ライフサイエンスコーパス: imide

1 d carbonylation and ring closure to form the imide.

2 chlorin-isoimide in addition to the chlorin-imide.

3 a hydrogen storage mechanism for the ternary imide.

4 mpact on the hydrogenation properties of the imide.

5 ethyl-3-methylimidazolium bis(fluorosulfonyl)imide.

6 rst (15) N NMR resonance recorded on an iron imide.

7 this reaction on unsymmetrically substituted imides.

8 ment of regioselectively reduced N-homoallyl imides.

9 aldehydes, ketones, esters, carbamates, and imides.

10 possibility to successfully ionize PAHs and imides.

11 of the bis(imino)pyridine alkyl-substituted imides.

12 ed Julia olefination previously developed on imides.

13 -4-alkenyl- and 3-hydroxy-2-methyl-4-alkenyl imides.

14 Nickel-imide 1 competes with the nickel-amide HAA product [Me(3

15 H by 1 to give R(*), which may add to either imide 1 or amide 2, each featuring significant N-based r

16 magnetically coupled to an imidyl radical (S(imide) = 1/2) and a closed-shell, dianionic bis(imino)py

17 ether adduct of an asymmetric niobium(V) bis(imide) 2.OEt2 containing the monoazabutadiene (MAD) liga

18 c(Me){NHB(NAr'CH)2} (18) generated transient imide 25 via rate-determining, first-order methane elimi

19 dergo a new rearrangement to cyanopyridine N-imide 40 with an activation energy of 43 kcal/mol.

20 nusual complexes including the ruthenium(IV) imide, 7-OMe, as well as the Ru(II) azide adduct 8-OMe.

21 ahydrofuran and the mononuclear Ta(V) parent imide 8 in toluene.

22 Complex 2 equilibrated back to the imide A-py slowly, as the isotopomer (PNP)Sc(ND[DIPP])(e

23 e of the C-H of phenylacetylene to yield the imide acetylide [{((Me(3)Si)(2)N)(2)U(THF)}(2)(mu-N)][((

24 and 7,12-di-phenoxy bay substitution at the "imide-activated" 7- and 12-bay positions of 1,6,7,12-tet

25 ononitrile are much more stable than lithium imides, alane binding dramatically reduces the enamide p

26 formation of the bis(imino)pyridine vanadium imide amide compounds, ((iPr)BPDI)V(NHAr)NAr, were obser

27 SBimide is an imide analogous to the imide forms of other citric acid

28 thylimidazolium bis(trifluoromethanesulfonyl)imide and 1-butyl-3-methylimidazolium bis(trifluorometha

29 Moreover, one-step construction of imide and amide bonds with a long-chain alkyl group is a

30 olerant to the diverse functionality of both imide and halide units.

31 xyuridine without the protection at the N(3)-imide and provides a facile and general access to versat

32 oxy-PBI (compound 15) that has two different imide and three different bay substituents.

33 ese intermediates are easily hydrolyzed into imides and amides through vanadium catalysis.

34 ified that enables their transformation into imides and amides.

35 The resulting chlorin-imides and chlorin-isoimides exhibit long-wavelength abs

36 Atropisomeric enone-imides and enone-amides featuring N-CAryl bond rotation

37 thod for the synthesis of various naphthalic imides and perylene diimides (PDIs) using twin-screw ext

38 oxyethane, TFSI=bis(trifluoromethanesulfonyl)imide) and realize the best cycling stability among all

39 ethylimidazolium bis(trifluoromethylsulfonyl)imide, and poly(vinylidene fluoride-co-hexafluoropropyle

40 e utility of this method to generate amides, imides, and carbamates is illustrated by a one-pot synth

41 both aryl- and alkyl-substituted nickel(III)-imides, and examples of both types have been isolated an

42 including alkenes, alkynes, esters, amines, imides, and O-, S-, and N-heterocycles.

43 alently attached to a 4-aminonaphthalene-1,8-imide (ANI) chromophore and a naphthalene-1,8:4,5-bis(di

44 s enabling more bis(trifluoromethanesulfonyl)imide anion (TFSI(-) ) to coordinate with Li(+) ions.

45 (14,15)N ENDOR measurements of the bridging imide are consistent with an allyl radical molecular orb

46 tion/intramolecular cyclization of azolium N-imides are reported.

