ライフサイエンスコーパス: bis

1 In this work, anticancer properties of bis (1,10-phenanthroline) silver (I) acetate monohydrate

2 partial PKC agonist isophthalate derivative bis(1-ethylpentyl) 5-(hydroxymethyl)isophthalate induced

3 erocyclic system is described wherein the 2H-bis([1,2,3]triazolo)[5,1-a:4',5'-c]isoquinoline ring sys

4 tential using the slow voltage-sensitive dye bis-(1,3-diethylthiobarbituric acid)trimethine oxonol re

5 ur findings from these studies show that 3,5-bis[(1E)-2(2,6-dichlorophenyl)ethenyl]-1H-pyrazole 2l 1)

6 n compounds bearing tridentate dianionic 2,6-bis(1H-1,2,4-triazol-5-yl)pyridine luminophoric pincer l

7 osulfonic acids A to D (9-12) are methyl 2,2-bis(1H-indol-3-yl) acetates.

8 3,3-Bis(2,4,6-triisopropylphenyl)-1,1-binaphthyl-2,2-diyl hy

9 alyst [Ir-IMes; [IrCl(COD)(IMes)], (IMes=1,3-bis(2,4,6-trimethylphenyl), imidazole-2-ylidene; COD=cyc

10 BDI(Mes)))(2)(mu-C(6)H(6))} (BDI(Mes) = N,N'-bis(2,4,6-trimethylphenyl)pentane-2,4-diiminate) with th

11 he case of K(2) [(NON)Al(NDipp)](2) (NON=4,5-bis(2,6-diisopropylanilido)-2,7-di-tert-butyl-9,9-dimeth

12 I) complex Re(eta(5)-Cp)(BDI) (1; BDI = N,N'-bis(2,6-diisopropylphenyl)-3,5-dimethyl-beta-diketiminat

13 s M(BDI(Dip)) (M = Al or Ga; BDI(Dip) = N,N'-bis(2,6-diisopropylphenyl)pentane-2,4-diiminate) in tolu

14 10 to +15% for polymers such as poly(2-(3,3'-bis(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)-[2,2'-bithiophe

15 lewheel-type MOF structure that contains 4,7-bis(2-(4-pyridyl)-ethynyl) isoindoline N-oxide and 1,4-b

16 yridyl)-ethynyl) isoindoline N-oxide and 1,4-bis(2-(4-pyridyl)-ethynyl)-benzene pillars that connect

17 erent permeability enhancers ethylene glycol-bis(2-aminoethylether)-N,N,N',N'-tetraacetic acid (EGTA)

18 [Co(bapbpy)Cl](+) (bapbpy: 6,6'-bis(2-aminopyridyl)-2,2'-bipyridine) is a polypyridyl co

19 (PAEs), such as dibutyl phthalate (DBP) and bis(2-ethyl hexyl) phthalate (DEHP), are now increasingl

20 different food matrices, including BPA, BPS, bis(2-ethylhexyl) adipate, dibutyl adipate, hexadecyl me

21 2-ethylhexyl 2,3,4,5-tetrabromobenzoate and bis(2-ethylhexyl) tetrabromophthalate among nBFRs.

22 stem PBDB-TF:Y6 (Y6 = 2,2'-((2Z,2'Z)-((12,13-bis(2-ethylhexyl)-3,9-diundecyl-12,13-dihydro-[1,2,5]thi

23 he considered alternatives were melamine and bis(2-ethylhexyl)-tetrabromophthalate.

24 Bis(2-ethylhexyl)ammonium (K(50) 29 uM), triisopentylamm

25 Migration of N,N-Bis(2-hydroxyethyl) alkyl(C8-C18)amines from five differ

26 ully synthesized from 5,5'-(propane-2,2-diyl)bis(2-hydroxyisophthalaldehyde) and 1,2-cyclohexanediami

27 onate, and two new compounds, namely (Z)-1,6-bis(2-hydroxyphenyl)-3,4-diphenylhex-3-ene-1,6-dione (D1

28 s(dicarboximide)-co-2,2'-bithiophene-co-N,N'-bis(2-octyldodecyl)-naphthalene-1,4,5,8-bis(dicarboximid

29 tive ligand (tBu,Tol)DHP ((tBu,Tol)DHP = 2,5-bis((2-t-butylhydrazono)(p-tolyl)methyl)-pyrrole) activa

30 N cells with another GLS-exclusive inhibitor bis-2'-(5-phenylacetamide-1,3,4-thiadiazol-2-yl)ethyl su

31 d-surfactant 1-butyl-3-methylimidazolium 1,4-bis-2-ethylhexylsulfosuccinate (bmim-AOT).

