ライフサイエンスコーパス: triazine

1 f MNX (hexahydro-1-nitroso-3,5-dinitro-1,3,5-triazine).

2 DLLME-SFO) was developed for the analysis of triazines.

3 es, pyrazines, pyrimidines, pyridazines, and triazines.

4 the triazine to provide imidazo[1,2-a][1,3,5]triazines.

5 he impact is of a magnitude to convert 1,2,3-triazine (1) and its modest cycloaddition scope into a h

6 um, and potassium salts of 2,4,6-trimethyl-s-triazine (1) with 2-halomethyl-4,6-dimethyl-s-triazine (

7 of 2-amino-4-cyanopyrroles (3a-e) with 1,3,5-triazines (1, 2) is reported.

8 ,2,4,5-tetrazines; 1,2,4-, 1,3,5-, and 1,2,3-triazines; 1,2-diazines; and 1,3,4-oxadiazoles), 1-aza-1

9 4-triazol-5-ylm ethoxy)pyrazolo[1,5-d][1,2,4]triazine (13) has been identified as a functionally sele

10 heny l]-1H-pyrazol-4-yl}imidazo[5,1-f][1,2,4]triazine, [(18)F]PF-05270430 (5).

11 rom 3-chloro- (1c) and 3-iodobenzo[ e][1,2,4]triazine (1d) obtained in three steps from 2-nitroanilin

12 The selectively (15)N labeled azido-1,2,4-triazine 2*A and azidopyrimidine 4*A were synthesized by

13 riazine (1) with 2-halomethyl-4,6-dimethyl-s-triazine (2) (X = Cl, Br) in glyme have been studied and

14 -3,3'-bicarbazole (BCzPh):3',3'",3'""-(1,3,5-triazine-2,4,6-triyl)tris(([1,1'-biphenyl]-3-carbonitril

15 )(TATB)(2), where TATB represents 4,4',4''-s-triazine-2,4,6-triyl-tribenzoate with a formula of C(24)

16 ng a triazine-based planar ligand, 4,4',4"-s-triazine-2,4,6-triyltribenzoate (TATB) and mixed lanthan

17 trazine (6-Chloro-n-ethyl-n'-(1-methylethyl)-triazine-2,4-diamine), a prevalent herbicide in the Unit

18 of the side chain to the N,N-dimethyl-1,3,5-triazine-2,4-diamine-6-ethyl moiety by NMR spectroscopy,

19 hyl-2-oxazoline)-b-poly(2-N,N-dimethyl-1,3,5-triazine-2,4-diamine-6-ethyl-2-oxazoline) (PMeOx-PcBOx),

20 4-(N-phenylanilino)-6-pyrrolidin-1-yl-1,3,5-triazine-2-carbonitrile (CP243522), showed a K(i) of 21

21 m, 6-hydroxy-2-(naphthalen-1-ylmethyl)-1,2,4-triazine-3,5(2H,4H)-dione 11h was found to be selective

22 A series of 2-substituted 6-hydroxy-1,2,4-triazine-3,5(2H,4H)-dione derivatives were synthesized a

23 The 6-hydroxy-1,2,4-triazine-3,5(2H,4H)-dione pharmacophore appears metaboli

24 yl)piperazin-1-yl]butyl}-4- methyl-2H-[1,2,4]triazine-3,5-dione (10), a potential high affinity (K(i)

25 yl)piperazin-1-yl]butyl}-4-methyl-2H-[1,2,4 ]triazine-3,5-dione (9) and [(11)C]CH(3)OTf in 25 +/- 5%

26 use in promoting the cycloaddition of 1,2,3-triazine 4 with enamine 3 as the key step of a concise t

27 s 4-amino-3,7-dinitrotriazolo-[5,1-c][1,2,4] triazine 4-oxide (DPX-27), which is also predicted to be

28 synthesis of 3-methyl-5-phenylethynyl[1,2,4]triazine (4), 6-methyl-3-phenylethynyl[1,2,4]triazine (5

29 riazine; 4,4',6,6'-tetra(azido)hydrazo-1,3,5-triazine; 4,4',6,6'-tetra(azido)azo-1,3,5-triazine; and