47 iquids (IL) with bis(trifluoromethylsulfonyl)imide as counterion for lubrication.

48 he discovery of tert-leucinol derived cyclic imides as a potent series of novel P3 capping groups.

49 With use of a chiral ligand and imides as carbon nucleophiles, a 3,4-addition protocol w

50 Here, we introduce benzo[ghi]perylene imides as new organic photoredox catalysts for Birch red

51 We report on cyclic imides as weak directing groups for selective monohydrox

52 ld synthetic approach to access a variety of imides as well as amides in high yields.

53 he protection of the NH group of a series of imides, azinones (including AZT), inosines, and cyclic s

54 olymers and poly(tert-butyl ester norbornene imide-b-N-methyloxanorbornene imide) copolymers were pre

55 thylimidazolium bis(trifluoromethanesulfonyl)imide, background subtraction is necessary at a macrodis

56 provides a facile entry into a new class of imide-based "3 + 3" macrocyclic trimer (trezimide), toge

57 Here, we report imide-based degrader molecules capable of degrading both

58 KZF3), which are well-established targets of imide-based degraders.

59 capacity to capture low-concentration CO2 by imide-based ionic liquids.

60 Although it shares a binding site with other imide-based natural product translation inhibitors, CL e

61 report a new type of SPC based on a [2 + 3] imide-based organic cage (NKPOC-1) and find that it exhi

62 nolates to alpha,beta-unsaturated esters and imides bearing adjacent stereocenters (X, Y = H, Me, OR)

63 hylimidazolium bis(trifluoromethanesulfonyl)-imide, BMI(Tf2N), has been developed and characterized f

64 ethylimidazolium bis(trifluoromethylsulfonyl)imide (BMIm-TFSI), and some combination of ferrocene (Fc

65 ethylimidazolium bis(trifluoromethylsulfonyl)imide (BmimNTf(2)) as a function of surface charge densi

66 ethylimidazolium bis(trifluoromethylsulfonyl)imide (BmimNTf2) were investigated with two-dimensional

67 hylpyrrolidinium bis(trifluoromethylsulfonyl)imide (BMP TFSI) and dimethylformamide.

68 ylpyrrolidinium-bis(trifluoromethanesulfonyl)imide (BMP-TFSI) IL is beneficial for glucose detection,

69 hylpyrrolidinium bis(trifluoromethylsulfonyl)imide ([Bmpyr](+)[NTf2](-)).

70 omerization about a highly conserved Trp-Pro imide bond in a region of the TAD that is required for n

71 The imide bond is twisted, and the O horizontal lineC-N-C(O)

72 The measured Fe-N(imide) bond distance (1.768(2) A) is the longest reporte

73 planar compounds with relatively short Fe-N(imide) bond lengths and two-electron reduction of the re

74 temperatures via rotation about a C(aryl)-N(imide) bond of a carboxylic acid monomer.

75 of restricted rotation around that C(aryl)-N(imide) bond, which locks the carboxylic acid recognition

76 amines on proteins to yield stable amide or imide bonds.

77 dral oligomeric silsesquioxanes and aromatic imide bridges.

78 olium)dodecane bis[(trifluoromethyl)sulfonyl]imide bromotrichloroferrate(III) ([(C16BnIM)2C12(2+)][NT

79 Bithiophene imide (BTI) and benzodithiophene (BDT) copolymers are sy

80 tion for the desymmetrization of meso-cyclic imides by hydrogenation with 8-K are also described here

81 pentadienyl) titanium amides, hydrazides and imides by proton coupled electron transfer (PCET) is des

82 avoring one rotamer of the resulting Ni(III)-imide, by locking the phenyl ring in a perpendicular ori

83 low coverages, ordered overlayers of phenyl imide (C(6)H(5)N) form at saturation coverage, indicatin

84 tylimidazolium-bis(tetrafluoromethylsulfonyl)imide (C(8)mimC(1)C(1)N) ionic liquid.

85 hylpyrrolidinium bis(trifluoromethylsulfonyl)imide [C(4)C(1)pyrr][NTf(2)], toward such rapid "on-the-

86 ylpyrolydinium bis (trifluromethyl sulfonyl) imide [C(4)mpyr][NTf(2)].

