ライフサイエンスコーパス: diamine

1 N'-dimethyl-N,N'-dipyridine-2-ylpyridine-2,6-diamine).

2 g (R,R)-N,N'-dibenzyl-1,2-diphenylethane-1,2-diamine.

3 O2CPh)2 by N,N,N',N'-tetramethylethylene-1,2-diamine.

4 minobutyl)-N(4)-butyl-6-methylpyrimidine-2,4-diamine.

5 elf-sorting in the presence of the NDI-based diamine.

6 -amino amide or reduced to the corresponding diamine.

7 diamine and an electron-deficient NDI-based diamine.

8 ron(II) chloride, and either monoamines or a diamine.

9 extrusion provided synthetically useful 1,2-diamines.

10 ld be reduced to give spirocyclic amines and diamines.

11 ucts, 1,3-diols, 1,3-amino alcohols, and 1,3-diamines.

12 clic tetraimines based on bis-alkynylbenzene diamines.

13 rivatives and a twisted conformation for the diamines.

14 ine affords differentially protected vicinal diamines.

15 gates and complexes with several widely used diamines.

16 tereoselective fluorescent sensor for chiral diamines.

17 of sparse olfactory sensory neurons by these diamines.

18 tracts, a physiologically relevant source of diamines.

19 sively as bis-solvated dimers with chelating diamines.

20 ess to a wide range of 1,2-disubstituted 1,2-diamines.

21 zene; tmen = N,N,N',N'-tetramethylethane-1,2-diamine].

22 -1) [tmeda = N,N,N',N'-tetramethylethane-1,2-diamine].

23 zeotype has been prepared using the aromatic diamine 1,10-phenanthroline and some of its methylated a

24 Diamines 1 exhibit moderate fluorescence (PhiF = 0.25, 0

25 Diamines 1 were obtained by metal-mediated amine condens

26 l)-N(6)-(2,2,2-trifluoroethyl)-9H-purine-2,6-diamine (1, NEU-1106).

27 Diamine (-)-1 has been prepared in multigram quantities

28 nthesis and resolution of the C(2)-symmetric diamine 2,7-diazabicyclo[4.4.1]undecane [(-)-1] are repo

29 biphenyl-3,3'-dicarboxylate) with the cyclic diamine 2-(aminomethyl)piperidine (2-ampd) produces an a

30 -2-(2-furanyl) thiazolo[5,4-d]pyrimidine-5,7-diamines (2-18) and their pharmacological characterizati

31 A mixture of two triamines, one diamine, 2-formylpyridine and a Zn(II) salt was found to

32 , 8,9-disubstituted-3,9-dihydro-2H-purin-2,6-diamines 21-24 and 6-imino-1-phenyl-8,9-disubstituted-6,

33 N(9)-tetraethylquinolino[7,8-h]quinoline-4,9-diamine (26) is more superbasic than quinolino[7,8-h]qui

34 ]bis{N(4)-[4-(methylamino)butyl])bu tane-1,4-diamine}, 3b, was found to have an optimal balance betwe

35 method for the measurement of five aromatic diamines, 4,4'-methylenedianiline (MDA), 2,4-toluenediam

36 merization of N,N,N',N'-tetraethylbutane-2,3-diamine (4a).

37 rivatives of (-)-1, i.e., the bis-methylated diamine (+)-5 and two diastereomeric tricyclic analogs,

38 chain to the N,N-dimethyl-1,3,5-triazine-2,4-diamine-6-ethyl moiety by NMR spectroscopy, MALDI-TOF ma

39 ne)-b-poly(2-N,N-dimethyl-1,3,5-triazine-2,4-diamine-6-ethyl-2-oxazoline) (PMeOx-PcBOx), and demonstr

40 )tris(N(4)-(4-(methylamino)b utyl)butane-1,4-diamine, 6b, which contained three N-methylhomospermidin

41 loro-n-ethyl-n'-(1-methylethyl)-triazine-2,4-diamine), a prevalent herbicide in the United States, is

42 the synthesis of diverse heteroaromatic 1,2-diamines, a valuable synthetic building block to develop

43 ed circular helicates that are formed from a diamine--a molecular Solomon link and a pentafoil knot--

44 id serving as the carbon source and ethylene diamine acting as the nitrogen source.

