ライフサイエンスコーパス: diamine

1 tivity at another when treated with a chiral diamine.

2 of N,N'-bis(naphthalen-1-ylmethyl)ethane-1,2-diamine.

3 ccessible with a copper complex of O'Brien's diamine.

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

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

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

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

8 -amino amide or reduced to the corresponding diamine.

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

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

11 rivatives and a twisted conformation for the diamines.

12 ine affords differentially protected vicinal diamines.

13 gates and complexes with several widely used diamines.

14 tereoselective fluorescent sensor for chiral diamines.

15 of sparse olfactory sensory neurons by these diamines.

16 tracts, a physiologically relevant source of diamines.

17 sively as bis-solvated dimers with chelating diamines.

18 extrusion provided synthetically useful 1,2-diamines.

19 ay be converted to alpha-amino esters or 1,2-diamines.

20 cids, proline homologues, and cyclic vicinal diamines.

21 ld be reduced to give spirocyclic amines and diamines.

22 creasing yields, for the preparation of aryl diamines.

23 uction leads to stereochemically defined 1,2-diamines.

24 nt access to chiral ortho-substituted biaryl diamines.

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

26 clic tetraimines based on bis-alkynylbenzene diamines.

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

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

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

30 Diamines 1 were obtained by metal-mediated amine condens

31 itution reaction with methylamine to provide diamine 14 with inversion of configuration at the 1'-pos

32 thyl-N(4)-(pyridin-2-ylmethylene)benzene-1,4-diamine (2) were prepared and characterized.

33 -2-(2-furanyl) thiazolo[5,4-d]pyrimidine-5,7-diamines (2-18) and their pharmacological characterizati

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

35 , 8,9-disubstituted-3,9-dihydro-2H-purin-2,6-diamines 21-24 and 6-imino-1-phenyl-8,9-disubstituted-6,

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

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

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

39 ryl)benzaldehyde 3 with various amines 4 and diamines 5.

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

41 on provided differentially protected vicinal diamines 7 in good yield (80-91%).

42 es 5 (five examples) were reduced to vicinal diamines 7 with zinc hydrochloride; concomitant acyl mig

43 By employing a particular diamine, a closed-loop molecular pentafoil knot was prep

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

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

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

47 (5,6,7,8-tetrahydroquinolin-8-yl)but ane-1,4-diamine (AMD070) 2 as a potent and selective antagonist

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

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

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

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

52 yrosine and tryptophan residues to phenylene diamine and anisidine derivatives.

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

54 The condensation of linear diamine and dialdehyde subcomponents around copper(I) te

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

56 mpetitive inhibitors N,N'-dibenzylbutane-1,4-diamine and spermidine show that the fully protonated fo

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

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

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

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 ntly developed a novel oxidative coupling of diamines and isocyanides furnishing valuable guanidine-c

63 5,6,7-tetrahydro-N6-propyl-2,6-benzothiazole-diamine) and cyclosporine A (CSA) inhibited increases in

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

65 s with one primary and one secondary amines (Diamine) and triamine with one primary and two secondary

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

67 e, TMEDA = N,N,N',N'-tetramethylethylene-1,2-diamine, and PMDETA = N,N,N',N",N"-pentamethyldiethylene

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

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

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

71 aponification, condensation with symmetrical diamines, and deprotection.

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

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

74 Vicinal diamines are a common structural motif in bioactive natu

75 Urinary diamines are biomarkers of diisocyanate exposure.

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

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

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

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

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

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

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

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

84 urred exclusively at the nitrogen using a Cu-diamine-based catalyst system.

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

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

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

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

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

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

91 converted into mono-benzyl-protected vicinal diamines by the reduction with aluminum hydride.

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

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

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

95 ng bulky counteranion, a cationic Cp*Rh(III)-diamine catalyst displayed excellent enantioselectivitie

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

97 Four vicinal diamine-catalyzed aldol reactions were examined.

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

99 iflic acid salt of the completely deuterated diamine (CD3)2N(CD2)4N(CD3)2.