87 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([C2mim][NTf2]) and N-butyl-N-methyl-pyrrolidinium

88 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([C2mim][NTf2]) is demonstrated using low-cost pla

89 thylimidazolium bis(trifluoromethanesulfonyl)imide ([C2mim][NTf2]).

90 thylimidazolium bis(trifluoromethanesulfonyl)imide ([C4mim][NTf2]) using a surface forces apparatus w

91 4mim][OTf]), and bis(trifluoromethylsulfonyl)imide ([C4mim][Tf2N]) were synthesized via a halide-free

92 butylimidazolium bis(trifluoromethylsulfonyl)imide ([C4MIM][TFSI]) were confined within the hybrid ne

93 thylimidazolium bis(trifluoromethanesulfonyl)imide [C4mim][NTf2], with concentration varied using met

94 yl-3-methylimidazolium bis(trifluorosulfonyl)imide [C4mim][Tf2N]) as extraction solvent.

95 yl-pyrrolidinium bis(trifluoromethylsulfonyl)imide ([C4mpyrr][NTf2]).

96 thylimidazolium bis(trifluoromethylsulfonyl)-imide [C6MIM][Tf2N] as ionic liquid for the detection of

97 ese macrocyclic inhibitors identified a P(3) imide capped analogue 52 that was 20 times more potent t

98 Thus, the introduction of these imide caps improved the cell-based replicon EC(90) by mo

99 rotonated quinoline nitrogen (N(+)-H) and an imide carbonyl (O horizontal lineC).

100 f a strong n->pai* stabilization between the imide carbonyl oxygens and the ortho R group in the plan

101 rogen bonding interaction between one of the imide carbonyls and Cys159.

102 tivity toward the hydrogenation of amide and imide carbonyls at low temperatures in THF-d8.

103 teraction between the quinoline nitrogen and imide carbonyls.

104 Contrary to uranium imide chemistry, traditional and routine synthesis proto

105 2N]) and choline bis(trifluoromethylsulfonyl)imide ([choline][Tf2N]) showed that (1) the specific ene

106 A rare, low-spin Fe(IV) imide complex [(pyrr2py)Fe=NAd] (pyrr2 py(2-) = bis(pyrr

107 t -80 degrees C to yield an inverse sandwich imide complex arising from C-H bond activation of toluen

108 The imide complex is low-spin with temperature-independent p

109 d cleavage to form a Nb(V) horizontal lineNR imide complex, (i)PrN horizontal lineNb((i)PrNPPh2)3Fe-P

110 ronically similar to the previously reported imide complex, [SiP(iPr)(3)]Ru(NAr) (Ar = p-CF(3)C(6)H(4

111 led to the isolation of the formally Ru(III) imide complex, [SiP(iPr)(3)]Ru(NAr) (Ar = p-MeOC(6)H(4),

112 take place for the alkyl-substituted Ni(III)-imide complex.

113 Neutral imide complexes ((R)dmx)Cu(2)(mu(2)-NAr) (R: Mes, (t)Bu;

114 sbauer spectroscopy confirmed that all three imide complexes are in the iron(IV) oxidation state.

115 Three five-coordinate iron(IV) imide complexes have been synthesized and characterized.

116 Anionic molecular imide complexes of aluminium are accessible via a ration

117 N-alkyl substituted bis(imino)pyridine iron imide complexes, ((iPr)PDI)FeNR ((iPr)PDI = 2,6-(2,6-(i)

118 The iron(IV) imide complexes, (Me2IPr)-R2Fe=NAd (R = (neo)Pe (3a), 1-

119 tocols seem less viable for rare-earth metal imide complexes.

120 A novel imide compound (C(16)H(10)ClNO(4)) was synthesized in a

121 As a promising cathode candidate, imide compounds have attracted extensive attention due t

122 The two Ni(III)-imide compounds showed different variable-temperature ma

123 s led to the corresponding phosphinidene and imide compounds.

124 A heterotelechelic poly(norbornene imide) containing two terminal and orthogonal hydrogen-b

125 ter norbornene imide-b-N-methyloxanorbornene imide) copolymers were prepared by pulsed-addition ring-

126 ucture of the bis(imino)pyridine iron N-aryl imide counterparts.

127 nium-nitride moiety to give the U(III)/U(IV) imide cyclometalate complex, [((Me(3)Si)(2)N)(2)(THF)U(m

128 , herein we report the synthesis of perylene imide derivatives endowed with a 1,2-diketone functional

129 leading to interesting highly functionalized imide derivatives.