45 d enantiomeric composition of chiral amines, diamines, amino alcohols, amino acids, and alpha-hydroxy

46 useful for the synthesis of enantiopure 1,2-diamine and alpha-amino acid derivatives.

47 conditions to yield aminoether, imidazoline, diamine and amino bromine.

48 cture incorporating both a pyrene-containing diamine and an electron-deficient NDI-based diamine.

49 as synthesized by the condensation of linear diamine and dialdehyde subcomponents around copper(I) te

50 thesis and comprehensive characterization of diamine and diimine derivatives of the fluorescent compo

51 lideneaminato)-N'-(2-hydroxyethyl)ethane-1,2-diamine and L(2) is 3,5-di-tert-butylcatechol), which en

52 ide and trans- N, N'-dimethylcyclohexane-1,2-diamine and promotes arylation at the N(1) nitrogen atom

53 ed by electrochemical patterning of ethylene diamine and terminal amine polyethylene glycol chain to

54 where the thiadiazole unit can be reduced to diamine and the obtained diamines can be further condens

55 alyst-free nucleophilic addition between PEG-diamine and vitamin E-functionalized cyclic carbonate.

56 m very simple starting materials such as 1,2-diamines and alkyl 3-oxohex-5-enoates and can be perform

57 For diamines and amino acids, total N-nitrosamine accumulati

58 ming the reactions in the presence of chiral diamines and amino alcohols led to the enantioselective

59 domino reaction, starting from nonprotected diamines and arylglyoxals.

60 -Henry approach to nonsymmetric cis-stilbene diamines and cis-imidazolines.

61 st loadings of commercially available chiral diamines and copper triflate proposed to self-assemble i

62 PAs) have been synthesized using alpha,omega-diamines and omega-aminoalcohols as N-C(x)-N and N-C(y)

63 e coupling of o-phenylenediamine/substituted diamines and substituted aromatic/heterocyclic/aliphatic

64 via asymmetric deprotonation (s-BuLi/chiral diamine) and trapping with Andersen's sulfinate (menthol

65 (-) (mes=mesityl) rather than adducts of the diamine, and it is this ate complex that accounts for th

66 ogenation of a polyurethane to produce diol, diamine, and methanol.

67 of these, alcohols, including 1,2-diols, 1,2-diamines, and amino acids are the most intriguing, and w

68 es (alkanolamines, straight-chain and cyclic diamines, and amino acids), the order of the amine was t

69 avior of zebrafish to cadaverine and related diamines, and concomitant activation of sparse olfactory

70 Here we show that diamine-appended metal-organic frameworks can behave as

71 g inspiration from the crystal structures of diamine-appended metal-organic frameworks exhibiting two

72 we present a detailed investigation of nine diamine-appended variants of the metal-organic framework

73 Vicinal diamines are a common structural motif in bioactive natu

74 Urinary diamines are biomarkers of diisocyanate exposure.

75 ates of aldol reactions catalyzed by vicinal diamines are characterized with density functional calcu

76 , these results demonstrate that short-chain diamines are common substrates for the PACE family of tr

77 Enantioenriched 1,2-diamines are formed in good yields and with excellent en

78 Various mono- and diamines are oxidized into corresponding mononitro deriv

79 Chiral diamines are particularly useful as ligands for asymmetr

80 Vicinal diamines are ubiquitous materials in organic and medicin

81 of N(4)-butyl-5-iodo-6-methylpyrimidine-2,4-diamine as a pure TLR8 agonist, and a detailed structure

82 ic nitroepoxides are transformed into chiral diamines as a single enantiomers (>95:5 er) through a dy

83 g ionic liquid as coagulation and functional diamines as cross-linkers to connect graphene oxide laye

84 mediates for the synthesis of chiral vicinal diamines as has been verified for a representative examp

85 des a convenient approach to vicinal primary diamines as well as other synthetically valuable nitroge

86 l polymerization (SI-ATRP) and hexamethylene diamine (as a spacer arm).

87 ucture consisting of N,N'-di-N-acetyllactose diamine at multiple N-linked sites, one of which at Asn-

88 alen ligand, and not the shape of the chiral diamine backbone of the ligand.

89 eight new Ti(salen) catalysts with modified diamine backbones.