30 compounds, for example, 2,4,6-triazido-1,3,5-triazine; 4,4',6,6'-tetra(azido)hydrazo-1,3,5-triazine;

31 triazine (4), 6-methyl-3-phenylethynyl[1,2,4]triazine (5), and 5-methyl-3-phenylethynyl[1,2,4]triazin

32 ture of 4-amino-7-benzylpyrrolo[2,3-d][1,2,3]triazine-5-carbonitrile (19) and 2-amino-1-benzylpyrrole

33 4-[1H-indazol-5-ylamino]pyrrolo[2,1-f][1,2,4]triazine-6-carbamates identified dual human epidermal gr

34 Lead optimization resulted in pyridinyl triazine 63, which exhibited >30-fold selectivity over a

35 zine (5), and 5-methyl-3-phenylethynyl[1,2,4]triazine (6a) as analogues of 2-methyl-6-(phenylethynyl)

36 ere 3-(3-methylphenylethynyl)-5-methyl[1,2,4]triazine (6b), 5-(3-chlorophenylethynyl)-5-methyl[1,2,4]

37 b), 5-(3-chlorophenylethynyl)-5-methyl[1,2,4]triazine (6c), and 3-(3-bromophenylethynyl)-5-methyl[1,2

38 and 3-(3-bromophenylethynyl)-5-methyl[1,2,4]triazine (6d).

39 -thiadiazole (4), phenyl- and diphenyl-1,3,5-triazines (7 and 8), and a trace quantity of diphenyl-1,

40 ighly sensitive functional groups, such as a triazine, a ketone, an aldehyde, or a nitro group, were

41 2-Azido-4,6-dimethoxy-1,3,5-triazine (ADT) was reported recently as a new "intrinsic

42 novel 2,7-disubstituted pyrrolo[2,1-f][1,2,4]triazine ALK inhibitors are described along with synthes

43 Trifluoro-1,3,5-triazine also participates in aryl centroid complexation

44 razines derivatives of [1,2,4]triazolo[1,5-a]triazine also possessed good oral efficacy in rodent mod

45 re, functional analysis of aminophenyl-1,3,5-triazine analogs elucidated structure-activity relations

46 along with X-ray structures with a series of triazine analogues aids in deciphering the mechanism by

47 nM) confirmed that the pyrrolo[2,1-f][1,2,4]triazine analogues are competitive with ATP.

48 Therefore, we have synthesized a triazine and a keto functionalized nonmetal based covale

49 was modified with 2,6-diamino-4-phenil-1,3,5-triazine and characterized by FTIR, SEM and elemental an

50 etween 1,3,5-tris(2-hydroxyethyl)hexahydro-s-triazine and hydrogen sulphide, the principle by-product

51 etween 1,3,5-tris(2-hydroxyethyl)hexahydro-s-triazine and hydrogen sulphide, to be measured for a spe

52 cted from among industrial chemicals and the triazine and phenoxyacetic acid herbicide classes.

53 ecular coordination complexes (SCCs) bearing triazine and porphyrin faces with promising light-harves

54 nitio study of the interaction between 1,3,5-triazine and the fluoride, chloride, and azide ion at th

55 mplexes between a star-shaped tris(triazolyl)triazine and triphenylene-containing benzoic acids is de

56 n family, from a conveniently prepared 1,2,4-triazine and via a common tetrasubstituted pyridine inte

57 zadiene, complementary to the isomeric 1,2,4-triazines and 1,3,5-triazines, capable of dependable par

58 between substituted electron-deficient 1,2,3-triazines and a highly functionalized and chiral primary

59 six pyridinium rings fused with two central triazines and bridged by three paraxylylene units.

60 Both furo[3,4-d][1,2,3]triazines and dihydrotriazines exhibit good fluorescence

61 nisms of Diels-Alder reactions between 1,2,3-triazines and enamines have been explored with density f

62 Reactions between substituted 1,2,4-triazines and ketones were investigated.

63 y cocrystal structures of KDR inhibitors 34 (triazine) and 35 (nicotinamide).