130 With an imide derived from L-tartaric acid as the starting mater

131 wetted by a 4 m potassium bis(fluorosulfonyl)imide-dimethoxyethane electrolyte (theta(CA) = 0 degrees

132 me functionalities do not bind V, the cyclic imide-dioxime group of the adsorbent forms a peculiar no

133 al seawater confirms V binding solely by the imide-dioximes.

134 (proteasome inhibitors and immunomodulatory imide drugs).

135 h proteasome inhibitors and immunomodulatory imide drugs, time from diagnosis to ASCT, and cytogeneti

136 owever, the redox active site utilization of imide electrodes remains challenging for them to fulfill

137 electron donor and a C-terminal perylene bis-imide electron acceptor.

138 thylimidazolium bis(trifluoromethanesulfonyl)imide (EMI-TFSI) electrolytes.

139 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([EMI][TFSI]).

140 ethylimidazolium bis(trifluoromethylsulfonyl)imide (EmimNTf2).

141 thylimidazolium bis(trifluoromethanesulfonyl)imide (EMMIM TFSI), is investigated in situ under applie

142 show that alane binding greatly affects the imide-enamide equilibria and that alane complexation mig

143 ee alkyl-substituted bis(imino)pyridine iron imides established essentially planar compounds with rel

144 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([FcEMIM][TFSI]), has been investigated on both ma

145 The absorption of the chlorin-(iso)imides fills the spectral window between that of analogo

146 DGs than pyridine-containing ones or cyclic imides for this type of C-H bond functionalization.

147 nolase bound to both SF2312 and its oxidized imide-form.

148 w epimerization of the citric acid moiety or imide formation influence its function as a siderophore.

149 SBimide is an imide analogous to the imide forms of other citric acid siderophores that are o

150 alpha,beta-Unsaturated imides, formylated at the nitrogen atom, comprise a new

151 ns and high-concentration bis(fluorosulfonyl)imide (FSI) anions, with sodium bis(trifluoromethanesulf

152 ng materials providing access to any desired imide functionality.

153 ymer solar cells (all-PSCs) are dominated by imide-functionalized polymers, which typically show medi

154 lkynyl-imides (ynimides) generate N,N-di-Boc imide-functionalized triazole and isoxazole heterocycles

155 ning 0 to 4 methylenic units (m) between the imide group and the dendron, (3,4,5)12G1-m-PBI, is repor

156 o the lower-lying HOMO induced by the higher imide group density.

157 based on dicyanobenzothiadiazole without an imide group is reported.

158 relative to one another by attachment of the imide group of each PDI to the 4- and 5-positions of a x

159 Furthermore, the distal imide group of one PDI is linked to the para-position of

160 om planarity with dihedral angles around the imide group reaching ca. -150.3 degrees (C1-N1-C2-O21 =

161 ent conversion of the diester groups into an imide group resulted in novel PBIs (e.g., compound 14) w

162 ed to the electron-withdrawing effect of the imide groups and the kinetic blocking of the most reacti

163 semifluorinated dendron was attached to the imide groups of the NBI via one, two, and three (m = 1,

164 that contain either one or two bis(sulfonyl)imide groups on the side-chain in addition to a terminal

165 plex core coated with bacterial membrane and imide groups to enhance antigen retrieval is developed.

166 Here, a PBI functionalized at its imide groups with a second generation self-assembling de

167 d but also through-space conjugation between imide groups, which leads to distinct optical and electr

168 -1-C2 to PBI-1-C5) between the amide and PBI imide groups.

169 cular hydrogen bonding between the amide and imide groups.

170 imum length (C4 chain) between the amide and imide groups.

171 the steric hindrance associated with typical imide groups.

172 thylimidazolium bis(trifluoromethanesulfonyl)imide has been investigated using transient cyclic volta

173 or the synthesis of a variety of substituted imides has been developed.

