ライフサイエンスコーパス: butane

1 ring strain associated with azabicyclo[1.1.0]butane.

2 and 2,2',4,4'-tetra-tert-butylbicyclo[1.1.0]butane.

3 xidation of hydrocarbons such as methane and butane.

4 d mainly from the two methylene carbons of n-butane.

5 e with hydrocarbons such as ethylbenzene and butane.

6 ster than that of the simple model, azo-tert-butane.

7 harge of +/-1e to a terminal methyl group of butane.

8 -(maleimidomethyl)-cyclohexane-ca rboxamido ]butane.

9 nd incorporation of the additive 1,4-diamino butane.

10 o the strained C-C bond of the bicyclo[1.1.0]butane.

11 teresis in ethane, propane, n-butane and iso-butane.

12 ced hysteresis was found in n-butane and iso-butane.

13 ain alkanes, principally ethane, propane and butane.

14 cracking and dehydrogenation reactions of n-butane.

15 onoxidizing radical initiation with azo-tert-butane.

16 heteroarenes with alkenes and bicyclo[1.1.0]butanes.

17 e single-electron oxidation of bicyclo[1.1.0]butanes.

18 functionalized, stereoenriched bicyclo[1.1.0]butanes.

19 of two compounds, 4-(4-phenoxyphenylsulfonyl)butane-1,2-dithiol (compound 1) and 5-(4-phenoxyphenylsu

20 anedioic acid (PMPA) and 4,4'-phosphinicobis(butane-1,3-dicarboxylic acid) (PBDA) were built by a com

21 boxypeptidase inhibitor 4,4'-phosphonicobis (butane-1,3-dicarboxylic acid) can inhibit this activity.

22 r MDL 72527 (N(1),N(4)-Di(buta-2,3-dien-1-yl)butane-1,4-diamine dihydrochloride), an inhibitor of SMO

23 (methylene))tris(N(4)-(4-(methylamino)b utyl)butane-1,4-diamine, 6b, which contained three N-methylho

24 the inner phase of a hemicarcerand with four butane-1,4-dioxy linker groups (5) in C(6)D(5)CD(3) at 7

25 a hemicarcerand with deuterated spanners and butane-1,4-dioxy linker groups (d(48)-5).

26 ed diamino diethers including (2S,2'S)-1,1'-(butane-1,4-diylbis(oxy))bis(N-isopropylpropan-2-amine) 7

27 than for the formation of the bicyclo[1.1.0]butanes 11.

28 conditions, 2b with PhLi gave bicyclo[1.1.0]butane 11b accompanied by bromophenyl derivative 8b.

29 went a smooth rearrangement to bicyclo[1.1.0]butane 11b at -78, -10, or +35 degrees C.

30 by volume (ppbv)], propane (20 ppbv), and n-butane (13 ppbv) were observed in north-central Texas.

31 -ribityl-1,3,7-trihydropurine-2,6,8-trionyl)]butane (18), was also synthesized using a similar route

32 -(2R,3R)-2-carbomethoxy-3-cyano-2,3-diphenyl-butane 2 with two adjacent stereogenic, all-carbon subst

33 ive nickel catalyst for the dry reforming of butane, 2) an agile magnetic-controlled particle, and 3)

34 oted Ferrier carbocyclization and persistent butane-2,3-diacetal protection to produce a key chiral c

35 ultaneous determination of propane-1,2-diol, butane-2,3-diol, and propane-1,3-diol in cheese and bact

36 The detection limits for propane-1,2-diol, butane-2,3-diol, and propane-1,3-diol in cheese samples

37 reaction between urea and diacetylmonoxime (butane-2,3-dionammonoxime).

38 arginine-specific reagents phenylglyoxal and butane-2,3-dione irreversibly inactivate the Tritrichomo

39 l background, the reactivity of Arg-144 with butane-2,3-dione is low ( approximately 25%) and is redu

40 was monitored with the Arg-specific reagent butane-2,3-dione using electrospray ionization mass spec

41 nonanal, ethyl acetate, ethyl octanoate, and butane-2,3-dione) representative of the four chemical cl

42 rg187), was susceptible to phenylglyoxal and butane-2,3-dione.