32 hose found for RMs generated with sodium 1,4-bis-2-ethylhexylsulfosuccinate (Na-AOT).

33 Sorption mechanism of uranyl by poly(bis[2-(methacryloyloxy)ethyl] phosphate) (PB2MP) functio

34 dihyride complex (PNP)Ir(H)(2) (IrN 1, PNP = bis[2-diisopropylphosphino)ethyl]amide).

35 rsibly responsive transformation between the bis[2]catenane and the bis-metallacage can be realized b

36 Herein, a cyclic bis[2]catenane is constructed through the coordination-d

37 ectrometry confirm the formation of a cyclic bis[2]catenane with "infinity"-shaped topology via a 14-

38 2,2-diphenyl-1-picrylhydrazyl and 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonic) acid assays show

39 tructed by linking the fullerene (C(60)) and bis(3,4,5-trimethoxyphenyl)aniline (BTMPA) to the alumin

40 n N-benzyl BINOL-phosphoramidite and a BINAP-bis(3,5-t-Bu-aryl)phosphine, are addressed through exhau

41 ysilane, (3-Aminopropyl)triethoxysilane, 1,3-Bis(3-aminopropyl)-1,1,3,3-tetramethyldisiloxane, reachi

42 ABTS, 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate), is a common chr

43 the 3,5-dinitrosalicylic acid and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic) acid assays.

44 me-peptide fragment then oxidized 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) to g

45 p)(2)](2+) photosensitizer, where bmip = 2,6-bis(3-methyl-imidazole-1-ylidine)-pyridine, with simulta

46 atization strategy to convert the simple 1,4-bis(3-pyridyl)butadiynes 3a,b into the fjord-edge nitrog

47 Using poly[2,5-bis(3-tetradecylthiophen-2-yl) thieno[3,2-b]thiophene] a

48 The second messenger bis-3,5-cyclic di-guanosine monophosphate (c-di-GMP) det

49 nd releases high levels of the STING agonist bis-(3'-5')-cyclic dimeric adenosine monophosphate (c-di

50 e kinetics of the benzoate transfer from the bis(4-dimethylamino)-substituted benzhydryl benzoate Ar(

51 erpenetrated Hf MOF, linked by 1,4-phenylene-bis(4-ethynylbenzoate) ligands (Hf-peb), are induced by

52 Thus, a series of bis(4-fluorophenyl)methyl)sulfinyl)alkyl alicyclic amine

53 In rats, 1-(4-(2-((bis(4-fluorophenyl)methyl)sulfinyl)ethyl)-piperazin-1-yl

54 In this study, 3,3-bis(4-hydroxy-3-((E)-((4-hydroxyphenyl)imino)methyl) phe

55 4"'-(pyrazine-2,3,5,6-tetrayl) tetrakis (N,N-bis(4-methoxyphenyl) aniline) (PT-TPA) which can effecti

56 sidered the repurposing of (11)C-labeled 1,5-bis(4-methoxyphenyl)-3-(2,2,2-trifluoroethoxy)-1H-1,2,4-

57 Copper(II)-diacetyl-bis(4-methylthiosemicarbazonato) (Cu-ATSM) is a PET trac

58 l (CB7) catalyzes the hydrolysis reaction of bis(4-nitrophenyl)carbonate (1) but inhibits that of bis

59 trophenyl)carbonate (1) but inhibits that of bis(4-nitrophenyl)thiocarbonate (2).

60 ole-transporting large-bandgap polymer (poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine (PTAA)) is emp

61 (RSE) below 3% for aqueous solutions of 1,2-bis(4-pyridyl)ethylene (BPE), the lowest reported to dat

62 f the new complex, which incorporates a N,N'-bis(4-pyridylmethyl)-1,6-hexanediamine tether ligand, ar

63 symbolic methacrylate-based dental resins-2-bis[4-(2-hydroxy-3-methacryl-oxypropoxy)-phenyl]-propane

64 loped a novel c-Myc-targeting compound, N, N-bis (5-ethyl-2-hydroxybenzyl) methylamine (EMD), and pre

65 examined the effect of a new compound, N, N-bis (5-ethyl-2-hydroxybenzyl) methylamine (EMD), in targ

66 [3,2-b]indole-2,10-diyl)bis(methanylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylide

67 (2-) is the doubly deprotonated form of [2,6-bis(5-(2,4,6-trimethylphenyl)-3-phenyl-1H-pyrrol-2-yl)py

68 ford the new dibrominated bis-indole ketone, bis(6-bromo-1H-indol-3-yl)methanone (3), followed by N-s

69 separated from the 19 structural isomers of bis[60]phenyl-C61-butyric acid methyl ester, using them

70 dmixed with the conjugated polymer poly(N,N'-bis(7-glycol)-naphthalene-1,4,5,8-bis(dicarboximide)-co-

71 posed of NIPAm, degradable crosslinker N, N'-bis (acryloyl) cystamine (BAC), sulfated 2-acrylamido-2-

72 lopropylmethyl) bearing a bulky bidentate 2-[bis(adamant-1-yl)phosphino]phenoxide ligand (L).

73 photoswitching on the regiochemistry of the bis-addition, have been studied.

74 The formation of the bis-adducts and their spectroscopic and photochemical pr

75 sures the PSD reaction using distyrylbenzene-bis-aldehyde (DSB-3), whose reaction with PE produces a

76 lene compound resulted in the isolation of a bis(alkyne) zirconocene complex instead(6).

77 The resulting rhodium(III) bis(alkynyl) product can be trapped out by reaction with

78 deuteration that reinforces oxidation-prone, bis-allylic sites of PUFAs is a novel, nonantioxidant tr

79 lato)diborane (B(2)neop(2)) mediated by iron-bis amide is described.

80 , through the reactions of the corresponding bis(amides), M{N(SiMe(3) )(2) }(2) (thf)(2) , with (thf)

81 (ESR) measurements measurements of pristine, bis-, and tris-adducts of Gd(3)N@C(80) suggested that th

82 r study also reveals the mechanisms by which bis-ANS and related compounds modulate LLPS and identify

83 Depending on context, bis-ANS can both induce LLPS de novo as well as prevent

84 ylene in contrast to the previously reported bis(aryl)stannylene.

85 clization, [1,5]-hydride shift of conjugated bis-aryl cycloalkenone substrates.

86 These reactions yield 1,3-bis(arylamino) and 1,3-bis(arylthio and alkylthio)indane

87 which we measure the host-guest binding of a bis(arylethynyl phenylurea) host with a chloride guest i

88 at room temperature to furnish symmetrical (bis)aryls in good yields under mild reaction conditions.

89 e reactions yield 1,3-bis(arylamino) and 1,3-bis(arylthio and alkylthio)indanes, respectively, which

90 In addition, the encapsulation of bis-aza[60]fullerene (C(59)N)(2) within a supramolecular

91 Room temperature photolysis of the bis(azide)cobaltate(II) complex [Na(THF)(x)][((ket)guan)

92 and volumetric properties of DB1976, a model bis(benzimidazole)-selenophene diamidine compound with e

93 mbinatorial screening approach to identify a bis-benzodioxolylindolinone (azoffluxin) that synergizes

94 ne (D1) and (Z)-2,2'-(1,2-diphenylethene-1,2-bis(benzofuran-3(2H))-one) (D2), obtained in significant

95 Here we present a pyrazolate-based bis(beta-diketiminato) ligand [L(Ph)](3-) with bulky m-t

96 different catalytic cycle, iodine yields the bis-bisulfate ester of ethylene glycol (HO(3)SO-CH(2)-CH

97 or the monoprotodeboration of beta-amino gem-bis(boronate) precursors.

98 ondensation of easy manageable lithium alpha-bis(boryl)carbanions with carbonyl derivatives, the so-c

99 ollowed by C-H borylation to provide geminal bis-borylated products.

100 roviding high yield of the mono- and geminal bis-borylation products.

101 electrochemical study indicated that dithia-bis(calix)-sapphyrins are relatively easier to reduce bu

102 hromic shifts observed for protonated dithia-bis(calix)-sapphyrins macrocycles.

103 However, the protonated dithia-bis(calix)-sapphyrins showed large bathochromic shifts i

104 ing that the electronic properties of dithia-bis(calix)-sapphyrins were altered significantly upon pr

105 The DBF/DBT-embedded dithia-bis(calix)-sapphyrins were characterized by HRMS (high-r

106 (DBF)/dibenzothiophene (DBT)-embedded dithia-bis(calix)-sapphyrins were synthesized by condensing 1 e

107 matographic purification afforded new dithia-bis(calix)-sapphyrins with two meso-sp(3) carbons in 5-7

108 red significantly upon protonation of dithia-bis(calix)-sapphyrins.

