ライフサイエンスコーパス: butadiene

1 iamino-2,3-dicyano-1,4-bis[2-aminophenylthio]butadiene).

2 drosilylation of conjugated dienes including butadiene.

3 ion of terminal alkenes and 2,3-dimethyl-1,3-butadiene.

4 tigated for the conversion of ethanol to 1,3-butadiene.

5 e of a radical trap such as 2,3-dimethyl-1,3-butadiene.

6 tive ultimate carcinogenic metabolite of 1,3-butadiene.

7 , trapped in 80% yield with 2,3-dimethyl-1,3-butadiene.

8 anhydride with 1-(tert-butyldimethylsiloxy)-butadiene.

9 he cycloaddition of oxidopyrylium ylides and butadiene.

10 xposed to a model DNA-damaging chemical, 1,3-butadiene.

11 ical or via cyano radicals reacting with 1,3-butadiene.

12 h classical double bonds of a 2,3-disila-1,3-butadiene.

13 %) with no ene product from 2,3-dimethyl-1,3-butadiene.

14 Dehydrohalogenation gives 2-alkyl-1,3-butadienes.

15 ved with 1-substituted and 1,2-disubstituted butadienes.

16 to afford predominantly (E,E)-1,4-diaryl-1,3-butadienes.

17 ization barriers between some cis- and trans-butadienes.

18 is was developed to generate (E)-1-cyano-1,3-butadiene (1) (10:1 E/Z) via tandem S(N)2 and E2' reacti

19 Diels-Alder cycloaddition of s-trans-1,3-butadiene (1) should yield trans-cyclohexene (7), just a

20 eactions leading to (E)- and (Z)-1-cyano-1,3-butadiene (1) were analyzed by density functional theory

21 radical, benzylallenyl radical, 1-phenyl-1,3-butadiene, 1,2-dihydronaphthalene, and naphthalene), wit

22 Exchange of toluene for anisole, 1,3-butadiene, 1,3-cyclohexadiene, thiophenes, pyrroles, or

23 r the isotopomeric species produced from 1,3-butadiene-1,1,4,4-d(4) dissociation.

24 , further studies were carried out using 1,3-butadiene-1,1,4,4-d(4).

25 adducts of p-methoxycarbonylbenzyl trans-1,3-butadiene-1-carbamate and N,N-dimethylacrylamide have be

26 iamino-2,3-dicyano-1,4-bis[2-aminophenylthio]butadiene (10 microm), also prevented the induction of t

27 sized from (Z,Z)-1,4-bis(tert-butylthio)-1,3-butadiene (2) to evaluate the effects of electron-withdr

28 (Z)-1-cyano-1,3-butadiene (Z-1), 4-cyano-1,2-butadiene (2), and 2-cyano-1,3-butadiene (3).

29 y-tert-butyldimethylsilane, (E)-1-phenyl-1,3-butadiene, 2,3-dihydrofuran, and 2,5-dihydrofuran) probe

30 , 4-cyano-1,2-butadiene (2), and 2-cyano-1,3-butadiene (3).

31 d of a hydrogen atom to 1-butyne (3) and 1,2-butadiene (4) to form the 1-buten-2-yl carbocation and r

32 tituted allenes to dienes, and final nitroso/butadiene [4 + 2] cycloadditions.

33 lead directly to 3 was prepared (1-amino-2,3-butadiene, 4) and was found to be an even more potent in

34 yloxy-3Z,5E-hexadienoyl)- 1-aza-2-ethoxy-1,3-butadiene (40) undergoes cycloaddition to produce as the

35 uch as 1-methoxybutadiene (6g) and alkyl 1,3-butadienes (6a, 6j), the diamination is first-order in d

36 nerated polymer-bound 2-(phenylsulfonyl)-1,3-butadiene (9) in situ which underwent Diels--Alder cyclo

37 iamino-2,3-dicyano-1,4-bis(2-aminophenylthio)butadiene], a mitogen-activated protein kinase kinase in

38 ere prepared, including adducts derived from butadiene, acrolein, crotonaldehyde, and styrene, and ex

39 Reaction of 1 with 2,3-dimethyl-1,3-butadiene afforded the compound [Ar*GaCH(2)C(Me)C(Me)CH(

40 -diazines; and 1,3,4-oxadiazoles), 1-aza-1,3-butadienes, alpha-pyrones, and cyclopropenone ketals.