43 ong aromatic aldehydes, aromatic amines, and butane-2,3-dione.

44 emonstrated on stereoisomeric forms of 4,4'-(butane-2,3-diyl)bis(piperazine-2,6-dione).

45 ted 1,3-dibora-2,4-diphosphoniobicyclo[1.1.0]butane (3) under mild conditions, substantiating some fo

46 cm(-1)), CH(4)), isopentane (765 cm(-1)), i-butane (798 cm(-1)), n-butane (830 cm(-1)), n-pentane (8

47 1,2,3,4-tetrakis(4,6-dimethyl-s-triazin-2-yl)butane (8).

48 ntane (765 cm(-1)), i-butane (798 cm(-1)), n-butane (830 cm(-1)), n-pentane (840 cm(-1)), propane (86

49 oraphane [1-isothiocyanato-4-(methylsulfinyl)butane], a naturally occurring isothiocyanate derived fr

50 bench-stable benzoylated 1-azabicyclo[1.1.0]butane (ABB) can be harnessed for nickel-catalyzed Suzuk

51 inherent ring strain of the azabicyclo[1.1.0]butane (ABB) fragment.

52 ed from the highly strained azabicyclo[1.1.0]butane (ABB), can undergo divergent strain-release react

53 rmation, analogous to the recently described butane activation by 'Candidatus Syntrophoarchaeum'(9).

54 rmation, analogous to the recently described butane activation by 'Candidatus Syntrophoarchaeum'(9).

55 1-Substituted bicyclo[1.1.0]butanes add enantioselectively to 2(1H)-quinolones upon

56 e-energy differences obtained from CO2 and n-butane adsorption isotherms.

57 The presence of ethane, propane, and n-butane, along with the methane isotopic composition, ind

58 e [(-)-1-isothiocyanato-(4R)-(methylsulfinyl)butane], an isothiocyanate abundant as its glucosinolate

59 From aminodiborane, an inorganic butane analogue, NH(3)BH(2)NH(2)BH(3), was prepared, and

60 stitution in 2,2'-di-tert-butylbicyclo[1.1.0]butane and 2,2',4,4'-tetra-tert-butylbicyclo[1.1.0]butan

61 bstitution in 1,3-di-tert-butylbicyclo[1.1.0]butane and 2,2',4,4'-tetramethyl-1,3-di-tert-butylbicycl

62 rans-epoxysuccinyl-l-leucylamido(4-guanidino)butane and a novel substrate mimetic peptide inhibitor.

63 ell (SOFC) cermet anodes operating with both butane and CO fuel feeds.

64 y shows a preliminary monitoring of propane, butane and dimethyl ether residues, in cakes and chocola

65 Release kinetics of propane, butane and dimethyl ether were measured over one day wit

66 Degenerate ring inversion in bicyclo[1.1.0]butane and eight of its fluorinated derivatives has been

67 butane, and ethane, the time constants for n-butane and ethane internal rotation under the same condi

68 '-tetramethyl-1,3-di-tert-butylbicyclo[1.1.0]butane and geminal substitution in 2,2'-di-tert-butylbic

69 a strain-release diboration of bicyclo[1.1.0]butane and intramolecular deborylative alkylation.

70 ion isotherms of methane, ethane, propane, n-butane and iso-butane as well as carbon dioxide for two

71 rature, the sorption isotherms of propane, n-butane and iso-butane were measured to 8, 2, and 2 bar,

72 adsorption hysteresis in ethane, propane, n-butane and iso-butane.

73 he most pronounced hysteresis was found in n-butane and iso-butane.

74 le than their normal isomers, for example, n-butane and n-pentane.

75 rans-epoxysuccinyl-l-leucylamido(4-guanidino)butane and our new peptide inhibitor and the effects of

76 Powered by the combustion of butane and oxygen, this robot is able to perform untethe

77 an methane by mole at 2 bar, followed by iso-butane and propane.

78 able dehydrogenation activation barrier of n-butane and reasonable desorption barrier of butene in th

79 s hydrocarbons (methane, ethane, 1-butene, n-butane and toluene) using a solid-oxide fuel cell at 973

80 igma + 2pai] cycloaddition of bicyclo[1.1.0]-butanes and 1,3-dienes.