109 This was achieved by bis-carbonylation at C-3 of the magnesium salt of 6-brom

110 xperiments revealed bis(phosphine)cobalt(II) bis(carboxylate)s were generated in catalytic reactions

111 sis of PiuA Fe(III)-bis-catechol and Ga(III)-bis-catechol and Ga(III)-(NE)(2) complexes by NMR spectr

112 Structural analysis of PiuA Fe(III)-bis-catechol and Ga(III)-bis-catechol and Ga(III)-(NE)(2

113 entate Fe(III) complexes formed by mono- and bis-catechol species are important Fe sources in Gram-po

114 straction and alkane elimination to form the bis-cyclometalated derivatives [Ru(PPh(3))(C(6)H(4)PPh(2

115 geometry of 2 is that of a perfectly linear bis(cyclopentadienyl) sandwich complex, with the ground-

116 Bis(cyclotryptamine) alkaloids have been popular topics

117 Five possible scaffolds for bis(cyclotryptamine) alkaloids were originally postulate

118 Thus, we suggest the utilization of bis-deoxygalactosyl-carborane building blocks in solid p

119 sent the successful introduction of multiple bis-deoxygalactosyl-carborane building blocks to the GRP

120 plex ((tBu)POCOP)Re(CO)(2) ((tBu)POCOP = 2,6-bis(di-tert-butylphosphinito)phenyl) that catalyzes CO(2

121 We discovered that 3,3-bis-di(methylsulfonyl)propionamide (3bMP1) inhibits the

122 of 1,6,7,12-tetra(phenoxy)perylene-3,4:9,10-bis(dicarboximide) having either n-octyl groups (octyl-t

123 N,N'-bis(2-octyldodecyl)-naphthalene-1,4,5,8-bis(dicarboximide), and found to act as a simultaneous m

124 poly(N,N'-bis(7-glycol)-naphthalene-1,4,5,8-bis(dicarboximide)-co-2,2'-bithiophene-co-N,N'-bis(2-oct

125 olorimetric sensor using synthesized 3', 6'- bis(diethylamino) -2- ((3,4,5 trimethyl benzylidene) ami

126 on catalyzed by [Pt(depe)(2) ](2+) (depe=1,2-bis(diethylphosphino)ethane).

127 Emmons (HWE) reaction of C(2) -symmetric 1,4-bis(diethylphosphonomethyl)benzene or 4,4'-bis(diethylph

128 4-bis(diethylphosphonomethyl)benzene or 4,4'-bis(diethylphosphonomethyl)biphenyl with C(3) -symmetric

129 his Article describes the development of 1,2-bis(diisopropylamino)-3-cyclopropenylium-functionalized

130 We deposit bis(diisopropylamino)cyclopropenylidene (BAC) on Au(111)

131 ]} (1; xant(P(i)Pr(2))(2) = 9,9-dimethyl-4,5-bis(diisopropylphosphino)xanthene) coordinates the Si-H

132 (2)]} (xant(P(i)Pr(2))(2) = 9,9-dimethyl-4,5-bis(diisopropylphosphino)xanthene).

133 aH) in acetonitrile greater than that of 1,8-bis(dimethylaminonaphthalene) (DMAN), although its synth

134 n of mixed-valence class II and class II-III bis(dioxolene) bridging ligands with sufficiently weak i

135 egree of electronic communication within the bis(dioxolene) ligand and (2) the matching of cobalt and

136 Bis(dioxolene)-bridged dinuclear cobalt compounds provid

137 eeds an expensive small molecule such as 2,8-bis(diphenyl-phosphoryl)dibenzo[b,d]thiophene (PPT) as t

138 )(dppe)H](+) (Cp* = C(5)Me(5)(-), dppe = 1,2-bis(diphenylphosphino)ethane), to a highly reactive, S =

139 ands, [Au(22) H(4) (dppo)(6) ](2+) [dppo=1,8-bis(diphenylphosphino)octane].

140 (30) (dppm)(10) Cl(10) ](4+) (SD/Ag78a; dppm=bis-(diphenylphosphino)methane) that was synthesized thr

141 yrophosphate (PP-InsP) signaling family: 1,5-bis-diphosphoinositol 2,3,4,6-tetrakisphosphate (InsP(8)

142 (tBu)dmx: dimethylxanthine-bridged, cofacial bis-dipyrrin) were synthesized by deprotonation/metalati

143 ramolecular structures of cholesteryl-linked bis(dipyrrinato)zinc(II), to an exceptionally high level

144 l P-based key intermediates including a 1,4-(bis)electrophilic alpha,beta-unsaturated ketenyl phospho

145 and chain-extended through the formation of bis(eta(2)-alkyne)Pt(0) complexes.