90 d in vitro activity of a cyclohexane-1 R,2 R-diamine-based Pt(IV) derivative containing the histone d

91 yl groups at the 3,5 positions) of pyrazolyl-diamine bifunctional chelators (Pz(2)-Pz(4)) on the phar

92 ported and supported 1,1'-binaphthalene-2,2'-diamine (BINAM) derived prolinamides are efficient organ

93 nzylideneacetone) and chiral 2,2'-binaphthyl diamine (BINAM)-derived phosphoric acids (BDPA, 2,2'-bin

94 ogenation catalyst for the transformation of diamine boranes into cyclic 1,3,2-diazaborolidines, whic

95 ssembly of 2-formylpyridine and C2-symmetric diamine building blocks having differing geometries, inc

96 nyl amine-based trialdehydes and cyclohexane diamine building blocks utilizing the dynamic imine chem

97 wavelengths (lambdamax 495-510 nm) than the diamines but are still slightly blue-shifted from thioin

98 ghly diastereoselective synthesis of vicinal diamines by the treatment of nitroepoxides with primary

99 s induced in A. baumannii by the short-chain diamines cadaverine and putrescine.

100 Readily available phenylene-1,3-diamines can be converted into unprecedented analogues o

101 t can be reduced to diamine and the obtained diamines can be further condensed with the diketones wit

102 ound that the aliphatic primary 1,2- and 1,5-diamines can greatly enhance the fluorescence of this co

103 With the aid of a nickel/diamine catalyst (both components are commercially avail

104 onditions using tethered Ru(II)/eta(6)-arene/diamine catalysts is described, as is the ATH of electro

105 Four vicinal diamine-catalyzed aldol reactions were examined.

106 d the chirality by a stereoselective iridium-diamine-catalyzed asymmetric transfer hydrogenation reac

107 s revealed the enolates to be octahedral bis-diamine-chelated monomers.

108 lkylation with allyl bromide implicate a bis-diamine-chelated-monomer-based transition structure.

109 pyl)-N(3)-(cyclopentadecylmethyl)propane-1,3-diamine compared with dihydromotuporamine C.

110 u(I) ions, which are present as mobile Cu(I) diamine complexes [Cu(I)(NH(3))(2)](+).

111 isolated air- and moisture-stable Ru(II)-NHC-diamine complexes act as versatile precatalysts for the

112 A modular synthesis of Ru(II)-NHC-diamine complexes from readily available chiral N-hetero

113 The well-defined Ru(II)-NHC-diamine complexes show unique structure and coordination

114 e species formed by oxidation of these Cu(I) diamine complexes with oxygen at 200 degrees C, we have

115 enum oxide and molybdate species, nickel(II) diamine complexes, alkali-exchanged stannosilicate molec

116 A series of bimetallic [(NHC)PtX2]2(diamine) complexes have been prepared as a new chemotype

117 Through variation of the diamine component, the reaction can be extended to the s

118 the N(2),N(4)-disubstituted quinazoline-2,4-diamine compound series a suitable platform for future d

119 ce with EDAC/NHS followed by reaction with a diamine compound.

120 The diamine compounds 1 absorb in the UV (lambdamax 324-328

121 Three pyrazolyl-diamine-containing chelators were conjugated to betaAlaN

122 vered that N(2),N(4)-dibenzylquinazoline-2,4-diamine (DBeQ), the least potent among the tested p97 in

123 sNBr2 in the presence of K2CO3, N,N'-ditosyl diamine derivative was obtained in moderate yield.

124 eparation of a diverse range of 1,2- and 1,3-diamine derivatives by selective ring-opening reactions.

125 edure for the synthesis of N-acetyl,N'-tosyl diamine derivatives directly from olefin.

126 opyl-4,5,6,7-tetrahydroben zo[d]thiazole-2,6-diamine derivatives led to development of a lead compoun

127 the synthesis of versatile unsymmetrical 1,2-diamine derivatives.

128 ides have been easily prepared starting from diamines derived from natural amino acids and commercial

129 he diversification of access to cis-stilbene diamine-derived imidazolines provided by this platform s

130 ived phosphoric acids (BDPA, 2,2'-binaphthyl diamine-derived phosphoric acids) is presented.