41 amino-2,3-dicyano-1,4-bis[2-aminophenylthio] butadiene) also prevented the effects of NMDA.

42 omass-generated) syngas, can be converted to butadiene, although there is no large commercial activit

43 lysts for the selective hydrogenation of 1,3-butadiene,, an industrially important reaction.

44 2 equiv of (E,E)-1,4-bis(4-bromophenyl)-1,3-butadiene and 1,4-benzoquinone led to the formation of a

45 ally deuterated counterparts (1,1,4,4-D4-1,3-butadiene and 2,3-D2-1,3-butadiene) at two collision ene

46 e, reacts readily with the conjugated dienes butadiene and 2,3-dimethylbutadiene to afford the corres

47 o-2,3-dicyano-1,4-bis(o-aminophenylmercapto) butadiene and 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyra

48 tudies of the photochemistry of 1-phenyl-1,3-butadiene and 4-phenyl-1-butyne.

49 rosoformaldehyde (CHONO) as dienophiles with butadiene and a series of 1- and 2-substituted dienes.

50 romotes asymmetric hydrohydroxyalkylation of butadiene and affords enantioenriched alpha-methyl homoa

51 ls, and C1-C8 hydrocarbons (particularly 1,3-butadiene and benzene) were determined.

52 a new reaction between 2-nitroperchloro-1,3-butadiene and electron-deficient anilines producing the

53 xample, in the classic Diels-Alder reaction, butadiene and ethylene combine to produce cyclohexene.

54 Isoprene is the 2-methyl analog of 1,3-butadiene and is a possible human carcinogen (IARC Group

55 bserved in both the 1,4 and 2,3 positions of butadiene and maleic acid.

56 ydrazine, starting from 2-nitroperchloro-1,3-butadiene and para-nitro aniline, and generated the pote

57 The butadiene and pentadienyl groups exhibit a polarization

58 Polymers with less polar backbones (butadiene and siloxane) show stronger ion aggregation in

59 reactions of 1-methoxy-4-trimethylsiloxy-1,3-butadiene and the corresponding o-xylylene with acryloni

60 plexes 9 and 10/11 that contain the isomeric butadiene and trimethylenemethane (TMM) C(4) fragments,

61 a(3)Pi(u) state have been conducted with 1,3-butadiene and two partially deuterated counterparts (1,1

62 te the (4 + 2) cycloadditions of allene with butadiene and with benzene.

63 der (DA) reactions of phosphaethene with 1,3-butadiene and with isoprene reveal asynchronous transiti

64 rsion of Fe(CO)(4)-cyclobutenes to Fe(CO)(3)-butadienes and CO is thought to proceed through a mechan

65 .e. freely rotating sigma,pi-acyclic carbo-n-butadienes and flexible sigma-cyclic, pi-acyclic carbo-c

66 hat were obtained from 2,3-disubstituted 1,3-butadienes and naphthoquinone followed by dehydrogenatio

67 cloaddition reactions with 2,3-disubstituted butadienes and ynamides, respectively.

68 converting vinylcyclobutane to cyclohexene, butadiene, and ethylene.

69 the literature, many of which have butenes, butadiene, and furan as reaction intermediates.

70 nants such as benzene, nitrogen dioxide, 1,3-butadiene, and particulate matter.

71 ymer systems considered here comprise ether, butadiene, and siloxane backbones with grafted imidazole

72 and dTTP incorporation was preferred at the butadiene- and styrene-derived adducts.