146 te (EDBE)PbBr(4) (EDBE = 2,2'-(ethylenedioxy)bis(ethylammonium)) behaves as a single ensemble.

147 amily of metal dichloride complexes having a bis-ferrocenyl-substituted pyridinediimine ligand was sy

148 -benzene ring with fluorine scan of mono- or bis-fluorine atoms around DRV's scaffold.

149 zolium (EMIm) cations and high-concentration bis(fluorosulfonyl)imide (FSI) anions, with sodium bis(t

150 Al@Al is fully wetted by a 4 m potassium bis(fluorosulfonyl)imide-dimethoxyethane electrolyte (th

151 and Z isomers, indicating that the covalent bis-functionalization of C(60) can be controlled by ligh

152 We report the synthesis of a series of bis-functionalized beta-peptoid oligomers of the hexamer

153 oxy-3-methacryl-oxypropoxy)-phenyl]-propane (Bis-GMA) and 2-hydroxyethyl-methacrylate (HEMA)-and have

154 es were relatively more hydrophobic than the Bis-GMA/HEMA controls.

155 ced approximately 89% in comparison with the Bis-GMA/HEMA controls.

156 They were compared with Bis-GMA/HEMA-based commercial and experimental dental ad

157 ne resulted in the formation of a conjugated bis-guanidinate (CBG)-supported aluminum dihydride compl

158 Three new dimeric bis-guanidinate zinc(II) alkyl, halide, and hydride comp

159 lyamine biosynthesis inhibitor methylglyoxal bis-(guanylhydrazone) (MGBG), but the molecular defects

160 An efficient new synthesis of 3,5-bis(het)arylisoxazoles, involving the reaction of 1,3-bi

161 rylisoxazoles, involving the reaction of 1,3-bis(het)arylmonothio-1,3-diketones with sodium azide in

162 amides, esters, (hetero)aromatic ynones, and bis(hetero)aryl ketones were synthesized in good-to-exce

163 Reductive elimination therefrom provides bis-heteroaryl products in a practical and efficient fas

164 is-pyrazoles as well as other pyrazole-based bis-heterocyclic molecules were prepared in moderate to

165 ))-H-C(sp(2)) bond in order to prepare novel bis-heterocyclic scaffolds.

166 gen at room temperature to yield the elusive bis-hydridogermylene [(ADC(Ph))GeH](2) (5).

167 Reduction of a dicopper(II) bis(hydroxide) complex with silanes in the presence of e

168 different FARs [diazolidinyl urea (DAU), 1,3-bis(hydroxymethyl)-5,5-dimethylimidazolidine-2,4-dione (

169 s-coupling strategy is used to construct the bis-imidazolyl core skeleton.

170 by facile one-electron oxidation of an Fe(V) bis(imido) (2).

171 hich leads to the exclusive formation of the bis(imido) complexes [((ket)guan)Co(mu-NH)](2) (6) and [

172 tructures of the sponge-derived dibrominated bis-indole alkaloids, namely, echinosulfone A (2) and th

173 h triphosgene to afford the new dibrominated bis-indole ketone, bis(6-bromo-1H-indol-3-yl)methanone (

174 mate and are all carbon-bridged dibrominated bis-indoles: echinosulfone A (2) is a di(1H-indol-3-yl)m

175 presence of a trithiocarbonate and 2,2'-azo-bis isobutyro nitrile (AIBN) in toluene solution under a

176 ignificant concentrations of 5-coordinate Si bis-ligand complex being detected even under biologicall

177 ore effective than a previously used complex bis(maltolato)oxovanadium(V) in neuroblastoma cell lines

178 formation between the bis[2]catenane and the bis-metallacage can be realized by guest exchange, conce

179 tion-driven self-assembly of the interlocked bis-metallacage, by the 90 degrees Pt(II) heteroligation

180 eno[2',3':4,5]-thieno[3,2-b]indole-2,10-diyl)bis(methanylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-

181 Derivatives of (-)-1, i.e., the bis-methylated diamine (+)-5 and two diastereomeric tric

182 The first examples of bis-modified, bacteriochlorin-type PMPs containing eithe

183 An accurate accelerated design of bis-MPA monomers with orthogonally complementary moietie

184 the Lewis acid Sc(3+) and transforms into a bis(mu-oxo)diiron(IV) complex, thus providing a syntheti

185 sMMO-Q was previously reported as a bis-mu-oxo Fe(IV)(2)(mu-O)(2) diamond core but was recen

186 -like intermediate (high-valent diamond-core bis-mu-oxo-[Fe(IV)](2) unit) is involved in the reaction

187 ith a recently reported ligand, pyridine-2,6-bis(N-cyanocarboxamidine) (PyBCam(CN)).