131 (N(1),N(4)-Di(buta-2,3-dien-1-yl)butane-1,4-diamine dihydrochloride), an inhibitor of SMOX, reduced

132 om 2-aminobenzyl alcohol/1-phenylethanol and diamine/diol, respectively, in a shorter span of reactio

133 mmercially available, classic Noyori Ru(II) -diamine-diphosphine catalysts, well-known in asymmetric

134 s using chelation-assisted removable vicinal diamine directing groups was developed.

135 oduct removal using only one equivalent of a diamine donor (ortho-xylylenediamine) is reported.

136 By employing chiral diphenylethylene diamine (dpen) as ligands bearing electron-withdrawing a

137 entification of long chain aliphatic primary diamine Duomeen O (n-oleyl-1,3-diaminopropane), corrosio

138 mination provided orthogonally protected 1,4-diamine, epsilon-amino carboxylic, and epsilon-amino ket

139 dentine caries arrest capabilities of silver diamine fluoride (SDF) and sodium fluoride (NaF).

140 Silver diamine fluoride (SDF) is found to promote remineralizat

141 Silver diamine fluoride (SDF) is used topically to prevent or a

142 lesions (low certainty) and that 38% silver diamine fluoride solution applied biannually was the mos

143 ivity relationship studies in pyrimidine 2,4-diamines, focusing on substituents at C5.

144 reparation of widely useful, enantioenriched diamines for applications in medicinal chemistry and cat

145 lpha,beta-unsaturated esters gave a range of diamines for elaboration to T1-T8 via a sequence involvi

146 A chiral vicinal diamine forms an enamine-iminium adduct with alpha-ketoe

147 ategy streamlines the preparation of vicinal diamines from multistep sequences to a single chemical t

148 A new diamine-functionalized metal-organic framework comprised

149 romethane-mediated reaction of primary amine/diamine, furfural, and 1,3-diketone.

150 peptide and/or a glucose or biotin ethylene diamine group were synthesized, and the binding capabili

151 B7) hosts around a simple hydroquinol-based, diamine guest (GH2 (2+) ) was investigated by (1) H NMR

152 The synthesis of 1,2-diamines has been achieved through a single-step, tandem

153 or asymmetric synthesis of both syn/anti-1,3-diamines has been developed.

154 s of N(2),N(4)-disubstituted quinazoline-2,4-diamines has been synthesized and tested against Leishma

155 s of N(2),N(4)-disubstituted quinazoline-2,4-diamines has been synthesized and tested against multidr

156 Vicinal aziridine-containing diamines have been obtained with high syn-stereoselectiv

157 Behavioral responses to diamines have not been investigated in zebrafish, a powe

158 Unstable explosive hexamethylene triperoxide diamine (HMTD) is dangerous in quantity and benefits fro

159 riperoxide (TATP), hexamethylene triperoxide diamine (HMTD), and cyclohexanone, with detection limits

160 ction of TATP from hexamethylene triperoxide diamine (HMTD, another common peroxide-based explosive)

161 apeutic payload proflavine (PF, acridine-3,6-diamine hydrochloride), is reported.

162 ion of arylboronic acids with aromatic diol, diamine, hydroxythiol, and dithiol compounds in chlorofo

163 The chiral diamine imparts stereocontrol in the enamine-iminium com

164 repared by the condensation of aryl acid and diamine in polyphosphoric acid medium.

165 -diazides can be smoothly reduced to vicinal diamines in a single step, with high chemoselectivity.

166 alkaloid-derived amines, and chiral vicinal diamines in general, have been determined by density fun

167 ds afforded differentially protected vicinal diamines in good yields with high enantioselectivities.

168 ubstituted lactams to deliver differentiated diamines in moderate to high yields.

169 The reaction affords 1,2-diamines in very good yields and is functional-group-tol

170 The transformation involves a gem-diamine intermediate that undergoes the indolizidine -->

171 Electrochemistry of the diamine is carried out to explore redox properties and s

172 dehydrogenative coupling of methanol and 1,2-diamine is demonstrated.

173 -pyridylation of trans-(R,R)-cyclohexane-1,2-diamine is described here.

174 ine is in the zwitterionic form (pH 9-11) or diamine is in the monocationic form (pH 7-9).

175 inoxalines from both 2-nitroanilines and 1,2-diamines is demonstrated.

176 al N-heterocyclic carbenes (NHCs) and chiral diamines is disclosed for the first time.