73 ins acrolein; acrylamide; acrylonitrile; 1,3-butadiene; and ethylene oxide) than combustible cigarett

74 no-2,3-dicyano-1,4-bis(o-aminophenylmercapto)butadiene] and the phosphatidylinositol 3-kinase/Akt inh

75 no-2,3-dicyano-1,4-bis(o-aminophenylmercapto)butadiene] and was abolished by the phosphotidinositol 3

76 However, 1,3-butadienes are also formed in the case of ortho-substitu

77 es, the 1-(2-oxazolidinon-3-yl)-3-siloxy-1,3-butadienes are still very reactive in Diels-Alder reacti

78 Nitro-substituted polyhalogenated butadienes are valuable synthetic precursors for polyfun

79 enes (ethylene, propylene, 1-butene, and 1,3-butadiene) are investigated by experiments and density f

80 The photodissociation dynamics of 1,3-butadiene at 193 nm have been investigated with photofra

81 yl cyanide, 1-octene, and trans-1-phenyl-1,3-butadiene at low temperatures and pressures with passive

82 rts (1,1,4,4-D4-1,3-butadiene and 2,3-D2-1,3-butadiene) at two collision energies of 12.7 and 33.7 kJ

83 o-2,3-dicyano-1,4-bis(o-aminophenylmercapto) butadiene] attenuated MSK1 phosphorylation.

84 rticles (JNPs), made from polystyrene-b-poly(butadiene)-b-poly(methylmethacrylate), PS-PB-PMMA, tribl

85 We describe experiments with poly(1,2-butadiene-b-ethylene oxide) (PB-PEO) diblock copolymers,

86 1,3-Butadiene (BD) is an important industrial and environmen

87 1,3-Butadiene (BD) is an important industrial chemical and a

88 efficiently to 1,3-cyclohexadiene (CHD), 1,3-butadiene (BD), and (C2H4)Pt(PPh3)2 to form P2(CHD)2 (>9

89 Four amphiphilic poly((1,2-butadiene)-block-ethylene oxide) (PB-PEO) diblock copoly

90 were cast directly from solution using poly(butadiene-block-2-(dimethylamino)ethyl methacrylate) (PB

91 amino-2,3-dicyano-1,4-bis[2-amino-phenylthio]butadiene) blocked ERK phosphorylation, and also blocked

92 ft), closure to trialene (bicyclo[1.1.0]-1,3-butadiene), bond-shift isomerization to exchange C-2 and

93 s of DEB are produced metabolically from 1,3-butadiene, but S,S-DEB is the most cytotoxic and genotox

94 of label scrambling between maleic acid and butadiene, butadiene is unlikely to be the primary react

95 tercepted by acyclic, 2-silyloxy-substituted butadienes by highly regioselective (4 + 3) cycloadditio

96 rgic reaction of the ethynyl radical and 1,3-butadiene, C(2)H + H(2)CCHCHCH(2) --> C(6)H(6) + H, unde

97 -bearing radical, silylidyne (SiH), with 1,3-butadiene (C4 H6 ) in the gas phase under single-collisi

98 ,6-dialkylphenyl)-1,4-diaza-2,3-dimethyl-1,3-butadiene) carrying nearly unperturbed nitric oxide radi

99 lododecatriene by selective trimerization of butadiene catalyzed by TiCl(4) and ethylaluminum sesquic

100 The abatement of 9 polychloro-1,3-butadienes (CBDs) in aqueous solution by ozone, UV-C(254

101 s it is typical for zirconocene or hafnocene butadiene complexes.

102 polymers (S = poly(styrene) and B = poly(1,4-butadiene)) comprised of a broad polydispersity B block

103 The reactivities of butadiene, cyclopentadiene, furan, thiophene, pyrrole, a

104 haloethylenes and for 6 halogen-substituted butadienes, cyclopropenes, and a cyclobutene.

105 amino-2,3-dicyano-1,4-bis[2-amino-phenylthio]butadiene), demonstrating that signaling pathways downst

106 A 1,4-diamino-2,3-disila-1,3-butadiene derivative of composition (Me2-cAAC)2(Si2Cl2)

107 ar and atom-efficient synthesis of 2-aza-1,3-butadiene derivatives has been developed via nickel-cata

108 -allylic substrates lead to amido 2-sulfinyl butadiene derivatives in excellent yields, with total ch

109 The Ni-mediated oxidative cyclization of butadienes determines the Z/E selectivity.

110 of selected dilithium derivatives of the 1,3-butadiene dianion including cis-dilithio-1,4-bis(TMS)-2-

111 corporation of a poly(ethylene oxide)-b-poly(butadiene) diblock copolymer, we show that membrane prot

112 A alkylation of nearest-neighbor adenines by butadiene diepoxide (BDO(2)) was determined in the oligo

113 ase eta does not bypass the (R,R)- and (S,S)-butadiene diolepoxide N(2)-guanine-N(2)-guanine intra- s

114 ,1'-binaphtyl (BINAP) or 1,4-diphosphino-1,3-butadiene (dpb).