64 ntaining RDX (hexahydro-1,3,5-trinitro-1,3,5-Triazine) and HMX (octahydro-1,3,5,7-tetranitro-1,3,5,7-

65 yl-oxazoles, -thiazoles, -imidazoles, -1,2,4-triazines, and -pyridines are available from the diazoke

66 ectron-demand Diels-Alder reactions of 1,2,3-triazines, and that these mechanisms can be altered by e

67 olyzed other N-substituted amino dihydroxy-s-triazines, and those with linear N-alkyl groups had high

68 azabenzenes (pyridine, three diazines, three triazines, and three tetrazines) with the ethylene dieno

69 ,5-triazine; 4,4',6,6'-tetra(azido)azo-1,3,5-triazine; and 2,5,8-tri(azido)-1,3,4,6,7,9,9b-heptaazaph

70 diazine, 1,3-diazine, 1,4-diazine, and 1,3,5-triazine are 110.4 +/- 2.0, 111.3 +/- 0.7, 113.4 +/- 0.7

71 ne, and dicyclopenta[b,d]pyrido[1,2-f][1,2,4]triazine are described.

72 2-Hydroxy-4,6-diamino-[1,3,5]triazines are described which are a novel class of poten

73 , neutral and basic pesticides (phenylureas, triazines) are more sensitive using APCI (especially pos

74 r studies demonstrate the versatility of the triazine as a modular scaffold to generate potent and se

75 Here we present the trifunctionalized 1,3,5-triazine as an ideal modular scaffold for generating lib

76 sing C3-symmetric 2,4,6-tri(4-pyridyl)-1,3,5-triazine as pore-partition agent in MIL-88 type (the acs

77 tin as the tumor-targeting moiety, and 1,3,5-triazine as the tripod splitter module, were designed an

78 common synthon affording access to pyridinyl triazines as the 4,4'-amino derivatives which are commer

79 ichael addition to substituted 3-vinyl-1,2,4-triazines, as original bifunctional platforms for the do

80 no-1,3,5-triazine with 2,4,6-trichloro-1,3,5-triazine at 1.0-1.5 GPa and 500-550 degrees C and also t

81 self-reaction of 2-amino-4,6-dichloro-1,3,5-triazine at similar conditions.

82 2-chloro-4-ethylamino-6-isopropylamino-1,3,5-triazine (atrazine), 2.4-dichlorophenoxyacetic acid (2,4

83 mical genetic screenings were performed with triazine-based combinatorial libraries that include vari

84 Two triazine-based dendrimers were successfully prepared in

85 bottlebrush nanofibers from an acridine- and triazine-based donor/acceptor pair, which have been show

86 A series of 1,3,5-triazine-based estrogen receptor (ER) modulators that ar

87 Porous, fluorescent, covalent triazine-based frameworks (CTFs) are obtained in an unpr

88 fluoro-1H-indol-5-yloxy)pyrrolo[2,1-f][1,2,4]triazine-based inhibitors of vascular endothelial growth

89 Novel triazine-based microtubule inhibitors were discovered by

90 Triazine-based nanosheets are 1-2 nm in height and affor

91 ch rapidly isomerizes to a 3,4-dihydro-1,2,4-triazine-based nitrone, namely 6-phenyl-3-pyridin-2-yl-2

92 imiralisib), a potent 4,6-dimorpholino-1,3,5-triazine-based pan-class I PI3K inhibitor, which targets

93 -organic frameworks were synthesized using a triazine-based planar ligand, 4,4',4"-s-triazine-2,4,6-t

94 activation chemistry was developed using the triazine-based reagent 4-(4,6-dimethoxy (1,3,5)triazin-2

95 eton for forming these bivalent compounds is triazine-based.

96 s as the point of intersection of multiple s-triazine biodegradative pathways and is completely essen

97 xplosive RDX (hexahydro-1,3,5-trinitro-1,3,5-triazine) by microorganisms involves sequential reductio

98 The synthesis of a pyrazolo[1,5-a]-1,3,5-triazine C-nucleoside (dA(PT)), designed to form two hyd

99 tether from the imidazole N1 position to the triazine C3 proceed in excellent yields to produce 1,2,3

100 ry to the isomeric 1,2,4-triazines and 1,3,5-triazines, capable of dependable participation in invers

101 four pesticide classes (chloroacetanilides, triazines, carbamates organophosphates) and two pesticid

102 Because of the presence of the acceptor (triazine) center and strong donors in the arms (diarylam

103 high-throughput screening, aminophenyl-1,3,5-triazine CFTRact-K089 (1) that activated CFTR with EC50

104 An aminophenyl-1,3,5-triazine, CFTRact-K089, fully activated CFTR in cell cul

105 ies that act on the commercially important s-triazine class of compounds.