177 [(2-methoxyphenyl)-methyl]hexyl]-1,8-octane] diamine) is an M(2)-selective competitive antagonist of

178 -13 dendrimer comprising triazines linked by diamines, is stable across ranges of concentration, pH,

179 with benzene-1,2-diamine or naphthalene-1,8-diamine it affords heterocyclic-fused porphyrins.

180 1000 used previously in some researches and diamine Jeffamine ED-2003 applied for the first time for

181 The disaccharide N,N'-di-N-acetyllactose diamine (LacdiNAc, GalNAcbeta1-4GlcNAcbeta) is found in

182 ir-stable Ni(II) source in the presence of a diamine ligand and a metal reductant to allow late-stage

183 N-(p-tolylsulfonyl)-1,2-diphenylethylene-1,2-diamine ligand have been prepared, characterized, and ev

184 in the presence of a Ni catalyst and chiral diamine ligand.

185 ed with Ni salts in the presence of a chiral diamine ligand.

186 ch shows that the nickel and the coordinated diamine ligands participate in a synergistic way during

187 Novel diamine ligands with spiro indane-2,2'-pyrrolidine scaff

188 The hosts, octa-acid (OA) and hexalene diamine-linked octa-acid (HOA), were shown to complex a

189 Depending on the species, these diamines may also serve as feeding attractants, oviposit

190 d a hydrophobic environment for a molybdenum diamine (Mo-diamine) precursor solution, enabling direct

191 s-link the aldehyde groups of ZIF-90 using a diamine molecule with a conversion efficiency of 70%.

192 raction of both of the two amine groups of a diamine molecule with the sensor is essential for the ob

193 or example, when poly(ethylene glycol) (PEG) diamine monomers were used to form HDCNs, elastic organo

194 By simply using different diamine monomers, the HDCN- and PHT-forming reactions af

195 p demonstrate the versatility of this masked diamine motif in chemoselective, orthogonal transformati

196 Here, using the symmetric diamine N,N'-dimethylpiperazine as a model, we have expe

197 pyridine, N,N,N',N'-tetramethylethylene-1,2-diamine, n-octylamine).

198 (DFOB) and N, N'-di(2-hydroxybenzyl)ethylene-diamine- N, N'-diacetic acid (HBED)) and four Fe(III) (h

199 d nanoparticles (AuNPs) and naphthylethylene diamine (NED) as coupling agent for azo-dye formation, a

200 (1-naphthyl)N,N'-diphenyl-1,1'-biphenyl-4,4'-diamine (NPB) and lowest unoccupied molecular orbital (L

201 modified by electropolymerizing o-phenylene diamine onto the Pt wire microtransducer, followed by th

202 ne)bisphthalimides, whereas with benzene-1,2-diamine or naphthalene-1,8-diamine it affords heterocycl

203 [Pt(Am)(R(COO)2)2], where Am is a chelating diamine or two monodentate am(m)ine ligands and R(COO)2

204 ction of the title compound with benzene-1,4-diamine or with benzene-1,3-diamine yields the correspon

205 one further comonomer comprising monoamines, diamines, or amine-free structures, whose influence on t

206 N, N'-bis(pyridin-2-ylmethyl)cyclohexane-1,2-diamine, OTf = trifluoromethanesulfonate anion) and beta

207 Histaminolytic activity mediated by diamine oxidase (DAO) is present in plasma after inducti

208 Intracellular fluorochrome-labeled diamine oxidase (DAO) was used as a novel functional rea

209 stamine-rich food due to reduced activity of diamine oxidase (DAO).

210 A bienzymatic biosensor employing diamine oxidase (DOx) and horseradish peroxidase (HRP) f

211 Human diamine oxidase (hDAO), required for histamine catabolis

212 6, P = 0.04205), and intracellularly labeled diamine oxidase (P = 0.0003, P = 0.0148).

213 nfection increased diarrhea incidence, blood diamine oxidase activity, and iFABP level, while reducin

214 odular, injectable sensing platform based on diamine oxidase and a phosphorescent oxygen nanosensor.

215 minobutyraldehyde with putrescine oxidase or diamine oxidase as catalysts.