115 isolated as pure compounds: (E)-1-cyano-1,3-butadiene (E-1), (Z)-1-cyano-1,3-butadiene (Z-1), 4-cyan

116 ctions, somewhat more than 1,3-dialkoxy-1, 3-butadienes (e.g., Danishefsky's diene).

117 onal equilibria of 10 methyl-substituted 1,3-butadienes [(E)- and (Z)-1,3-pentadiene; 2-methyl-1,3-bu

118 s [(E)- and (Z)-1,3-pentadiene; 2-methyl-1,3-butadiene; (E)-2-methyl-1,3-pentadiene; 2,3-dimethyl-1,3

119 E)-2-methyl-1,3-pentadiene; 2,3-dimethyl-1,3-butadiene; (E,E)-, (E,Z)-, and (Z,Z)-2,4-hexadiene; 2,5-

120 n byproducts, formed in the trimerization of butadiene: eleven tricyclic C(12)H(20) and one tetracycl

121 arising from the alkylation of adenine N1 by butadiene epoxide (BDO), followed by deamination to deox

122 DA reactions are earlier than the TSs of the butadiene-ethene cycloaddition.

123 obutane, propylene, 2-methylpropene, and 1,3-butadiene even xenon are coencapsulated with other guest

124 ble to molecular epidemiology studies on 1,3-butadiene-exposed workers.

125 H(3) channel shows that isomerization to 1,2-butadiene followed by dissociation is facile.

126 different feedstock possibilities to produce butadiene, followed by a comprehensive summary of the cu

127 n mice treated with 3, 62.5, or 1250 ppm 1,3-butadiene for 10 days and rats exposed to 3 or 62.5 ppm

128 0 days and rats exposed to 3 or 62.5 ppm 1,3-butadiene for 10 days, or to 1000 ppm 1,3-butadiene for

129 ,3-butadiene for 10 days, or to 1000 ppm 1,3-butadiene for 90 days, using a newly developed immunoaff

130 Tetrafluoroethylene and butadiene form the 2 + 2 cycloadduct under kinetic contr

131 ontrast, Y-DeAlBEA was highly active for 1,3-butadiene formation but exhibited no activity for ethano

132 -C(7)H(11)) ligand (<Zr-C> = 2.56(6) A), the butadiene fragment (<Zr-C> = 2.43(5) A), and the amide n

133 on the aromatic ring are conjugated with the butadiene fragment.

134 An alternative route to produce butadiene from biomass is through direct carbohydrate an

135 n this context, on-purpose production of 1,3-butadiene from biomass-derived feedstock is an interesti

136 FTO process, (ii) the catalytic synthesis of butadiene from ethanol, butanol and butanediols, and (ii

137 a growing worldwide renewed interest in the butadiene-from-ethanol route.

138 taldehyde and exhibited low activity for 1,3-butadiene generation.

139 ethyl ester with 2,3-bis(phenylsulfonyl)-1,3-butadiene gives rise to a 7-oxa-1-azanorbornane cycloadd

140 2-Dimethylphenylsilyl-1,3-butadiene has also been prepared from chloroprene on an

141 but-2-ylmethanols (endo- and exo-9) from 1,3-butadiene has been developed.

142 2-Triethoxysilyl-substituted 1,3-butadiene has been prepared in 30-g quantities from chlo

143 alization of unactivated 1,3-dienes, such as butadiene, has been achieved by employing different comm

144 to exhibit high activity and selectivity for butadiene hydrogenation to butenes under mild conditions

145 nd a TADDOL-derived phosphoric acid promotes butadiene hydrohydroxyalkylation to form enantiomericall

146 out in a 4.4 M solution of 2,3-dimethyl-1,3-butadiene in CH2Cl2.