81 d bicyclo[3.1.1]heptanes using bicyclo[1.1.0]butanes and cyclopropylamines.

82 Sulfone-substituted bicyclo[1.1.0]butanes and housanes have found widespread application i

83 ulations of sterically crowded bicyclo[1.1.0]butanes and their radical cations.

84 ane, ethane, ethylene, propane, propylene, n-butane, and 1-butene in ZIF-8 are reported over a temper

85 hydrocarbons bromocyclo-propane, bromocyclo-butane, and bromocyclo-pentane upon Br(3d) and C(1s) inn

86 calculations of the barrier heights of 1, n-butane, and ethane, the time constants for n-butane and

87 other gaseous alkanes/alkenes (e.g., ethane, butane, and ethene) to select and fuel indigenous microo

88 erformance for separation of n-butane from i-butane, and for other technologically important hydrocar

89 The adsorptions of propane, n-butane, and iso-butane were much higher than methane at

90 onal hydrocarbon products [alpha-butylene, n-butane, and methane (CH(4))] in a scaled-up reaction fea

91 that C(2+) n-alkane gases (ethane, propane, butane, and pentane) are initially produced by irreversi

92 nerates sigma-ethane, sigma-propane, sigma-n-butane, and sigma-i-butane complexes.

93 nd abstraction of the two methyl groups of n-butane, and the two methylene groups of n-butane form et

94 on the Ni cermet anode following exposure to butane, and under open circuit voltage (OCV) conditions

95 1-propanol and propionaldehyde were added to butane- and ethane-grown cells, indicating that propiona

96 butylated h-SWNTs showed that 1-butene and n-butane are formed during thermolysis.

97 The resulting bicyclo[1.1.0]butanes are converted with high regioselectivity to unpr

98 ylpyridine, dppb = 1,4-bis(diphenylphosphino)butane) are highly active for the transfer hydrogenation

99 other short-chain alkanes such as ethane and butane as carbon and energy sources, thus expanding the

100 f methane, ethane, propane, n-butane and iso-butane as well as carbon dioxide for two shales and isol

101 of saturated hydrocarbons, e.g., propane and butane as well as oxygen-atom transfer (OAT) to unsatura

102 Using bicyclo[1.1.0]butanes as cation precursors, the regio- and stereochemi

103 With bicyclo[1.1.0]butanes as coupling partners, this dearomative [2pai + 2

104 to quantify the formation of 1-butene from n-butane, as well as the formation of a distribution of sh

105 ies show that the formation of graphite with butane at OCV leads first to decreased cell performance

106 a-VOPO4 to delta-VOPO4 occurs on exposure to butane at the reaction temperature, and hence the metast

107 Bicyclo[1.1.0]butane (BCB) has predominantly been explored as an elect

108 on with another strained unit, bicyclo[1.1.0]butane (BCB), enables the reactivity of both pai-units i

109 Cycloadditions using bicyclo[1.1.0]butanes (BCB) offer a promising solution along those lin

110 /reverse mode of reactivity in bicyclo[1.1.0]butanes (BCB).

111 Bicyclo[1.1.0]butanes (BCBs) are valuable substrates in the "strain re

112 the synthesis of sulfoximine bicyclo[1.1.0] butanes (BCBs) as novel thiol reactive chiral warheads,

113 eactivity of cyclopropanes and bicyclo[1.1.0]butanes (BCBs) has been extensively studied, higher homo

114 sis, ring-opening reactions of bicyclo[1.1.0]butanes (BCBs) provide an attractive pathway to construc

115 for the difunctionalization of bicyclo[1.1.0]butanes (BCBs) under high regio- and syn-selectivity is

116 however, their synthesis from bicyclo[1.1.0]butanes (BCBs) via direct metal carbene insertion remain

117 Bicyclo[1.1.0]butanes (BCBs), strained carbocycles comprising two fuse

118 F(5) radical, which engages azabicyclo[1.1.0]butanes bearing ketone, ester, alkyl, or aryl substituen

119 -[4'-(maleimidomethyl)cyclohexanecarboxamido]butane (BMCC).