216 The biosensor with diamine oxidase had the lowest measured concentration of

217 However, individuals who take monoamine and diamine oxidase inhibitors drugs should be strongly reco

218 ase specific for spermine and spermidine and diamine oxidase specific for putrescine, were co-immobil

219 how specificity for VAP-1 over monoamine and diamine oxidases.

220 M = (N1,N1,N2,N2-tetramethylcyclohexane-1,2-diamine)Pd(NO(3))(2)] have been used to design enantiopu

221 The structure of diamine precursor 6 is characterized by high-field (1)H

222 Polyamines and their diamine precursor putrescine are ubiquitous to all organ

223 bic environment for a molybdenum diamine (Mo-diamine) precursor solution, enabling direct growth of i

224 synthesis of syn-1,2-aminoalcohol or syn-1,2-diamine precursors from a common terminal olefin has bee

225 ng graphitic nitrogen dopants induced by the diamine precursors, as demonstrated in mechanistic and c

226 of the free diazides in bulk solution yields diamine products.

227 h the formation of a range of differentiated diamine products.

228 itive zebrafish olfactory receptor for these diamines provides a molecular basis for studying neural

229 that combines aryl halides, isocyanides, and diamines provides access to 2-aryl-2-imidazolines in yie

230 Herein, we report an alkyne-appended cis-diamine Pt(II) compound, cis-[Pt(2-(5-hexynyl)amido-1,3-

231 Diamine putrescine (Put) and polyamines; spermidine (Spd

232 auA4, and pauA5 was found to be inducible by diamines putrescine (PUT) and cadaverine (CAD) but not b

233 ell is mainly carried by two small aliphatic diamines, putrescine and cadaverine, which are generated

234 phosphine, N,N,N',N'-tetramethylbutylene-1,4-diamine, pyridine, N,N,N',N'-tetramethylethylene-1,2-dia

235 (R-NOBIN) from (R)-(+)-1,1'-binaphthyl-2,2'-diamine (R-BINAM) is reported.

236 MSO clearly shows that in the monoprotonated diamines R2N(CH2)nN(+)R2H remote C-H deactivation can be

237 -6-44)-acetatodichlorido(cyclohexane-1 R,2 R-diamine)( rac-2-(2-propynyl)octanoato)platinum(IV) showe

238 -6-44)-acetatodichlorido(cyclohexane-1 R,2 R-diamine)( rac-2-(2-propynyl)octanoato)platinum(IV), are

239 tranitrate), HMTD (hexamethylene triperoxide diamine), RDX (hexogen), tetryl (2,4,6-trinitrophenylmet

240 p(3.32)) or V (non-canonical Asp(5.42)), and diamine receptors contain both aspartates.

241 ow that the proximity of the fluorine to the diamine ring hinders the dihedral angle rotation between

242 tabilization with a nearby charged site; the diamine ring of benzyl piperazine provided this charge s

243 nd p-fluorophenyl piperazine) containing the diamine ring structure and a fluorine atom were subseque

244 l angle rotation between the benzene and the diamine ring; this may partially account for the observe

245 ed their central core with benzothiazole-2,6-diamine scaffold and interchanged substituents in positi

246 n ancestral TAAR acquired Asp(5.42), gaining diamine sensitivity, and subsequently lost Asp(3.32).

247 y analysis indicates TAAR13c to be a general diamine sensor, with pronounced selectivity for odd chai

248 omer of the scarcely available and expensive diamine sparteine; also, these building blocks, together

249 Small modifications to the diamine structure are found to shift the threshold press

250 l shifts provides evidence in support of the diamine structure.

251 f all stereoisomers of spiro[3.3]heptane-1,6-diamines suitably protected for use as building blocks i

252 indered N-alkyl groups), and use of a novel "diamine switch" strategy to improve enantioselectivity w

253 A novel and practical chiral ruthenium-NHC-diamine system is disclosed for the enantioselective hyd

254 multifunctional C2-symmetric biphenyl-based diamine-tethered bis(thiourea) organocatalyst, which was

255 vels of antioxidant [gallic acid or ethylene diamine tetraacetate (EDTA)] in a sunflower oil salad dr

256 Ethylene diamine tetraacetic acid (EDTA), a chelating agent, can

257 , we report the anionic surfactant, ethylene diamine tetraacetic acid (EDTA), mediated synthesis of W

258 etic acid (Fe-DTPA) and of trans-cyclohexane diamine tetraacetic acid (Fe-tCDTA) were synthesized wit