147 Exposure of alcohols 2a-2j to 2-silyl-butadienes in the presence of ruthenium complexes modifi

148 tic conversion of ethanol and butanediols to butadiene, including thermodynamics and kinetic aspects

149 d; experiments with partially deuterated 1,3-butadiene indicate the formation of the thermodynamicall

150 a strain that acquired higher levels of 1,3-butadiene-induced DNA damage, around the same genes, ult

151 EiJ mice, which acquired relatively less 1,3-butadiene-induced DNA damage, we observed increased tran

152 an industrially available bulk chemical, 1,2-butadiene, into dimethyl adipate, which is a valuable fe

153 3-formyl-4-(2-formylaryl)-1-sulfinyl-(1Z,3E)-butadiene iron tricarbonyl complex also underwent diaste

154 Butadiene is a product of petroleum cracking and is prod

155 1,3-Butadiene is an important industrial chemical used in th

156 yflavones with trans, trans-1,4-diphenyl-1,3-butadiene is described.

157 oselective carboboration of 1,1-bisboryl-1,3-butadiene is developed to generate enantioenriched 3,6'-

158 tive cyclization of one s-cis to one s-trans butadiene is facile and exergonic, leading to the observ

159 The dehydration of crotyl alcohol to 1,3-butadiene is facile and occurs over the mildly Bronsted

160 ment of styrene, ethylene, 1-octene, and 1,3-butadiene is illustrated.

161 1,3-Butadiene is metabolized to several epoxides that form D

162 Together, these data show that 1,3-butadiene is primarily metabolized via the 3-butene-1,2-

163 Butadiene is the simplest polyene and has long served as

164 crambling between maleic acid and butadiene, butadiene is unlikely to be the primary reaction interme

165 two-step procedure for preparing 2-alkyl-1,3-butadienes is described.

166 The same step with two s-cis or s-trans butadienes is either kinetically or thermodynamically un

167 Diels-Alder reaction of N-sulfonyl-1-aza-1,3-butadienes is reported enlisting a series of 19 enol eth

168 c spectroscopy of benzylallene (4-phenyl-1,2-butadiene) is presented along with a detailed analysis o

169 es to purify commodity chemicals such as 1,3-butadiene, isobutene, and 1-butene, but the very similar

170 Approximately 500 Tg of 2-methyl-1,3-butadiene (isoprene) is emitted by deciduous trees each

171 ) Sigmag (+) , a(3) Piu ), with 2-methyl-1,3-butadiene (isoprene; C5 H8 ; X(1) A') accessing the trip

172 , commercially available acyclic 1,3-dienes, butadiene, isoprene, and 2,3-dimethylbutadiene, couple t

173 rbene 3-butenylidene rearranges primarily to butadiene, its perfluoro counterpart is predicted to be

174 valent to a sigma(2), pi-coordination of the butadiene ligand to the element atom as it is typical fo

175 es and alkanolamines are separated on a poly(butadiene)-maleic acid on silica stationary phase using

176 incorporation of a bioadhesive coating, poly(butadiene-maleic anhydride-co-L-DOPA) (PBMAD), to non-bi

177 into species and exposure differences in 1,3-butadiene metabolism.

178 analyses of several adducts derived from 1,3-butadiene metabolites provided new insight into species

179 g N(2)-guanine adducts of stereoisomeric 1,3-butadiene metabolites.

180 norbornene, acrylonitrile, methyl acrylate, butadiene, methyl(vinyl)silanediamine, methyl crotonate,

181 /ethylene, propyne/propylene, and butyne/1,3-butadiene mixtures, with unprecedented dynamic separatio

182 C bond path with each of the pentadienyl and butadiene moieties, contrary to the usually depicted glo

183 (1)H NOEs between the butadiene moiety and the DNA positioned the adduct in th

184 gen lone pair with electron density from the butadiene moiety.

185 arbon-carbon double bond of the 2-methyl-1,3-butadiene molecule.

186 benzene circuit results in a flexible 'carbo-butadiene' molecule that has a conductance 40 times lowe

187 fragments ultimately appear in bimetallated butadiene molecules.

188 ons of ethynyl radicals with substituted 1,3-butadiene molecules.