174 ne-catalyzed [4+1] cycloadditions of allenyl imides have been discovered using various N-based substr

175 tonated betaine bis(trifluoromethyl sulfonyl)imide ([Hbet][Tf2N]) and choline bis(trifluoromethylsulf

176 otonated betaine bis(trifluoromethylsulfonyl)imide ([Hbet][Tf2N]) was obtained by heating and maintai

177 rocene, such as bis(trifluoromethanesulfonyl)imide, hexafluorophosphate, perchlorate, tetrafluorobora

178 yr(im)idine N functionality and preorganized imide hinge (the "CO...CO" twist) together with the inhe

179 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([hmim][Tf(2)N]), was used as aqueous phase substi

180 membranes in single and multiple poly(amide-imide) hollow fibers, with H2/C3H8 and C3H6/C3H8 separat

181 Poly(tert-butyl ester norbornene imide) homopolymers and poly(tert-butyl ester norbornene

182 omplex 4 also reacts with H(2) to produce an imide hydride U(III)/U(IV) complex, [{((Me(3)Si)(2)N)(2)

183 lkanes with simple amides, sulfonamides, and imides (i.e., benzamides, tosylamides, carbamates, and p

184 ess support a mechanism in which a transient imide (imidyl) aziridinates the diimine, which subsequen

185 hylimidazolium bis(trifluoromethane-sulfonyl)imide, improves stability of the antibody.

186 With 4 M lithium bis(fluorosulfonyl)imide in 1,2-dimethoxyethane as the electrolyte, a lithi

187 hylimidazolium bis((trifluoromethyl)sulfonyl)imide in an operating EDLC with electrodes composed of p

188 ethylimidazolium bis(trifluoromethylsulfonly)imide in the poly(ether sulfone) membrane with average p

189 rocene carboxylic acids, isocyanates provide imides in good yields.

190 acyclic 1,2-diketones to deliver amides and imides in high yields.

191 ns of terminal alkynes to 1,2,4-triazolium N-imides in the presence of base and Cu(I) afford pyrazolo

192 utyl imidazolium bis(trifluoromethylsulfonyl)imide, in a mixture of tetrahydrofuran and water under o

193 n provide a thermodynamic preference for the imide intermediate.

194 line and azobenzene via a putative zirconium-imide intermediate.

195 hylpyrrolidinium bis(trifluoromethylsulfonyl)imide ionic liquid (BMPyrTFSI).

196 D magnetic measurements on the isomeric iron imides, ((iPr)PDI)FeN(1)Ad and ((iPr)PDI)FeN(2)Ad, estab

197 and 2,1,3-benzothiadiazole-5,6-dicarboxylic imide is reported.

198 Nitrene transfer from core imides is negligible.

199 coupling of diols and amines to form cyclic imides is reported.

200 The products include imide, isocyanide, vinyl, alkyl, azide, triazenido, benz

201 The potassium salt of polyheptazine imide (K-PHI) is a promising photocatalyst for various c

202 scalable protocols for the union of amides, imides, ketones, and oxindoles using soluble copper(II)

203 igated, and the potassium bis(fluorosulfonyl)imide (KFSI) salt-based carbonate electrolyte is versati

204 rst time that a potassium bis(fluoroslufonyl)imide (KFSI)-dimethoxyethane (DME) electrolyte forms a u

205 The crystal structure of the ternary imide Li 2Ca(NH) 2 has been determined using neutron pow

206 sing the new salt lithium bis(fluorosulfonyl)imide (LiFSI) with respect to LiPF6.

207 w the bonding is distinctly different on the imide ligand between the two spin states.

208 nt nucleophilicity of N2-derived nitride and imide ligands within a trimetallic iron system and point

209 e naphthalene diimide units, a robust cyclic imide linkage, high surface area, and well-defined acces

210 unts of lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) to understand the impact of a salt on the

211 on nanocrystal-seeded surfaces of poly(amide-imide) macroporous hollow fibers (right).

212 reactivity of the beta-diketiminato Ni(III)-imide [Me(3)NN]Ni horizontal lineNAd (1), which undergoe

213 ion of 1 with indane along with the dinickel imide {[Me(3)NN]Ni}(2)(mu-NAd) (5).

214 The nonplanarity of the imide moiety and the related conformational properties a

215 roved most useful in stabilizing the Ni(III)-imide moiety was the bulky 2,6-dimesitylphenyl.

216 Furthermore, imide N-substituent variation has negligible impact on p

217 reactive metabolite N-acetyl-p-benzoquinone-imide (NAPQI) (r= 0.739;P= 0.058).