120 (4'-[maleimidoethyl-cyclohexane]-carboxamido)butane (BMCC).

121 ne)bisphenol (BPAP), 2,2-bis(4-hydroxyphenyl)butane (BPB), 4,4'-dihydroxydiphenylmethane (BPF), 4,4'-

122 ans-epoxysuccinyl-l-leucylamido-(4-guanidino)butane but not by NH(4)Cl, which raises the endocytic pH

123 (x) allows continuous control of n-butane, i-butane, butanol, and isobutanol diffusivities over 2-3 o

124 bene (:CF(2)) to electron-rich bicyclo[1.1.0]butanes by the CF(3)TMS/NaI system.

125 intermediate addition into the bicyclo[1.1.0]butane C-C bond.

126 xchanged clusters show that propane (C3) and butane (C4) dithiols have ideal chain lengths for inters

127 is demonstrated for the gaseous constituents butane, carbon dioxide, cyclopropane, isobutylene, and m

128 Hydrogenolysis of n-butane catalyzed by these hydrides was carried out at lo

129 al constraint in the otherwise freely mobile butane chain.

130 mical looping-oxidative dehydrogenation of n-butane (CL-ODHB).

131 tment using four different gases, propane, n-butane, CO(2) and liquefied petroleum gas (LPG), was inv

132 , sigma-propane, sigma-n-butane, and sigma-i-butane complexes.

133 f methane flow rates; ethane, propane, and n-butane concentrations; isotopes of methane; and noble ga

134 Bicyclo[1.1.0]butane-containing compounds feature a unique chemical re

135 strained hydrocarbons, such as bicyclo[1.1.0]butane, continues to expand, it becomes increasingly adv

136 to CL-ODH of other light alkanes such as iso-butane conversion to iso-butylene, providing a generaliz

137 However, an oligodeoxyribonucleotide with a butane cross-link was a very poor substrate for AGT-medi

138 This reaction is greatly hindered with the butane cross-link, which is mostly buried in the active

139 se ligand, namely, 1,4-bis(diphenylphosphino)butane (DBPP), for the synthesis of CsPbBr(3) NCs.

140 ecially the sub-nano structure) effects on n-butane DDH reaction at the atomic level.

141 s an outstanding catalytic performance for n-butane dehydrogenation, with a remarkable n-butane react

142 served that isobutene inhibits the rate of n-butane dehydrogenation.

143 able model ICL, 1,3-bis(2'-deoxyguanos-N2-yl)butane derivative, was also employed to probe the ICL re

144 ells, when grown in citrate and incubated in butane, developed butane oxidation capability and accumu

145 tion of PAO by N,N'-bis(2, 3-butadienyl)-1,4-butane-diamine results in a significant reduction of the

146 racking and dehydrogenation of propane and n-butane differed among zeolites with varying channel stru

147 oride; 2) 8 mmol/L egtazic acid; 3) 5 mmol/L butane-dione-monoxime (BDM); or 4) 50 mmol/L ammonium ch

148 3) Butane-dione-monoxime and NH4Cl chloride affected contra

149 remarkable alkene selectivity (99.0%) for n-butane direct DDH reaction at 450 C, compared to typical

150 dispersed Sn promoters, and correlated the n-butane direct dehydrogenation (DDH) activity with the av

151 ct, 2,3-dimethyl-2,3-(5,10-thianthreniumdiyl)butane ditetrafluoroborate (12), was isolated at -15 deg

152 yzed by Pd2(dba)3, 1,4-bis(diphenylphisphino)butane (dppb), and syngas (CO/H2) in chloroform/alcohol.

153 ans-epoxysuccinyl-L-leucylamide-(4-guanidino)butane (E-64) against western corn rootworm gut proteina

154 rans-epoxysuccinyl-L-leucylamino(4-guanidino)butane (E-64) inhibited invasion by 75%.

155 transepoxy-succinyl-leucylamido-(4-guanidino)butane (E64) causes an accumulation of an intermediate n

156 transepoxy-succinyl-leucylamido-(4-guanidino)butane (E64).