189 d amino acids (FAAs) 1 skeleton from racemic butadiene monoepoxide as a starting material and its app

190 ase inhibitor, was carried out starting from butadiene monoepoxide through a synthetic sequence invol

191 As demonstrated by the coupling of butadiene, myrcene, and 1,2-dimethylbutadiene to represe

192 Reaction with butadiene occurs via a single ambimodal transition state

193 ansformations that entail the combination of butadiene or isoprene (common feedstock), an enoate (pre

194 transition states (TSs) for the phosphethene-butadiene or isoprene DA reactions are earlier than the

195 hrough reaction of pyridyl radicals with 1,3-butadiene or sequentially with two acetylene molecules,

196 both the direct conversion of ethanol to 1,3-butadiene or the formation of this product by the reacti

197 ratio (OR) = 2.30; 95% CI: 1.44, 3.67], 1,3-butadiene (OR = 2.23; 95% CI: 1.28, 3.88), benzene, and

198 benzene (OR = 3.27; 95% CI: 1.17, 9.14), 1,3-butadiene (OR = 3.15; 95% CI: 1.57, 6.32), and benzene.

199 b-PMOXA, and poly(ethylene oxide)-block-poly(butadiene) (PEO-b-PB)) were reacted with externally adde

200 itoring data, concentrations of benzene, 1,3-butadiene, perchloroethylene, and hexavalent chromium de

201 veral different hydrophobic blocks: poly(1,4-butadiene), poly(-caprolactone), and poly(methyl methacr

202 actide) that relies on self-assembly of poly(butadiene)-poly(lactide) (PB-PLA) diblock copolymers fol

203 which internally crosslinked poly(styrene-co-butadiene) polymer nanoparticles self-assembled to form

204 Large (200 nm) poly(ethylene oxide)-b-poly(butadiene) polymer vesicles fuse into giant (>1 mum) ves

205 nds have been investigated as initiators for butadiene polymerization and ethylene oligomerization.

206 Another probe is based on the diphenyl-1,4-butadiene possessing the boronic acid group in the 4' po

207 iamino-2,3-dicyano-1,4-bis[2-aminophenylthio]butadiene), prevented BDNF's suppressive effects on coca

208 propargyl epoxides leads to 1,2-diborylated butadienes probably via en allenylboronate intermediate.

209 ]octa-2,5-diene, and benzobarrelene with 1,3-butadienes proceed in excellent yields using cobalt-base

210 the (E) and (Z) isomers of the resulting 1,3-butadiene radical cations depends largely on steric effe

211 re much lower than that of the parent ethene-butadiene reaction, 28 kcal/mol, even though the exother

212 les (C(2)) with C(4)H(6) isomers such as 1,3-butadiene represent a potential, but hitherto unnoticed,

213 zed hydrogen transfer from 4-aminobutanol to butadiene results in the pairwise generation of 3,4-dihy

214 ion, the main constituents of tires, styrene butadiene rubber (SBR) and polyisoprene (IR), has been i

215 2) cofeed impact on the pyrolysis of styrene butadiene rubber (SBR) was investigated using thermograv

216 d by black foams (66%, identified as styrene-butadiene rubber) and to a lesser extent fibers/lines (2

217 eused scrap tires (main constituent, styrene butadiene rubber, SBR), which might be harmful to the en

218 ere employed during 1943-1984 in two styrene-butadiene rubber-manufacturing plants in the United Stat

219 s the most accurate way of modelling styrene-butadiene rubber-silica composite formation.

220 ith cyclohexa-1,3-diene and 2,3-dimethyl-1,3-butadiene (several cycloadducts characterized by X-ray c

221 iamino-2,3-dicyano-1,4-bis(2-aminophynylthio)butadiene]-specific inhibitors of mitogen-activated prot

222 Butadiene, specifically, would be a useful substrate bec

223 ice was printed in transparent acrylonitrile butadiene styrene (ABS) and contained a 400 mum wide str

224 ely 180 mug/min), styrene from acrylonitrile butadiene styrene (ABS) and high-impact polystyrene (HIP

225 ed for in situ analysis during acrylonitrile butadiene styrene (ABS) and polylactic acid (PLA) 3D pri

226 Acrylonitrile butadiene styrene (ABS) filaments generated the largest

227 structure made from commercial Acrylonitrile Butadiene Styrene (ABS) modules, known as LEGO(R) blocks

228 Acrylonitrile butadiene styrene (ABS), extruded at a higher temperatur

229 microparticles in the polymer acrylonitrile butadiene styrene (ABS), which may be used with a commer

230 printed fittings prepared from acrylonitrile butadiene styrene (ABS).