106 with the recent introduction of industrial s-triazine compounds such as atrazine and melamine into th

107 Organophosphates, triazoles, pyrethroids and triazines compounds showed good linearity in the range 0

108 salts) was developed and led to the desired triazines compounds, thus allowing a one-step economy in

109 t the 6-position of the pyrrolo[2,1-f][1,2,4]triazine core gave potent compounds.

110 This [1,2,4]triazolo[1,5-a]triazine core structure has now been improved by incorpo

111 ster substituent of the pyrrolo[2,1-f][1,2,4]triazine core with heterocyclic bioisosteres, such as su

112 cules consist of an electron-deficient 1,3,5-triazine core with three fluorene arms substituted with

113 ative reactions of the growing dendrons with triazine cores and diamine linkers.

114 8-(substituted pyridyl)pyrazolo[1,5-a]-1,3,5-triazine corticotropin releasing factor receptor-1 (CRF(

115 of 8-(4-methoxyphenyl)pyrazolo[1,5-a]-1,3,5-triazine corticotropin releasing factor receptor-1 (CRF(

116 r, TCT hydrolyzes to 2,4-dicyano-6-hydroxy-s-triazine, DCTOH.

117 iterative synthesis of a second generation, triazine dendrimer with 12 protected amines on the perip

118 and host-guest chemistry of high-generation triazine dendrimers are described.

119 ed that the guest capacity of odd-generation triazine dendrimers increased until generation 7 but dec

120 benzene-functionalized high-molecular weight triazine dendrimers up to generation 9, demonstrating th

121 The redox active 1,3,5-triazine derivative (MPT) was used as a guest to study h

122 The [1,2,4]triazolo[1,5-a]triazine derivative 3, more commonly known in the field

123 itrile and aromatization to generate a 1,2,4-triazine derivative.

124 onversion of new carboxamides (5 and 6) to s-triazine derivatives (7) was demonstrated in mouse and h

125 fluorinated nitrile 1e was converted to the triazine derivatives 2a and 2b by catalysis with Ag(2)O

126 The results suggest the metabolites, s-triazine derivatives 7, may be the active species of the

127 ent, selective, and orally efficacious 1,2,4-triazine derivatives have been identified using structur

128 A series of bis(morpholino-1,3,5-triazine) derivatives were prepared and optimized to pro

129 Length-monodisperse triazine-derivatized polymers were prepared on gram-scal

130 The effectiveness of novel sym-triazine-derived aggregation modulators (TAE-1, TAE-2) t

131 (6-ethynyl-pyridin-2-yl)-5,6-diphenyl-[1,2,4]triazine dipolarophiles with structurally diverse 4-meth

132 ound and the desired fused tricyclic 1,2,3,4-triazine display interesting thermal behavior and are pr

133 rate salts with a 1,3,5-tris(dipicolylamine)-triazine (dpat) ligand yielded two unprecedented example

134 d 4-amino-3,7-dinitrotriazolo-[5,1-c][1,2,4] triazine (DPX-26).

135 The excited-state dynamics of an aniline-triazine electron donor-acceptor dyad with an alkyne spa

136 in that it contains an amine reactive group (triazine ester) targeting the N-terminus and epsilon-ami

137 ing groups (-CO2R) at C4 and C6 of the 1,2,3-triazine even if C5 is unsubstituted (Me or H), highligh

138 lass 3a carcinogen, is a pesticide of chloro triazine family and is known to severely affect the huma

139 Covalent triazine frameworks (CTFs) are normally synthesized by i

140 mily of hexaazatriphenylene-based conjugated triazine frameworks (CTFs) for efficient CO2 capture.

141 The synthesis of highly crystalline covalent triazine frameworks (CTFs) with ultrastrong covalent bon

142 ic frameworks, microporous polymer, covalent triazine frameworks etc.) and their heterostructures.

143 ed, but not eliminated, by the withdrawal of triazines from conventional maize cropping.