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

101 d by the cooperative catalysis of an Ir(III)-diamine complex and a chiral phosphoric acid or its conj

102 oximately 350 nm is assigned as either a gem-diamine complex or a thiol adduct formed by nucleophilic

103 deprotonation reactions using organolithium/diamine complexes in THF.

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

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

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

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

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

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

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

111 N2,N4-dibenzylquinazoline-2,4-diamine (DBeQ) was identified as a selective, potent, re

112 hrough reactivity with N,N-dibutyl phenylene diamine (DBPDA), which leads to the formation of a fluor

113 = La and Eu; DMEDA = N, N'-dimethylethylene diamine] demonstrate binding of these Lewis basic substr

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

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

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

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

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

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

120 -HCV activity, we identified a family of 1,2-diamines derived from trans-stilbene oxide that prevent

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

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

123 acer, N'1'-(4-methylquinolin-2-yl)ethane-1,2-diamine dinitrate, was employed to study the effects of

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

125 monoimines formed with aliphatic alpha,omega-diamines display an internal exchange process of self-tr

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

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

128 We discovered that a short ethylene diamine (Et) linker displayed high cellular permeability

129 -butylhydroxybenzyl)-1,2-cyclohexane-(1R,2R)-diamine) exists as a temperature-invariant Cu(II)-ligand

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

131 s, this systematic review asked: Will silver diamine fluoride (SDF) more effectively prevent caries t

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

133 , (iii) quantification of methylene diphenyl diamine following acid hydrolysis, and (iv) immunoassay.

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

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

136 the methyl-substituted lithiated carbamate, diamine-free conditions were required to achieve high se

137 A new diamine-functionalized metal-organic framework comprised

138 rotein 90 inhibitor 17-N,N-dimethyl ethylene diamine-geldanamycin in vivo.

139 Both (-)-sparteine and O'Brien's diamine give higher optical purities with VANOL and VAPO

140 s, presumably via its nitrogen atoms on PANI/diamine groups.

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

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

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

144 A series of monoprotonated aliphatic diamines has been examined, which crystallize in three g

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

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

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

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

149 trometry (IRMS) on hexamethylene triperoxide diamine (HMTD) and its precursor hexamethylenetetramine

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

151 etranitrate (HMX), hexamethylene triperoxide diamine (HMTD), 2,4-dinitrotoluene, 1,3-dinitrobenzene,

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

153 quantification of hexamethylene triperoxide diamine (HMTD), which is one of commonly used explosives

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

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

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

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

158 nt drug intermediate (R)-3-phenylpropane-1,2-diamine in high yield with high enantioselectivity.

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

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

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

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

163 5,6,7-tetrahydro-N6-propyl-2,6-benzothiazole-diamine) in subjects with ALS in a two-part, double-blin

164 4'-methyl-N(2)-phenyl-[4,5'-bithiazole]-2,2'-diamine inhibitors of gyrase B with a low micromolar inh

165 els of enantioselectivity in the presence of diamine inhibitors.

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

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

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

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

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

171 [(2-methoxyphenyl)-methyl]hexyl]-1,8-octane] diamine) is an M(2)-selective competitive antagonist of

172 -13 dendrimer comprising triazines linked by diamines, is stable across ranges of concentration, pH,

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

174 1000 used previously in some researches and diamine Jeffamine ED-2003 applied for the first time for

175 imethyl-N(4)-(pyridin-2-ylmethyl)benzene-1,4-diamine (L2-b) that can interact with both metal ions an

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

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

178 y 4,5-pinenopyridine donor ligands, a chiral diamine ligand backbone, and chirality at the metal (Lam

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

180 zed by reacting the Cu(I) complex of the bis-diamine ligand N,N'-di-tert-butyl-ethylenediamine (DBED)

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

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

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

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

185 by cross-linking with alkyne-functionalized diamine linker that allows for the conjugation of azide-

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

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

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

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

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

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

192 ound to be very poor catalysts, whereas some diamines, most notably ethylenediamine, were excellent c

193 incorporation of a diverse range of achiral diamine motifs.