157 -2,3-epoxypropionyl-leu-amido-(4-guanidinio )butane ethyl ester (E64d) and carbenzoxy-leu-leu-tyr-CHN

158 ctivity in an open-path configuration, and a butane flame served as the OH source during testing.

159 ss involves sensitization of a bicyclo[1.1.0]butane followed by cycloaddition with an alkene.

160 he barrels by the pyrolytic decomposition of butane, followed by electrodeposition of a thin layer of

161 ne dicarboxylic acid for PEN) and ethane (or butane for PBT) in essentially quantitative yield.

162 n-butane, and the two methylene groups of n-butane form ethylene.

163 nsation reaction of 1,4-bis(organylphosphino)butane, formaldehyde, and primary amines.

164 n laser-initiated oxidation experiments of n-butane, formic acid and acetone are produced on the time

165 In the limit of a large oxide flux, excess butane forms ordered graphite but only transiently.

166 prototypical chiral molecule 1-iodo-2-methyl-butane ([Formula: see text] [Formula: see text]I) in a p

167 ans-epoxysuccinyl-L-leucylamido-(4-guanidino)butane (FP2E-64) formed a complex with hemoglobin, but D

168 NiEt(2) (3) results in elimination of cod or butane from 2 and 3, respectively, and oxidative additio

169 xhibits high performance for separation of n-butane from i-butane, and for other technologically impo

170 Conversion of propane or butanes from natural/shale gas into propene or butenes,

171 r emissions of methane, ethane, propane, and butanes from oil and gas sources in the Barnett Shale pr

172 for the synthesis of 1-sulfonylbicyclo[1.1.0]butanes from readily available methyl sulfones and inexp

173 d mixture of methane, ethane, propane, and n-butane gases in pure water and aqueous electrolyte syste

174 detection, using monodeuterated propane and butane generated in situ as internal standards.

175 -trans-epoxysuccinyl-leucylamide-(4-guanido)-butane] greatly reduces induction of BVEC apoptosis.

176 ., d(13)C ethane > d(13)C propane > d(13)C n-butane > d(13)C n-pentane).

177 Oxidative dehydrogenation (ODH) of n-butane has the potential to efficiently produce butadien

178 tion of N-heterocyclic phosphine-butane (NHP-butane) has been developed.

179 Bicyclo[1.1.0]butanes have attracted significant attention from synthe

180 iated with each cluster compound (Au:SR, R = butane, hexane, dodecane).

181 parameter (x) allows continuous control of n-butane, i-butane, butanol, and isobutanol diffusivities

182 performance for both propylene/propane and n-butane/i-butane separation, displaying permeability and

183 such as meso-2,3-bis(2,6-dioxopiperazin-4-yl)butane (ICRF-193), are widely believed to be only cataly

184 topically labeled ethylene as did [1,4-(13)C]butane, indicating that ethylene was produced mainly fro

185 action in which (13)C-isotopically labeled n-butane is flowed over a catalyst bed and the reaction pr

186 lar cyclopropanation to form a bicyclo[1.1.0]butane is followed by a photoinduced formation of a trip

187 cloaddition of aziridines with bicyclo[1.1.0]butanes is described.

188 Gases such as propane, butane, isobutane, propylene, 2-methylpropene, and 1,3-b

189 filtration of these suspensions exhibit an n-butane/isobutane selectivity of 5.4, with an n-butane pe

190 GPU) and a high selectivity over n-butene, n-butane, isobutene, and isobutane (9.72, 9.94, 10.31, and

191 hibit record high permeances for xylene- and butane-isomers.

192 rans-epoxysuccinyl-l-leucylamido-4-guanidino butane, leupeptin, pepstatin-A, chloroquine, and NH(4)Cl

193 The synthesis of butane-like (GeH(3))(2)(SiH(2))(2) (1), (GeH(3))(2)SiH(S

194 We report the synthesis of new bicyclo[1.1.0]butane-linked heterocycles by a nucleophilic addition of

195 n kinetics as exemplified in this work for n-butane/methane, butanol/methanol, and butanol/water pair

196 We report here the formation of perfluoro-n-butane microbubbles coated with surface-active proteins

197 D moiety a diethylphosphate linked through a butane moiety.

198 ts of zeolite structure on the kinetics of n-butane monomolecular cracking and dehydrogenation are in

199 Butane monooxygenase (BMO) from Pseudomonas butanovora h

200 that 1,2-cis-DCE epoxide was a substrate for butane monooxygenase (BMO) that was oxidized after the p

201 ra to consume C2 to C8 alkane substrates via butane monooxygenase (BMO) were examined.