144 ching of RDX (hexahydro-1,3,5-trinitro-1,3,5-triazine) from particulates deposited in live-fire milit

145 ractions upon binding to the kinases via its triazine functional group, which is considerably larger

146 bis[hydroxy(methyl)amino]-4-morpholino-1,3,5-triazine (H(2)BHT).

147 ituted 4-(phenylamino)-pyrrolo[2,1- f][1,2,4]triazines has been discovered.

148 this series of [1,2,4]triazolo[1,5-a][1,3,5]triazine have now been shown to be orally active in the

149 s piperazine series of [1,2,4]triazolo[1,5-a]triazine have now been shown to have good oral bioavaila

150 ves of 2-furanyl[1,2,4]triazolo[1,5-a][1,3,5]triazine have recently been demonstrated to be potent an

151 ric 2-(hydroxytolyl)-4,6-dimethylamino-1,3,5-triazines have been synthesized in high yields in a cont

152 rse electron-demand Diels-Alder reactions of triazines have wide applications in bioorthogonal chemis

153 o been applied to the preparation of a 1,3,5-triazine having three different substituents.

154 Here, we forecast weed abundances in post-triazine herbicide regimes.

155 s insecticides, phenoxy-acid herbicides, and triazine herbicide) to inhibit butyrylcholinesterase, al

156 s-Triazine herbicides (atrazine, ametryn) are groundwater

157 Withdrawal of the triazine herbicides atrazine, simazine and cyanazine fro

158 hine and propaphenone in untreated urine and triazine herbicides in a soil extract.

159 Here we analyse effects of applications of triazine herbicides in conventional maize regimes on key

160 evelopment of time and location profiles for triazine herbicides in environmental samples.

161 As model compounds four selected triazine herbicides namely, simazine, atrazine, secbumet

162 eference adsorbent graphite was conducted of triazine herbicides, substituted anilines, heterocyclic

163 nce and trematode exposure was observed with triazine herbicides, this effect was driven by increases

164 mpletely essential for microbial growth on s-triazine herbicides.

165 e four FSE sites analysed that used only non-triazine herbicides.

166 ediates generated during the metabolism of s-triazine herbicides.

167 ling reaction, were used to assemble various triazine-heteroaryl analogues effectively.

168 phenylene vinylene) derivative with a ureido-triazine hydrogen bonding unit self-assembles into rows

169 ring nitrogen was protonated in the enzyme s-triazine hydrolase (TrzN) where (iii) TrzN crystal struc

170 TrzN, the broad-specificity triazine hydrolase from Arthrobacter and Nocardioides sp

171 Atrazine chlorohydrolase, TrzN (triazine hydrolase or atrazine chlorohydrolase 2), initi

172 ionation pattern for identifying microbial s-triazine hydrolysis in the environment caused by multipl

173 amino acids, sugars, organic acids, amides, triazine, imidazole, protein, and biological tissue.

174 synthesis of the layered bulk material poly(triazine imide), PTI, followed by one-step liquid exfoli

175 rrole with 2,4,6-tris(trifluoromethyl)-1,3,5-triazine in THF-d(8) to give a pyrrolo[2,3-d]pyrimidine

176 erized by NMR and MS and was identified as a triazine in which the pyrimidine ring was oxidatively de

177 cient methodology for the synthesis of 1,3,5-triazines in good to excellent yields under transition-m

178 synthesis of highly fused furo[3,4-d][1,2,3]triazines in good-to-excellent yields under mild conditi

179 form 2,4-disusbstituted-6-substituted 1,3,5-triazines in moderate to good yields.

180 Dispersion (MSPD) for determination of nine triazines in mussels has been optimised in terms of the

181 xplosive RDX (hexahydro-1,3,5-trinitro-1,3,5-triazine) in an aquifer near the Iowa Army Ammunition Pl

182 henyl)-1H-p yrazol-4-yl)imidazo[1,5-f][1,2,4]triazine, in nonhuman primates.

183 ectron demand Diels-Alder reactions of 1,2,3-triazines is disclosed, including an examination of the

184 A new class of bioorthogonal reagents, 1,2,4-triazines, is described.

185 dyl-based ligands, 2,4,6-tri-4-pyridyl-1,3,5-triazine (L1) and 5,10,15,20-tetra(4-pyridyl)-21H,23H-po

186 aled that the oxindole-pyrrolo[2,1- f][1,2,4]triazine lead 2a displayed potent enzyme inhibition (IC

187 nal combinatorial synthesis of a high-purity triazine library was demonstrated.