218 ns, with sodium bis(trifluoromethanesulfonyl)imide (NaTFSI) as a key additive are reported.

219 4)), diazene (N(2)H(2)), nitride (N(3-)) and imide (NH(2-)), may be involved.

220 Iron imide/nitrene intermediates [Fe(qpy)(NR)(X)](n+) (CX, X

221 ncluding alkyl, aryl, arene, carbene, amide, imide, nitride, alkoxide, aryloxide, and oxo compounds,

222 ows the attachment of the donor group to one imide nitrogen and a solubilizing swallowtail, normally

223 connected to the PDI with the nitroxide and imide nitrogen atoms either para (1) or meta (3) to one

224 y donor (DAB) attached to either one or both imide nitrogen atoms of a perylene-3,4:9,10-bis(dicarbox

225 or hydrogen atoms (H-tpPDI) attached to its imide nitrogen atoms.

226 unpaired electron is mostly localized on the imide nitrogen for the Ni(III) complexes.

227 V(2+) = 4,4'-bipyridinium and NI = naphthyl imide, NIV) are described.

228 (PF(6)(-)) and bis[(trifluoromethyl)sulfonyl]imide (NTf(2)(-)) anions, FAP-based ILs are significantl

229 Bis (trifluoromethylsulfonyl)imide (NTf2) anion of ionic liquid electrolyte was selec

230 bserved when the bis(trifluoromethylsulfonyl)imide (NTf2) anion replaced the PF6(-) anion, leading to

231 s containing the bis(trifluoromethylsulfonyl)imide [NTf2] anion.

232 ded Dieckmann cyclization with a concomitant imide opening, Horner-Wadsworth-Emmons olefination, and

233 ty and the latter with an NCO-alkyl residue (imide or carbamate).

234 mine units are formally in amine, amide, and imide oxidation states.

235 iethyl(methyl)phosphonium bis(fluorosulfonyl)imide (P1222FSI) samples with different thermal history

236 decylphosphonium bis(trifluoromethylsulfonyl)imide ([P14,6,6,6][NTf2]) and the polymer poly(hexyl met

237 e oxide/lithium bis(trifluoromethanesulfonyl)imide (PEO/LiTFSI) that can be used as a safe solid poly

238 e the cis-trans isomerization of the proline imide peptide bond in many cell signaling pathways.

239 that has a 3,5-dialkoxy substitution on the imide phenyl groups (CBI-35CH), leading to "molecular po

240 photocatalytic properties of poly(heptazine imide) (PHI), the microswimmers are activated by both vi

241 ylimidazolium) bis[(trifluoromethyl)sulfonyl]imide [poly(VHIM-NTf(2))] and poly(1-vinyl-3-hexylimidaz

242 ontain hydrogen-bonding amide side groups in imide position and chlorine, methoxy, or methylthio subs

243 he strategically important and less explored imide position of 1,8-naphthalimides.

244 bipyridine groups covalently attached at the imide positions quantitatively yields an Fe4(PBI)6 tetra

245 olecules are directly linked at one of their imide positions, reveals ultrafast formation of the (T(1

246 th 1-phth2 to form the corresponding N-alkyl imide product.

247 A series of imide products are synthesized, and the synthesis of a p

248 flic acid promotes the formation of aromatic imide products in fair to good yields.

249 s of the layered bulk material poly(triazine imide), PTI, followed by one-step liquid exfoliation in

250 o-OMeTAD/lithium bis(trifluoromethylsulfonyl)imide/pyridinium additives as hole transport layer were

251 Pyridinium bis(trifluoromethylsulfonyl)imide (PyTFSI)-templated syntheses of 2,6-pyridyl crypta

252 All imide (RCH(2)CH horizontal lineN(-)) and enamide (RCH(-)

253 ollowing the same one-pot procedure, amidine imides react with the sulfur ylides to provide imidazoli

254 erivatives with various substitutions at the imide region, and several were identified as the most pr

255 s a hexaazatriphenylene "platform" and three imide residues on its concave side carrying flexible alk

256 Imides resist oxidation and promote remote functionaliza

257 thylimidazolium bis(trifluoromethanesulfonyl)imide, respectively.

258 tuted mellitic triimides via dehydration and imide ring closure.