231 nd sludge, and polystyrene and acrylonitrile butadiene styrene were the most common polymers quantifi

232 electrode were fabricated from acrylonitrile-butadiene-styrene (ABS) and conductive graphene polylact

233 vapor bath was used to smooth acrylonitrile-butadiene-styrene (ABS) surfaces and facilitate bonding

234 of carbon nanotubes (CNTs) and acrylonitrile-butadiene-styrene (ABS) was analyzed with respect to its

235 manufacturing processes using acrylonitrile-butadiene-styrene polymer feedstock.

236 eposition modeling (FDM) using acrylonitrile-butadiene-styrene.

237 tegy using a boron/tin hetero-bis-metallated butadiene system.

238 n atoms are attached to C2 and C3 of the 1,3-butadiene tether.

239 entafluorophenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene; TFA = trifluoroacetate] has been reported to

240 entafluorophenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene; TFA is trifluoroacetate] converts benzene, et

241 n to one of the terminal carbon atoms of 1,3-butadiene, the collision complex undergoes trans-cis iso

242 on VPO catalysts to produce maleic acid and butadiene, the isotopic labels were observed in both the

243 on, which undergoes thermal rearrangement to butadiene, the perfluoro compound will yield hexafluoroc

244 For butadiene, the ratio of label scrambling was consistentl

245 the reaction of 1,1-difluoroallene with 1,3-butadiene, the results of which indicate that the use of

246 For trans-1-phenyl-1,3-butadiene, the stable alkyl complex is an eta(3)-allyl c

247 with thiophene to give eta(5)-thiophene and butadiene-thiolate complexes, (eta(5)-C(4)H(4)S)Mo(PMe(3

248 To specifically examine metabolism of 1,3-butadiene to 1,2;3,4-diepoxybutane, the formation of the

249 4-addition across the commodity chemical 1,3-butadiene to afford skipped polyene products is reported

250 ination of H2C horizontal lineNH and cis-1,3-butadiene to form a six-membered ring was examined by qu

251 oceed efficiently from 1 to 2,3-dimethyl-1,3-butadiene to form Diels-Alder product 3 with a zero-orde

252 gered carbon-carbon coupling of alcohols and butadiene to form products of carbonyl crotylation with

253 ar [2pi + 2pi] cycloaddition of ethylene and butadiene to form vinylcyclobutane.

254 dy also extends Singleton's investigation on butadiene to regioselectivity.

255 ed dienes are copolymerized efficiently with butadiene to stereoregular copolymers by [(mesitylene)Ni

256 of 1,4-, 1,3-, and 2,3-bis(2-nitroaryl)-1,3-butadienes to afford 2,2'-, 2,3'-, and 3,3'-biindoles, r

257 s of many plants emit isoprene (2-methyl-1,3-butadiene) to the atmosphere, a process which has import

258 fting materials [such as 1,1,4,4 Tetraphenyl Butadiene (TPB)] have several disadvantages and are unre

259 The compounds are a butadiene (U-0126), an N-alkoxy amide (CI-1040), two CI-

260 , 1,4-diamino-2,3-dicyano-1,4-bis(methylthio)butadiene (U0126) and 2'-amino-3'-methoxyflavone (PD9805

261 o-2,3-dicyano-1,4-bis(o-aminophenylmercapto) butadiene (U0126) before fear conditioning.

262 eatment with 1,4-diamino-2,3-dicyano-1,4-bis butadiene (U0126) could significantly inhibit mouse brai

263 y 1,4-diamino-2,3-dicyano-1,4-bis(methylthio)butadiene (U0126) of an HGF downstream kinase mitogen-ac

264 diamino-2,3-dicyano-1,4-bis(2-aminophynyltio)butadiene (U0126), and ER antagonist ICI-182780 failed t

265 amino-2,3-dicyano-1,4-bis(2-aminophenylthio) butadiene (U0126), and tyrphostin AG1478.