188 ibition of regeneration, we screened a novel triazine library, based on the ability of compounds to i

189 y a phenanthroline-derived quadridentate bis-triazine ligand are described.

190 first 1:2 bis-complex of a quadridentate bis-triazine ligand to be characterized by crystallography.

191 trong covalent bonds (aromatic C N) from the triazine linkage presents a great challenge to synthetic

192 -Alder reaction between imidazoles and 1,2,4-triazines linked by a trimethylene tether from the imida

193 target, a generation-13 dendrimer comprising triazines linked by diamines, is stable across ranges of

194 nctional monomer (2,4,6-trisacrylamido-1,3,5-triazine), mixed templates (ascorbic acid and dopamine),

195 on reaction revealed that the inherent 1,2,3-triazine mode of cycloaddition (C4/N1 vs C5/N2) as well

196 Simple organic cooperative assembly of triazine molecules leads to three-dimensional macroscopi

197 lamino)-4-hydroxy-6-(N-isopropylamino)-1,3,5-triazine] N-ethylaminohydrolase (AtzB) is the sole enzym

198 high-throughput screen of cruzain identified triazine nitriles, which are known inhibitors of other c

199 Hydrogen bonding between one of the triazine nitrogens and the backbone NH of the Met109 res

200 The pyrrolo[2,1-f][1,2,4]triazine nucleus was identified as a novel kinase inhibi

201 n nanoring to two tridentate ligands (with s-triazine or benzene cores) occurs with high negative all

202 of arylhydrazines, o-aminoacetophenones, and triazines or nitriles.

203 but not RDX (hexahydro-1,3,5-trinitro-1,3,5-triazine) or 2,6-DNT (2,6-dinitrotoluene).

204 ction initially produces a population of sym-triazine partitioned between the 3s Rydberg and pi* <--

205 pite stereoregio backbone heterogeneity, the triazine polymers bind T/U-rich DNA or RNA with nanomola

206 d and exothermic decomposition of a reactive triazine precursor, C 3N 3(NHCl) 3, was examined by bypr

207 2-substituted imidazoles with various 1,2,4-triazines produced both imidazo[4,5-c]pyridines (3-deaza

208 ducts, the suggested precursors of the 1,3,5-triazine products 7 and 8.

209 nd compound B led to the discovery of [1,3,5]triazine-pyridine as a new series of potent CDK inhibito

210 s induced by charge exchange between the sym-triazine radical cation and cesium.

211 es containing hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and 2,4,6-trinitrotoluene (TNT) from poly

212 ne compounds, hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and octahydro-1,3,5,7-tetranitro-1,3,5,7-

213 hmarks, such as 1,3,5-trinitroperhydro-1,3,5-triazine (RDX) and octahydro-1,3,5,7-tetranitro-1,3,5,7-

214 ively removes hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) from groundwater but generates RDX-laden

215 mines such as hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) have been updated with the insensitive mu

216 Hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) is a common constituent of military explo

217 1,3,5-Trinitroperhydro-1,3,5-triazine (RDX) is a principal component of plastic explo

218 Hexahydro-1,3,5-trinitro-1,3,5,-triazine (RDX) is a toxic and mobile groundwater contami

219 The explosive Hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) is known to be degraded aerobically by va

220 awing explosive 1,3,5-trinitroperhydro-1,3,5-triazine (RDX) produced no response.

221 losive molecule 1,3,5-trinitroperhydro-1,3,5-triazine (RDX) via combined nanomechanical photothermal

222 uene (TNT), and 1,3,5-trinitroperhydro-1,3,5-triazine (RDX)).

223 azocine (HMX), 1,3,5-trinitroper-hydro-1,3,5-triazine (RDX), 2,4,6-trinitrotoluene (TNT), 2-amino-4,6

224 rgetic compound 1,3,5-trinitroperhydro-1,3,5-triazine (RDX), a known neurotoxicant.