188 nd PBP pincer complexes of Rh with a central bis(N-pyrrolyl)aluminyl or -boryl unit.

189 ort a rationally designed redox-active Au(I) bis-N-heterocyclic carbene that induces ICD both in vitr

190 preparation of asymmetric redox-active Au(I) bis-N-heterocyclic carbenes.

191 ylation of alkyl bromides and chlorides with bis(neopentylglycolato)diborane (B(2)neop(2)) mediated b

192 A 1,2 bis(o-aminophenoxy)ethane-N,N,-N',N'-tetraacetic-acid-ba

193 l-1,4,8,11-tetraazacyclotetradecane-1,8-diyl)bis(octadecan-2-ol) ([Co(L3)](2+) ) were synthesized to

194 teroarenes through challenging unsymmetrical bis-olefination process in a one-pot sequential fashion.

195 AP) and N-(4-carboxybenzyl)-N,N-dimethyl-2,3-bis(oleoyloxy)propan-1-aminium (DOBAQ).

196 octadecanes via condensation reaction of 1,4-bis(organylphosphino)butane, formaldehyde, and primary a

197 We quantitatively establish the advantage of bis- over mono-intercalators before demonstrating the ap

198 The protocol was enabled by a new bis(oxazoline) (BOX) ligand designed via a rapid structu

199 recently introduced simple chiral ruthenium bis(oxazoline) (pybox) complex ( Angew.

200 Dinickel naphthyridine-bis(oxazoline) catalysts promote enantioselective interm

201 E, here we created seven uncharged acetamido bis-oximes as candidate antidotes.

202 of several CNS-directed, uncharged aliphatic bis-oximes holding promise for use as protonation-depend

203 heterocyclic amines and oxime groups of the bis-oximes resulted in equilibration among up to 16 dist

204 Both oxime groups in these bis-oximes were attached to the same central, saturated

205 Oxime group reorientation of one of the bis-oximes, forcing it to point into the active center f

206 1,1,1-Trichloro-2,2-bis(p-chlorophenyl)ethane (DDT) and its metabolites had

207 designing a catalyst for a model substrate (bis-p-nitrophenylphosphate) may provide wrong indication

208 nists are lipopeptides possessing the S-[2,3-bis(palmitoyloxy)propyl]-l-cysteine (Pam(2)Cys) motif an

209 ated carboxylic acids using readily prepared bis(phosphine) cobalt(0) 1,5-cyclooctadiene precatalysts

210 A series of bis(phosphine) cobalt(II) bis(pivalate) complexes, which

211 Bis(phosphine) copper hydride complexes are uniquely abl

212 X-band EPR experiments revealed bis(phosphine)cobalt(II) bis(carboxylate)s were generate

213 hydroxo-[2,2':6',2''-terpyridine]-6,6''-diyl)bis(phosphonate) ligand.

214 structures of 14-3-3sigma bound to mono- and bis-phosphorylated APN-derived peptides, which revealed

215 molecule that acts as receptor for mono- and bis-phosphorylated PIPs in a cell free environment.

216 A novel bis-pillar[5]arene dicarboxylic acid self-assembles in t

217 readily generated by reaction of commercial bis(pinacolato)diboron with alkyl Grignard compounds.

218 A series of bis(phosphine) cobalt(II) bis(pivalate) complexes, which bear structural similarit

219 ntials (V(on)) by synthesizing a specialized bis-PNP macrochelate that enables one-step Ni(II) bindin

220 2,3,9,10,16,17,23,24-Octakis (4-methyl-2,6-bis((prop-2-yn-1-yloxy)methyl)phenoxy) phthalocyaninato

221 l-1,4,8,11-tetraazacyclotetradecane-1,8-diyl)bis(propan-2-ol) ([Co(L2)](2+) ), and 1,1'-(4,11-dibenzy

222 om temperature and furnishes the pyrazine or bis-pyrazine-containing condensation products in good to

223 Using the doubly protic bis-pyrazole-pyridine ligand (N(NN(H))(2)), we have synt

224 tions, and various symmetric and unsymmetric bis-pyrazoles as well as other pyrazole-based bis-hetero

225 Bis(pyrazolyl)alkanes are a prolific class of ligands fo

226 ysis, accessible by the condensation between bis(pyrazolyl)methanones and carbonyls.