202 s an alcohol-inducible alkane monooxygenase, butane monooxygenase (BMO), that initiates growth on C(2

203 itutions in the hydroxylase alpha subunit of butane monooxygenase (BMOH-alpha) in P. butanovora.

204 o acid substitutions in the alpha-subunit of butane monooxygenase hydroxylase (BMOH-alpha) were compa

205 the utilization of N-heterocyclic phosphine-butane (NHP-butane) has been developed.

206 n C from day 0 to day 6 of storage (3-methyl butane nitrile) and temperature (limonene) are identifie

207 ongly suggests that the total oxidation of n-butane on VPO catalysts involves the oxidation and abstr

208 Pseudomonas butanovora grown on butane or 1-butanol expresses two 1-butanol dehydrogenas

209 oh and bdh inactivated was unable to grow on butane or 1-butanol.

210 polyester resins, is made by oxidation of n-butane over vanadium phosphate catalysts.

211 n citrate and incubated in butane, developed butane oxidation capability and accumulated 1-butanol.

212 acid+acetone products from observations of n-butane oxidation in two complementary experiments.

213 was always observed as a side product for n-butane oxidation on VPO catalysts.

214 rotein) and BDH (a quinohemoprotein), in the butane oxidation pathway of P. butanovora.

215 f 12 catalysts toward ethane, propane, and n-butane oxidation reactions.

216 unctional theory to study the mechanism of n-butane oxidation to maleic anhydride on the vanadium pho

217 nd corresponded with a lower maximum rate of butane oxidation.

218 ive to many of the reactants and products of butane oxidation.

219 e enzymes that are similar to those found in butane-oxidizing archaea, as well as several enzymes pot

220 syntrophic methane-, ethane-, propane-, and butane-oxidizing marine archaea with sulfate-reducing ba

221 ,2,3-triphospha-4-azatricyclo [1.1.0.0(2,4)] butane (P(3)N) molecule-an isovalent species of phosphor

222 ed assembly is observed with methane through butane, pentane triggers assembly, and hexane through oc

223 Conformational free energies of butane, pentane, and hexane in water are calculated from

224 tane/isobutane selectivity of 5.4, with an n-butane permeance of 3.5x10(-7) mol m(-2) s(-1) Pa(-1) (c

225 Liquefied butane pressurized under nitrogen and doped with arsine

226 Fully (13)C-labeled butane produced about 5-13 times as much isotopically la

227 ppb (1,4-bis(di(pentafluorophenyl)phosphino)butane) promotes highly branch-selective hydroarylation

228 talyzed cycloisomerizations of bicyclo[1.1.0]butanes provide a fruitful approach to cyclopropane-fuse

229 es, and thiazoles with alkenes/bicyclo[1.1.0]butanes, providing access to unprecedented C(sp(3))-rich

230 Sterically crowded bicyclo[1.1.0]butane radical cations are therefore promising candidate

231 When [1,4-(13)C]n-butane reacted on VPO catalysts to produce maleic acid a

232 -butane dehydrogenation, with a remarkable n-butane reaction rate (8.8 mol.g(Ir)(-1).h(-1)) and high

233 in organic chemistry, the elucidation of the butane rotation barriers is fundamental for structural t

234 The central butane segment of BE-4-4-4 was replaced with a 1,2-subst

235 nce of conformational mobility at the 4N, 9N-butane segment of BES for its biological activity.

236 1N,12N-Bisethylspermyne, where the central butane segment of BES was replaced by the rigid 2-butyne

237 By replacing the central butane segment of BES with a 1,2-disubstituted cycloprop

238 xicity was markedly reduced when the central butane segment was deprived of its rotational freedom by

239 When the butane segment was replaced by a benzene-1,2-dimethyl re

240 logous pair of isomers was obtained when the butane segment was replaced with a 1, 2-disubstituted cy

241 turation(s) was also introduced at the outer butane segment(s) of BE-4-4-4.