225 otoluene (TNT), 1,3,5-trinitroperhydro-1,3,5-triazine (RDX), and pentaerythritol tetranitrate (PETN)

226 oluene (TNT), hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), and pentaerythritol tetranitrate (PETN)

227 on of the explosives trinitrohexahydro-1,3,5-triazine (RDX), octahydro-1,3,5,7-tetranitro-1,3,5,7-tet

228 ermination of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), octahydro-1,3,5,7-tetranitro-1,3,5,7-tet

229 1,3,5-trinitroperhydro-1,3,5-triazine (RDX), octahydro-1,3,5,7-tetranitro-1,3,5,7-tet

230 nvironment of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), one of the most widely used military exp

231 oglycerin (NG), 1,3,5-trinitroperhydro-1,3,5-triazine (RDX), pentaerythritol tetranitrate (PETN), tri

232 ior to those of 1,3,5-trinitroperhydro-1,3,5-triazine (RDX).

233 ), and 0.3 mm hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX).

234 rior to that of 1,3,5-trinitroperhydro-1,3,5-triazine (RDX).

235 eacted 1,3,5-tris(2-hydroxyethyl)hexahydro-s-triazine remaining; the only source of inorganic sulphid

236 the terminal reaction during metabolism of s-triazine ring compounds by bacteria.

237 Stability of the triazine ring in aqueous solution was not improved in th

238 identification and (ii) suggested that the s-triazine ring nitrogen was protonated in the enzyme s-tr

239 alyze the sequential hydrolytic removal of s-triazine ring substituents from the herbicide atrazine t

240 The cleavage of the triazine ring under previously developed conditions1-6 r

241 electronic structure of the benzo[ e][1,2,4]triazine ring was investigated by spectroscopic methods

242 for formation of the 1,4-dihydrobenzo[1,2,4]triazine ring was investigated using the B3LYP/6-31G(2d,

243 Substrates required a monohydroxylated s-triazine ring with a minimum of one primary or secondary

244 ive complexes for nucleophilic attack on the triazine ring, and pi-stacking interactions (with azide)

245 Donor substituents were attached on the triazine ring, including pyrazolyl-substituted anilines

246 acement of a chlorine substituent from the s-triazine ring.

247 oducts arising from over-substitution of the triazine ring.

248 lane, covalent organic frameworks containing triazine rings (t-COFs) hold great promise in this regar

249 st compounds 5-methyl-3-phenylethynyl-[1,2,4]triazine (RTI-4229-707), 5-methyl-3-(4-phenoxy-phenyleth

250 , 5-methyl-3-(4-phenoxy-phenylethynyl-[1,2,4]triazine (RTI-4229-766), and 3-(3-methylphenylethynyl)-5

251 3-(2,5-dimethylphenylethynyl)-5-methyl[1,2,4]triazine (RTI-4229-785) and 3-(2-methylphenylethynyl)-5-

252 nd 3-(3-methylphenylethynyl)-5-methyl-[1,2,4]triazine (RTI-4229-787) resulted in a dose-dependent blo

253 and 3-(2-methylphenylethynyl)-5-methyl[1,2,4]triazine (RTI-4229-828) were totally inactive.

254 The enhanced stability of the triazine scaffold enabled its direct use in recombinant

255 novel 2,7-disubstituted-pyrrolo[2,1-f][1,2,4]triazine scaffold has been designed as a new kinase inhi

256 validation of this new pyrrolo[2,1-f][1,2,4]triazine scaffold will be described for inhibitors of an

257 n maps confirmed triphenylene/tris(triazolyl)triazine segregation into hexagonal sublattices and latt

258 side chain provides a proton to N-1 of the s-triazine substrate to facilitate nucleophilic displaceme

259 fferent relative activities with different s-triazine substrates.

260 ase had no detectable activity with the halo-triazine substrates.

261 zed to generate protonated 2,4,6-trimethyl-s-triazine tautomers in situ, which undergo Aldol condensa

262 The triazine-TCO reaction can also be used in tandem with ot

263 ent cyanuric chloride (2,4,6-trichloro-1,3,5-triazine, TCT) catalyzed approach for the synthesis of 2

264 Chemical reduction of 2,4,6-tricyano-1,3,5-triazine, TCT, results in the formation of an unstable r

265 ,6-trichloro-1,3,5-triazine were used--1,3,5-triazines that had leaving groups.