194 opic salts of some high performance ligands (diamine MsOH salts/CuX and copper(II) diketonates) were

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

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

197 R(2))H, which are useful precursors for N,N'-diamines, N-heterocyclic carbenes, and other heterocycle

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

199 (1-naphthyl)N,N'-diphenyl-1,1'-biphenyl-4,4'-diamine (NPB) and lowest unoccupied molecular orbital (L

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

201 Replacement of ethanolamine with ethylene diamine or 1,3-diaminopropane in these reactions resulte

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 d cannot be prevented through refrigeration, diamine oxidase (DAO) enzyme may be used to degrade hist

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

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

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

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

211 6, P = 0.04205), and intracellularly labeled diamine oxidase (P = 0.0003, P = 0.0148).

212 is not a substrate of either porcine kidney diamine oxidase (pkDAO) or rat liver monoamine oxidase (

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

214 minobutyraldehyde with putrescine oxidase or diamine oxidase as catalysts.

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

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

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

218 yte cytochrome-c oxidase; total glutathione; diamine oxidase; and urinary pyridinoline.

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

220 -13) were used to enumerate analogues of the diamine part of two known alpha7 nicotinic receptor agon

221 , a bis-trimethylene bridged bis-p-phenylene diamine (PD), and its ethyl and isopropyl analogues are

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

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

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

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

226 ction furnish differentially substituted 1,2-diamine products.

227 of the free diazides in bulk solution yields 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 ynthesis of the triamine spermidine from the diamine putrescine by fusion enzymes from beta-proteobac

233 nt of a transporter capable of exporting the diamine putrescine in the Chinese hamster ovary (CHO) ce

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

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

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

237 abstraction reactions from cyclic amines and diamines (pyrrolidines, piperidines, morpholines, and pi

238 A library of diamine quinoline methanols were designed based on the m

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

240 up from two (P)-2 linked together with three diamines (R)-5.

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

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

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

244 The TunePhos/diamine-Ru(II) complex combined with t-BuOK in 2-propano

245 ,13,16,19-hexaazabicyclo[6.6.6]-eicosane-1,8-diamine) (SarAr) chelator to bombesin(7-14), radiolabel

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

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

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

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

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

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

252 the periodate-mediated reaction of phenylene diamine substituted oligonucleotides with aniline groups

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

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

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

256 ibit this background reaction, the chelating diamine TEEDA (tetraethylethylene diamine) was introduce

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

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

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

260 ethylene diamine tetraacetic acid and serum dilution improved the

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

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

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

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

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

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

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

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

271 ulting oligoribonucleotide product using 1,2-diamines under anhydrous conditions.

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

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

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

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

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

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

278 The desymmetrization of meso-diamines was accomplished via enantioselective monobenzo

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

280 chelating diamine TEEDA (tetraethylethylene diamine) was introduced prior to aldehyde addition.

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

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

283 In total, 21 diamines were prepared and acylated with aromatic carbox

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

285 is(2-methoxyethyl)-N(2),3-dimethylbutane-1,2-diamine, which is a chiral amide base synthesized from (

286 ps under basic conditions furnishes the free diamines, which should find broad utility in asymmetric

287 ediate 5-chloro-9H-pyrimido[4,5-b]indole-2,4-diamine with appropriate benzenethiols.

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

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

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

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

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

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

294 ary and secondary monoamines (pMono, sMono), diamines with one primary and one secondary amines (Diam

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

296 hed and mismatched copper complexes of these diamines with the biaryl ligands.

297 t-butylsalicylidene)-1,2-cyclohexane-(1R,2R)-diamine) with a non-innocent salen ligand has been inves

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

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

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