzyme to water-soluble carbodiimide modification of carboxyl groups prompted ev

233 Carbodiimide modification of EmrE has been studied using

234 fferent substrate analogs to protect against carbodiimide modification of Glu269, it is suggested tha

235 Covalent inhibitors bearing a carbodiimide moiety are shown to covalently label KRAS(G

236 in the presence of ethyl(dimethylaminopropyl)carbodiimide / N-hydroxysuccinimide (EDC/NHS) between th

237 ix-sense-selective polymerization of achiral carbodiimide, N-(1-anthryl)-N'-octadecylcarbodiimide (1)

238 s-linked with 1-ethyl-3-(dimethylaminopropyl)carbodiimide/N-hydroxylsulfosuccinimide in a 1:1 complex

239 accomplished using 3-(3-dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide (EDC/NHS) coupling to

240 ing by 1-ethyl-3-(3-dimethylaminopropyl) and carbodiimide/N-hydroxysuccinimide (EDC/NHS) was adopted

241 e N-cyclohexyl-N'-(4-(dimethylamino)naphthyl)carbodiimide (NCD-4) fluorophore, whereas tryptophan is

242 razoic acid (NH=N=N), nitrilimine (NH=N=CH), carbodiimide (NH=C=NH), or ketenimine (NH=C=CH2) plus on

243 N-Heterocyclic carbene-carbodiimide (NHC-CDI) adducts are versatile compounds t

244 ctron oxidation of an N-heterocyclic carbene-carbodiimide (NHC-CDI) zwitterionic adduct.

245 uccinimide/1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide) (NHS/EDC)-activated self-assembled monolay

246 by EDC (1-ethyl-3-(3-(dimethylamino)propyl)-carbodiimide)/NHS ( N-hydroxysulfosuccinimide) activatio

247 of imidoylnitrenes, which also rearrange to carbodiimides or add intramolecularly to aryl substituen

248 roportionated Ti(IV) complex having transoid carbodiimides, [(PN)(2)Ti(NCNAd)(2)] (9).

249 Using carbodiimide polyesterification, these stress-responsive

250 provides a pathway involving O2 to give the carbodiimide product whereas homogeneous metal ion catal

251 Carbodiimide-promoted cyclization of zwitterionic aminop

252 was 75-fold higher compared with traditional carbodiimide protein coupling.

253 with primary amines (H2N-R') and O2 to give carbodiimides (R-N=C=N-R') at room temperature and above

254 e step of the process is the formation of RE carbodiimides (RE(2)(CN(2))(3)) along with Pt particles.

255 CHO-H4PteGlun were cross-linked to SHMT by a carbodiimide reaction to Lys-450 which resides in a stre

256 the desired antibody was carried out by the carbodiimide reaction.

257 a significant proportion of the decrease in carbodiimide reactivity occurs specifically in a nanopep

258 In contrast, carbodiimide reactivity of mutant Glu269-->Asp that exhi

259 that substrate protects the permease against carbodiimide reactivity.

260 ciency, MMOH and MMOR were cross-linked by a carbodiimide reagent and analyzed by specific proteolysi

261 The reaction is mediated with water-soluble carbodiimide reagent and is assumed to result in a prima

262 ocyanate and imidoyl isothiocyanate-thioacyl carbodiimide rearrangements.

263 Computational studies of alicyclic carbodiimides (RN horizontal lineC horizontal lineNR) (r

264 ing differential labeling by a water-soluble carbodiimide, seven specific carboxylates in RIalpha wer

265 e first time, that treatment of capsule with carbodiimide significantly reduced recognition by capsul

266 tamethylcyclopentadienyl, 1b) with different carbodiimide substrates RN horizontal lineC horizontal l

267 somerization, or C-C coupling of the applied carbodiimide substrates, respectively, to form unusual m

268 ion of the corresponding benzannulated enyne-carbodiimides, such as 10, followed by a formal intramol

269 ation with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide that irreversibly immobilizes the microRNA

270 to tertiary allylic amines are converted to carbodiimides through a reaction with AgOTf/Et(3)N.

271 ving intramolecular addition of the amine to carbodiimide to afford a zwitterionic intermediate follo

272 water acts as a nucleophile and reacts with carbodiimide to deliver the product.

273 d utilizes 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide to derivatize pseudouridine residues.

274 linked using 1-ethyl-3(dimethylamino-propyl) carbodiimide to generate a catalytically active heterodi

275 yde and N-ethyl-1-3-[3-(dimethylamino)propyl]carbodiimide to investigate the organization of the poly

276 ked with 1-ethyl-3-[3(dimethylamino) propyl] carbodiimide to prevent shortening.

277 s were treated with N,N'-dicyclohexyl-[(14)C]carbodiimide to radiolabel the D61 residue on less than

278 diphenylketene and bis(2,6-diisopropylphenyl)carbodiimide to yield the anionic four-membered heterocy

279 ates, isothiocyanates, and in situ-generated carbodiimides to form zwitterionic intermediates that un

280 , produced by the formal [2 + 2] addition of carbodiimides to the P=N bond, have been isolated and ch

281 with EDC (1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide) to prevent shortening, with FHS.

282 vation chemistries, and we demonstrated that carbodiimide treatment under aqueous conditions results

283 ovalent modification of carboxyl groups with carbodiimides using electrospray ionization mass spectro

284 electrochemical activity of transition-metal carbodiimides versus lithium and sodium.

285 go efficient, unimolecular rearrangements to carbodiimides via 1 H-diazirines and imidoylnitrenes und

286 aryl) catalytically metathesize C=N bonds of carbodiimides via an addition/elimination mechanism that

287 Carbodiimide warheads show selectivity toward KRAS(G12D)

288 ted when 1-ethyl-3-[3-(dimethylamino)-propyl]carbodiimide was used as cross-linking agent, whereas th

289 This reagent, N-(2,2-diethoxyethyl)carbodiimide, was convenient to prepare and was stable u

290 cross-linker ethyl-3-(3-dimethylaminopropyl)carbodiimide, we obtained cross-linked heterodimers of b

291 rtant classes of solids such as cyanides and carbodiimides, well known at ambient conditions and comp

292 ng reagent, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide were identified after trypsin digestion of

293 upled with cardiac myosin by use of ethylene carbodiimide, were administered intravenously before dis

294 rosslinking agent before the addition of the carbodiimide, which allowed for the shell crosslinking t

295 th the chemical cross-linking agent ethylene-carbodiimide, which effectively modulate Th1/Th17 diseas

296 oss-linked by 1-ethyl-3-(dimethylaminopropyl)carbodiimide, while subunits a and E could be cross-link

297 astereoselective [4 + 2]-annulation of vinyl carbodiimides with chiral N-alkyl imines has been develo

298 on of anionic secondary phosphine boranes to carbodiimides yields both chiral and achiral phosphaguan

299 Heating the carbodiimide/zwitterion affords a rearrangement product.

300 Heating carbodiimide/zwitterion with a deuterated allyl group re