266 amorphous carbon nitride networks formed by triazine thermolysis reactions.

267 carbon nitride materials that are formed via triazine thermolysis.

268 TPT)(4) (TPT = 2,4,6-tri(pyridin-4-yl)-1,3,5-triazine), thus allowing for utilization of crystallogra

269 1, was made by linking 2,4,6-trimethyl-1,3,5-triazine (TMT) and 4,4'-biphenyldicarbaldehyde (BPDA) th

270 he chelating reagent 2,4,6-trimercapto-1,3,5-triazine (TMT) in the first step and separated by mixed

271 and water, with another equivalent of 1,3,5-triazine to give compounds containing three linked heter

272 d from rigorous structural investigations of triazine to heptazine thermal conversion processes have

273 nhibitors by a fused imidazole ring with the triazine to provide imidazo[1,2-a][1,3,5]triazines.

274 n, including core scaffold modification from triazine to purine, improved the in vitro potency agains

275 ighly debated three-body dissociation of sym-triazine to three hydrogen cyanide molecules.

276 ligand, such as 2,4,6-tri(4-pyridinyl)-1,3,5-triazine (tpt), or a metal-complex cluster, into the hex

277 ently reacted to 2,4,6-tri(2'-pyridyl)-1,3,5-triazine (TPTZ) then measured at 593 nm.

278 I) acceptor with 2,4,6-tris(4-pyridyl)-1,3,5-triazine (TPyT) or 5,10,15,20-Tetra(4-pyridyl)-21H,23H-p

279 amed 2,4,6-tris(2,4,6-tribromophenoxy)-1,3,5-triazine (TTBP-TAZ) is reported for the first time in pl

280 le and efficient one-step synthesis of 1,2,4-triazines under mild conditions from readily accessible

281 One popular precursor building block is the triazine unit (C 3N 3), and most postulated amorphous CN

282 network structures are based on cross-linked triazine units.

283 n of highly substituted pyridines from 1,2,4-triazines via the inverse-electron-demand Diels-Alder re

284 2,4,6-Tris(dimethylamino)-1,3,5-triazine was prepared to complete the series; this is, h

285 If excess 1,3,5-triazine was present the initial S(N)Ar product reacted

286 for the preparation of 6-unsubstituted 1,2,4-triazines was also developed.

287 Reaction of 3-aminopyrrole with seven 1,3,5-triazines was studied in a one-step reaction (in situ fo

288 eries of hybrid analogues of monastrol-1,3,5-triazine were designed and developed via one-pot synthes

289 )-substituted derivatives of benzo[ e][1,2,4]triazine were synthesized from 3-chloro- (1c) and 3-iodo

290 en 2,4,6-trifluoro- or 2,4,6-trichloro-1,3,5-triazine were used--1,3,5-triazines that had leaving gro

291 Pyridyl-substituted 1,3,5-triazines were synthesized in good to excellent yields v

292 RAP reagent contains 2,4,6-tris(2-pyridyl)-s-triazine, which forms a blue-violet complex ion in the p

293 id-mediated cyclodehydration gives the fused triazines, which upon alkali treatment afford the desire

294 solid-state reaction of 2,4,6-triamino-1,3,5-triazine with 2,4,6-trichloro-1,3,5-triazine at 1.0-1.5

295 of the C6 ester of the pyrrolo[2,1- f][1,2,4]triazine with amides afforded compounds with increased p

296 hetic scheme was developed to derivatize the triazine with an electrophile for covalent modification

297 4'-methylphen-2'-yl)-4,6-dimethylamino-1,3,5-triazine with ICl provides species differing in the posi

298 ine, pyridazine, pyrimidine, pyrazine, and s-triazine with N and O atoms are studied both experimenta

299 steps in the IEDDA cascade reaction of 1,3,5-triazines with amino-containing dienophiles has been obt

300 s to pyridyl (or pyridone)-substituted 1,3,5-triazines with high potential in various fields of appli

301 amination of functionalized pyridinyl-1,2,4-triazines with low catalyst/ligand loadings enabling the

302 on the cycloaddition reactivity of the 1,2,3-triazine without altering, and perhaps even enhancing, t