266 amino-2,3-dicyano-1,4-bis(2-aminophenylthio)-butadiene (U0126), attenuated insulin action, indicating

267 diamino-2,3-dicyano-1,4-bis(2-aminophynyltio)butadiene (U0126), or Rho kinase signaling with R-(+)-tr

268 r 1,4-diamino-2,3-dicyano-1,4-bis(methylthio)butadiene (U0126), two ERK kinase MAP inhibitors, wherea

269 y 1,4-diamino-2,3-dicyano-1,4-bis(methylthio)butadiene (U0126), which blocks the phosphorylation of E

270 1,4-diamino-2,3-dicyano-1,4-bis(methylthio) butadiene (U0126)], and therefore cAMP-dependent target

271 [1,4-diamino-2,3-dicyano-1,4-bis(methylthio)butadiene (U0126)], whereas PAR2 effects were only block

272 mprises initial isomerizations of allenes to butadienes under N2 and subsequent oxidations of N-hydro

273 no-2, 3-dicyano-1, 4-bis (2-aminophenylthio) butadiene (UO126; for ERK1/2), trans-1-(4-hydroxyclycloh

274 benzenes were prepared from 2,3-dimethyl-1,3-butadiene using Diels-Alder cycloadditions and Pd(0)-cat

275 nacyclopentadienes were readily converted to butadienes via reactions with acids.

276 ydes and ketones, furans, acrylonitrile, 1,3-butadiene, vinyl chloride, and nitromethane) in the micr

277 es RCH=CH(2) (R = SiMe(3), CH(3)CH(2)CH(2)), butadiene, vinylarenes ArCH=CH(2) (Ar = phenyl, 4-methyl

278 enteen SBS triblock copolymers with poly(1,4-butadiene) volume fractions 0.27 </= f(B) </= 0.82, we d

279 Additionally, 1,3-dipyrrolidino-1,3-butadiene was shown to be significantly more reactive th

280 Acrolein, furan, acrylonitrile, and 1,3-butadiene were considered to be the most harmful VOCs.

281 reactions of substituted cyclopropenes with butadiene were explored with M06-2X density functional t

282 e syntheses of several 2,3-disubstituted 1,3-butadienes were achieved.

283 oup nonbonded interactions in conjugated 1,3-butadienes were delineated.

284 Arylated butadienes were prepared employing transition-metal coup

285 chiral 1-(2-oxazolidinon-3-yl)-3-siloxy-1,3-butadienes were prepared from readily available starting

286 similar in mice exposed to 3 or 62.5 ppm 1,3-butadiene, whereas 2-hydroxy-3-butenyl-valine was 3-fold

287 )(-), each with two pi bonds, are similar to butadiene, while H(2)B(10)(2-), H(2)B(11)(-), and H(2)B(

288 ctive, while 1-methoxy-4-trimethylsiloxy-1,3-butadiene will give a small preference ( approximately 5

289 solution in the presence of 2,3-dimethyl-1,3-butadiene with a quantum efficiency of approximately 38%

290 For the reaction of 2,3-dimethyl-1,3-butadiene with acrylonitrile, the concerted reaction is

291 tensive efforts to cooligomerize isoprene or butadiene with alkynes in a controlled fashion by zerova

292 cycloaddition of 2,3-bis(phenylsulfonyl)-1,3-butadiene with an appropriate oxime.

293 tepwise reactions of tetrafluoroethylene and butadiene with density functional theory, DFT (B3LYP and

294 rearrangement to the Diels-Alder reaction of butadiene with ethylene is discussed.

295 ding the parent Diels-Alder cycloaddition of butadiene with ethylene, electrocyclic ring-opening of c

296 solid catalyst for the polymerization of 1,3-butadiene with high stereoselectivity (>99% 1,4-cis).

297 the treatment of a 1-aminoethyl-substituted butadiene with maleic anhydride at 0 degrees C to room t

298 volatile hydrocarbon isoprene (2-methyl-1,3-butadiene), with subsequent analysis of isoprene by head

299 cylaniline and the volatile 2,3-dimethyl-1,3-butadiene, with an outlier being operationally defined a

300 1-cyano-1,3-butadiene (E-1), (Z)-1-cyano-1,3-butadiene (Z-1), 4-cyano-1,2-butadiene (2), and 2-cyano-