259 ethylene diamine tetraacetic acid and serum dilution improved the

260 to detect high-level IgG, and after ethylene diamine tetraacetic acid treatment to obviate complement

261 is prospective study compared 177Lu-ethylene diamine tetramethylene phosphonate (EDTMP) with 153Sm-ED

262 , and even discriminate between two biogenic diamines that are selectively detected over monoamines a

263 ion for the preparation of the corresponding diamines that could be only obtained in good yield using

264 ne (5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine) that contribute to its inhibitory activity (IC5

265 ine (4-N-(6-methoxyquinolin-8-yl)pentane-1,4-diamine), the only drug that can block Plasmodium transm

266 In an effort to expand the library of such diamines, the synthesis and resolution of the C(2)-symme

267 his context, the asymmetric synthesis of 1,2-diamines through amination of enecarbamates has been pro

268 xcellent yield by replacing the amine with a diamine, thus showing the suitability of the system for

269 Switching from diamine to ethereal ligands inverts the sense of asymmet

270 iso)cyanate-containing polymers reacted with diamines to afford high-molecular-weight polymers with t

271 ther ethylene glycol oligomeric or polymeric diamines to yield bis-sulfonamides with short or long (p

272 d N3,N3,N6,N6-tetra-p-tolyl-9H-carbazole-3,6-diamine (TTAC).

273 iferromagnetically coupled singlet diradical diamine type ligands are described.

274 based on an oligo(phenylenethynylene) (OPE) diamine using a scanning tunneling microscope at room te

275 direct and selective assembly of vicinal 1,2-diamines using readily available olefin and amine buildi

276 determination of the binding constant to the diamine via luminescence quenching.

277 The synthesis of 1,2-diamines via a Rh-catalyzed intermolecular hydroaminatio

278 -methyl-5-(3-morpholinopropyl)pyrimidine-2,4-diamine was found to be a very potent dual TLR7/TLR8 ago

279 By contrast, an isomeric pyrene-based diamine was observed to undergo narcissistic self-sortin

280 n of aldehydes as the key step where syn-1,3-diamine was obtained as the most favorable product.

281 The formation of the desired diamines was found to be improved in the absence of base

282 ylthio)aniline, and N',N'-dimethylethane-1,2-diamine were found to undergo an efficient direct bis-ar

283 igoureas (up to n=6) of meso cyclohexane-1,2-diamine were synthesized by chain extension with an enzy

284 reactions of phosphinic chlorides with alkyl diamines were developed for the practical synthesis of u

285 ceI mediates the efflux of these short-chain diamines when energized by an electrochemical gradient.

286 ntral core (7H-pyrrolo[3,2-f]quinazoline-1,3-diamine), which may significantly expand the chemical sp

287 doamines are versatile precursors to vicinal diamines, which are among the most common motifs in biol

288 ensation reactions of substituted aromatic o-diamines with 1,2-naphthoquinone and 1,2-anthraquinone i

289 ic acids, hydroxy acids, amino alcohols, and diamines with an auxiliary-free cobalt probe.

290 The efficiency of tertiary diamines with different lengths of alkyl chain was exami

291 dine ring yields functionalized 1,2- and 1,3-diamines with high regioselectivity.

292 id-liquid conditions the condensation of the diamines with isophthalaldehyde or terephthaldehyde affo

293 n of N(2),N(4)-disubstituted quinazoline-2,4-diamines with minimum inhibitory concentrations (MICs) i

294 nd cleavage provided the N,N-diprotected 1,2-diamines with no loss in diastereo- or enantioselectivit

295 iation in the cyclocondensation of these 1,2-diamines with orthoesters.

296 her synthesis resulted in two types of spiro diamines, with varying substituents at both nitrogen ato

297 [tmeda = N, N, N', N'-tetramethylethane-1,2-diamine] with a symmetric tetraimidazole donor (L, 3,3',

298 hiles, leading to various 1-(hetero)aryl-1,2-diamines without loss of enantioselectivity and with com

299 (M) [tmeda = N,N,N',N'-tetramethylethane-1,2-diamine] yielded a complex mixture of stereoisomers of a

300 with benzene-1,4-diamine or with benzene-1,3-diamine yields the corresponding N,N'-(phenylene)bisphth