259 Chlorins bearing a six-membered imide ring spanning positions 13-15, commonly referred t

260 Additions of lactams, imides, (S)-4-benzyl-1,3-oxazolidin-2-one, 2-pyridone, p

261 solvents and the lithium bis(fluorosulfonyl)imide salt enables the high-rate cycling of a lithium me

262 oxylic acids provides, in one step, N-formyl imides (see, for example, 8 + 19 --> 21).

263 s such as SNAP receptor [soluble N-ethylmale-imide-sensitive factor-attachment protein receptor (SNAR

264 nt here our first results in this new cyclic-imide series.

265 neglycol ether chain, and aryl group) at the imide sites as well as at the bay regions are described

266 from 4H-pyrido[1,3]oxazin-4-one precursors (imide sodium salts) was developed and led to the desired

267 of a bimolecular coupling mechanism of metal imide species, as shown in the related [SiP(iPr)(3)]Fe s

268 other related amino-substituted perylene bis-imide species.

269 This material has a polytriazine imide structure with Cl(-) ions contained within C12N12

270 le host wider than the corresponding urea or imide structures, and longer alkanes can be accommodated

271 ring ruthenacycle intermediates, the cyclic imides studied herein enabled the hydroxylation of the C

272 est as it provides access to unsymmetrically imide-substituted 1,7-dibromoperylene derivatives, which

273 A new family of low-coordinate nickel imides supported by 1,2-bis(di-tert-butylphosphino)ethan

274 and DNA binding properties of a bis-naphthyl imide tetracationic diviologen compound NI(CH2)3V(2+)(CH

275 dazolium (C2mim) bis(trifluoromethylsulfonyl)imide (Tf2N) and its mixtures with carbon dioxide in ord

276 s en-abled by a bis(trifluoromethanesulfonyl)imide (TFSI-) anion-based room temperature ionic liquid

277 th Tyr-1771 of Na(V)1.2 and a polar amide or imide that interacts with the aromatic ring of Phe-1764

278 on to accessing a wide variety of alpha-keto-imides, the RuO2-NaIO4 protocol provides a novel entry t

279 iamine and zinc bis(trifluoromethanesulfonyl)imide, this ketone formed a new Zn(4) L(4) tetrahedron 1

280 col involving ethanethiolate exchange of the imide to the corresponding thioester, followed by a stan

281 ytic aldol additions of alpha-isothiocyanato imides to aldehydes are reported.

282 s of the glucosamine units were converted to imides to prevent formation of unwanted imidate byproduc

283 ic Mannich additions of alpha-isothiocyanato imides to sulfonyl imines are reported.

284 lytetrafluoroethylene (Teflon) and polyamide-imide (Torlon), discharge when the like-charged beads ar

285 shed a three-coordinate, diamagnetic Co(III) imide ((Tr)L)Co(NAd) as confirmed by single-crystal X-ra

286 , [n]HDI-OMe (n = 5, 6, and 7), in which two imide units are connected via an [n]helicene skeleton.

287 for prototypical organic azides and iodonium imides used in organic synthesis.

288 A de novo preparation of alpha-keto-imides via ynamide oxidation is described.

289 ic addition of PhSCF(2)SiMe(3) (1) to chiral imides was achieved in satisfactory yields to provide mi

290 addition, NFSI (N-fluorobis(phenylsulfonyl)-imide) was explored as an amidating reagent for C8-amida

291 imethylammonium bis(trifluoromethanesulfonyl)imide, was synthesized and characterized by (1)H NMR, (1

292 Using TSE, naphthalic imides were obtained quantitatively without the need for

293 Tryptamine- and phenethylamine-derived imides were selectively monotrifluoromethylated using CF

294 -bonding receptors along the poly(norbornene imide) were synthesized either also via ROMP by terminat

295 thylimidazolium bis(trifluoromethanesulfonyl)imide) were used.

296 arboxylate leads to an intermediate carbonyl imide, which can react with a variety of amines to affor

297 intermediates in the reactions of amides and imides with haloarenes catalyzed by copper complexes con

298 A number of imides with various substitutions, ring sizes, bicyclic

299 as a function of the R-group attached to the imide, with alkyl groups leading to low-spin diamagnetic

300 ocol allows direct C2 arylation of azolium N-imides without the use of specialized reagents together

301 ective [3 + 2] cycloadditions of the alkynyl-imides (ynimides) generate N,N-di-Boc imide-functionaliz