242 ce for both propylene/propane and n-butane/i-butane separation, displaying permeability and ideal sel

243 s (SCGAs, consisting of ethane, propane, and butane) serves as an efficient sink to mitigate these ga

244 bound either to the cyclohexene ring or the butane side chain.

245 This is the first report of propane and butane sorption isotherms in shales.

246 his study, the PFAS alternative, perfluoro-1-butane-sulfonamide (FBSA), was identified for the first

247 bile phase of acetic acid, acetonitrile, and butane-sulfonic acid.

248 th ethyl iodide, 1,3-propane sultone, or 1,4-butane sultone) to give water-soluble imidazolium- porph

249 -Crafts spirocyclization of azabicyclo[1.1.0]butane-tethered (hetero)aryls for the synthesis of a uni

250 pellane, [3.1.1]propellane and bicyclo[1.1.0]butanes that proceeds under practical, scalable and mild

251 When induced with butane, the gene for BOH was expressed earlier than the

252 (infinity), bbtr = 1,4-di(1,2,3-triazol-1-yl)butane, the iron(II) centers stay in the high-spin (HS)

253 For example, in the absence of butane, the major photoproduct is compound 5.

254 or (VO)2P2O7/SiO2 catalysts are exposed to n-butane, the rate of maleic anhydride formation is propor

255 e in the initial hydrogen abstraction from n-butane, the rate-determining step in the reaction sequen

256 r a range of temperatures (550-900 K) with n-butane, the simplest hydrocarbon fuel exhibiting cool fl

257 The studied hydrocarbon was n-butane, the smallest alkane which has an oxidation behav

258 ed cell performance after exposure to 25 cm3 butane, then recovered performance after 75 cm3.

259 r cracking in the case of both propane and n-butane; therefore, selectivity can be tuned by the selec

260 ain-release ring-opening of azabicyclo[1.1.0]butane to drive the equilibrium of the Brook rearrangeme

261 It reacts with butane to form a crystalline tBu(+) salt and with n-hexa

262 The selective oxidation of n-butane to maleic acid catalyzed by vanadium phosphates (

263 ys for the subsequent functionalization of n-butane to maleic anhydride and found that the overall ba

264 eaction intermediate for the conversion of n-butane to maleic anhydride under typical industrial cond

265 of thiophenes by insertion of bicyclo[1.1.0]butanes to produce eight-membered bicyclic rings under m

266 -4-methylsulfinyl-1-(S-methyldithiocarbamyl)-butane (trivial name, sulforamate), an aliphatic analogu

267 h affected adversely, but did not eliminate, butane utilization by P. butanovora.

268 mary alcohol dehydrogenases, BDH and BOH, in butane utilization in Pseudomonas butanovora (ATCC 43655

269 ible benzoylformate esters and bicyclo[1.1.0]butanes via visible-light-induced triplet energy transfe

270 The adsorption of n-butane was 10 times higher than methane by mole at 2 bar

271 bon oxides produced from fully (13)C-labeled butane were almost equal.

272 ne multi-carbon alkanes such as ethane and n-butane were described in both enrichment cultures and en

273 h rates of mutant strains G113N and L279F on butane were dramatically slower than the rate seen with

274 ption isotherms of propane, n-butane and iso-butane were measured to 8, 2, and 2 bar, respectively.

275 he adsorptions of propane, n-butane, and iso-butane were much higher than methane at the highest pres

276 al-to-central C-C bond cleavage ratios for n-butane were much larger on 8-MR than on 12-MR acid sites

277 -to-dehydrogenation ratios for propane and n-butane were much smaller and terminal-to-central C-C bon

278 ans-epoxysuccinyl-L-leucylamido-(4-guanidino)butane were without effect.

279 y generated cyclic allenes and bicyclo[1.1.0]butanes, which possess considerable strain energies of a

280 with either alkenes/alkynes or bicyclo[1.1.0]butanes, yielding cyclopent-anes/-enes and bicyclo[3.1.1