227 ptimal nitrogen-nitrogen distance, bidentate bis(pyridine)-Au(III) complexes convert into dimers.

228 For the first time, bis(pyridine)Au(I) complexes are shown to be catalytical

229 hods for the formation of unsymmetrical 2,2'-bis-pyridines are scarce.

230 sed of two covalently strapped electron-rich bis-pyrrolidine PDI panels, nicknamed the "Green Box" du

231 zing distinct plant phenol-derived mono- and bis-quinone methide intermediates during different C-C a

232 y ligand scrambling, to form 1 and the U(VI) bis(silsesquioxane) complex, [U(Cy(7)Si(7)O(12))(2)] (3)

233 droxylation of sulfonylcyclopropanes using a bis(silyl) peroxide as the electrophilic oxygen source.

234 of 2 with silver(I) yields the monocationic bis(silylene) N(I) complex 4 with the closo-C(2) B(10) c

235 mediated by two divalent silicon atoms in a bis(silylene) scaffold, resulting in a silylene-stabiliz

236 nits are regenerated to furnish the isolable bis(silylene)-stabilized N(I) complex as an anion of 3 w

237 The first series of bis(silylene)-stabilized nitrogen(I) compounds is descri

238 tom to the C(2)B(10) core to form an elusive bis(silylene)-stabilized Si(I) radical cation which unde

239 d from the redox reaction of the dipotassium bis(silylenyl)-nido-carboranate salt, 1,2-(LSi)(2)-1,2-C

240 lex ("silylone") stabilized by the chelating bis(silylenyl)-ortho-carborane ligand, 1,2-(LSi)(2)-1,2-

241 oach for the stereoselective construction of bis-spiroketals with thermodynamically similar stereoiso

242 ve flavylium salts (50-80%) or thermochromic bis-spiropyrans (73%).

243 singly, two of these structurally simple 3,5-bis(styryl)pyrazoles (2a and 2l) had concentrations whic

244 rotocol, we have synthesized a number of 3,5-bis(styryl)pyrazoles 2a-l, thus allowing for their scree

245 ken together, these results suggest that 3,5-bis(styryl)pyrazoles warrant further investigation as le

246 stigation of the mechanism of action of some bis(styryl)pyrazoles, demonstrating their potential as l

247 e hydroquinone cyclosiphonodictyol A and its bis(sulfato) from commercial (+)-sclareolide is reported

248 In contrast, sterically hindered bis-sulfonamides and related nucleophiles reacted with B

249 2,5-Bis(tert-butyldimethylsilyloxy)furans are established as

250 ding benzynes, is also demonstrated, and 2,5-bis(tert-butyldimethylsilyloxy)pyrroles are established

251 n processing a soluble derivative of QA, N,N-bis(tert-butyloxycarbonyl)-quinacridone (TBOC-QA), follo

252 the synthesis of a stereochemically-defined bis-tetrahydrofuran (bis-THF) derivative, which is one o

253 d HIV-1 protease inhibitors (PIs) containing bis-tetrahydrofuran (bis-THF) in a pseudo-C(2)-symmetric

254 nsights into optimizing HIV-1 PIs containing bis-THF in non-sulfonamide dipeptide isosteres.

255 vity relationship studies indicated that the bis-THF moiety can be attached at either the P2 or P2' p

256 ies of PIs were synthesized by incorporating bis-THF of darunavir on either side of the Phe-Phe isost

257 tereochemically-defined bis-tetrahydrofuran (bis-THF) derivative, which is one of the key structural

258 bitors (PIs) containing bis-tetrahydrofuran (bis-THF) in a pseudo-C(2)-symmetric dipeptide isostere a

259 anethiols (Alk-SH) provide the corresponding bis-thiolated indole derivatives.

260 ydes and ketones, the reaction scope for 3,6-bis(thiomethyl)-1,2,4,5-tetrazine, a survey of participa

261 n reactions promoted by a precisely tailored bis-thiourea hydrogen-bond-donor catalyst.

262 ble selectivities to our previously reported bis-thiourea ortho-selective catalyst, with a catalyst l

263 We report highly beta-selective bis-thioureas-catalyzed 1,2-cis-O-pyranosylations employ

264 ogen bond (ChB) donors integrated into a 3,5-bis-triazole pyridine structure covalently linked to ben

265 uble organic semiconductor 2,8-Difluoro-5,11-bis(triethylsilylethynyl)anthradithiophene (diF-TES-ADT)

266 Using 2,8-difluoro-5,11-bis(triethylsilylethynyl)anthradithiophene (Dif-TES-ADT)

267 action, with the derivatising agent N-methyl-bis-trifluoroacetamide, to substitute the exchangeable h

268 droxy compounds with iodobenzene diacetate, [bis(trifluoroacetoxy)]iodobenzene, and ammonium cerium(I

269 has been developed using the combination of bis(trifluoroacetoxy)iodobencene and trimethylsilyl brom

270 uorosulfonyl)imide (FSI) anions, with sodium bis(trifluoromethanesulfonyl)imide (NaTFSI) as a key add

271 lvation sheath of lithium ions enabling more bis(trifluoromethanesulfonyl)imide anion (TFSI(-) ) to c

272 n combined with a flexible triamine and zinc bis(trifluoromethanesulfonyl)imide, this ketone formed a

273 fferentiation experiments using alpha,alpha'-bis(trifluoromethyl)-9,10-anthracenedimethanol (ABTE) as

274 yphenyl) and Ar(F)-P=CPh(2) [1b: Ar(F) = 2,6-bis(trifluoromethyl)phenyl] have been prepared, isolated

275 ybenzamide (1, IC(50) 0.0192 muM) and N-[3,5-bis(trifluoromethyl)phenyl]-4-chloro-2-hydroxybenzamide

276 The most potent compounds, N-[3,5-bis(trifluoromethyl)phenyl]-5-chloro-2-hydroxybenzamide

277 3-h]phenazine (bpph) and dCF(3)ppy is 2-(3,5-bis(trifluoromethyl-phenyl)pyridine), were found to be r

278 cid (PSA), and benzoic acid (BA) using N-3,5-bis-(trifluoromethyl)-phenyl-N-4-vinylphenyl urea (1) as

279 onic liquid (IL) 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (BmimNTf(2)) as a func

280 an ionic liquid, 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, and poly(vinylidene f

281 When 6,13-bis(triisopropylsilylethynyl) pentacene (TIPS pentacene)

282 We found that bis(triisopropylsilylethynyl)pentacene (TIPS-P) crystals

283 ounts of organosilica precursor, namely, 1,2-bis(trimethoxysilyl)ethane.

284 M-SEGPHOS, a bisphosphine ligand bearing 3,5-bis(trimethylgermanyl)-4-methoxyphenyl groups as the sub

285 hosphine ligand (TMG-SYNPHOS) containing 3,5-bis(trimethylgermanyl)phenyl groups on phosphorus and ap

286 Complexes of bis(trimethylsilyl)acetylene Me3SiC2SiMe3 (mono-function

287 e and TMS(2)S by the conjugate base, lithium bis(trimethylsilyl)amide (LiN(SiMe(3))(2)), and elementa

288 The method relied on lithium bis(trimethylsilyl)amide-mediated intramolecular cycliza

289 Tris[N,N-bis(trimethylsilyl)amide]lanthanum (La(NTMS)) is an effi

290 2H)] (1, (TMS)PS2H(2) = 2,2'-dimercapto-3,3'-bis(trimethylsilyl)diphenyl)phenylphosphine; H is a diss

291 responding pyrophoric primary phosphines and bis(trimethylsilyl)phosphines, have been isolated and ch

292 The anion [P(4)O(11)](2-), employed as its bis(triphenylphosphine)iminium (PPN) salt, is shown here

293 igold complexes of the general formula R-1,5-bis-triphenylphosphinegold(I) 1,2,3-triazolate (Au(2)-R)

294 selective ring opening with CsF and a chiral bis-urea catalyst.

295 phere at zirconium, imparted by the tethered bis(ureate) ligand, is crucial for the coordination of n

296 f alpha,beta-unsaturated ketones to generate bis-vinyl sulfides.

297 Reduction of the bis-vinylimidazole delivered the core framework of nagel

298 n readily achieved in two steps from a known bis-Weinreb amide derived from l-tartaric acid.

299 is(xanthylium)-biphenylene ([3](2+)) and 4,5-bis(xanthylium)-9,9-dimethylxanthene ([4](2+)) which pro

300 e studies are the bifunctional dications 1,8-bis(xanthylium)-biphenylene ([3](2+)) and 4,5-bis(xanthy