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1 , and N(Tf)(2) = bis(trifluoromethylsulfonyl)imide).
2 d carbonylation and ring closure to form the imide.
3  chlorin-isoimide in addition to the chlorin-imide.
4 a hydrogen storage mechanism for the ternary imide.
5 mpact on the hydrogenation properties of the imide.
6 ment of regioselectively reduced N-homoallyl imides.
7  aldehydes, ketones, esters, carbamates, and imides.
8  possibility to successfully ionize PAHs and imides.
9  of the bis(imino)pyridine alkyl-substituted imides.
10 e efficient access to a variety of hydrazino imides.
11 alcohols to afford the corresponding bis-SES imides.
12                                       Nickel-imide 1 competes with the nickel-amide HAA product [Me(3
13 H by 1 to give R(*), which may add to either imide 1 or amide 2, each featuring significant N-based r
14 magnetically coupled to an imidyl radical (S(imide) = 1/2) and a closed-shell, dianionic bis(imino)py
15 he nitrogen differentially protected enamide imide 12.
16 ether adduct of an asymmetric niobium(V) bis(imide) 2.OEt2 containing the monoazabutadiene (MAD) liga
17 c(Me){NHB(NAr'CH)2} (18) generated transient imide 25 via rate-determining, first-order methane elimi
18 ,N'-4,4'-biphenylene(bis(triphenyl)phosphine imide) (3) forms radical cationic and a dicationic speci
19 M a trans 2-octenoylated, citrate-containing imide 6 was nearly 5-fold more effective in stimulating
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 ne product or reversibly form an aziridinium imide (AI) intermediate that does not participate in the
24 ononitrile are much more stable than lithium imides, alane binding dramatically reduces the enamide p
25 formation of the bis(imino)pyridine vanadium imide amide compounds, ((iPr)BPDI)V(NHAr)NAr, were obser
26                                SBimide is an imide analogous to the imide forms of other citric acid
27 rin a, 13(1)/15(1)-N-alkyl isoimide, and the imide analogues were found to be more stable with a sign
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 is of new organic materials based on arylene imide and bis(imide) dyes, such as perylene-3,4:9,10-bis
31 ng by a regioselective reduction of a chiral imide and cyclization with trifluoromethanesulfonic acid
32 xyuridine without the protection at the N(3)-imide and provides a facile and general access to versat
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 is of 1,4-benzoxazinones from o-benzoquinone imides and ketene enolates is reported.
38 oxyethane, TFSI=bis(trifluoromethanesulfonyl)imide) and realize the best cycling stability among all
39 pected bicyclo[3.2.1]octane (tropane) ether, imide, and amine derivatives but also to unexpected bicy
40 e performed on model compounds of the amide, imide, and cyclic 1,2- and 1,3-species to better underst
41 e utility of this method to generate amides, imides, and carbamates is illustrated by a one-pot synth
42 both aryl- and alkyl-substituted nickel(III)-imides, and examples of both types have been isolated an
43  including alkenes, alkynes, esters, amines, imides, and O-, S-, and N-heterocycles.
44 alently attached to a 4-aminonaphthalene-1,8-imide (ANI) chromophore and a naphthalene-1,8:4,5-bis(di
45 s found that the bis(trifluoromethylsulfonyl)imide anion has the greatest affinity for CO2, while the
46 (2)-2,6-Me(2)-4-Bu(t))(2)), afforded the red imide Ar'GaNAr(#) (2).
47  growth process afforded surface-bound oligo-imide architectures composed of alternating components w
48  (14,15)N ENDOR measurements of the bridging imide are consistent with an allyl radical molecular orb
49 tion/intramolecular cyclization of azolium N-imides are reported.
50 iquids (IL) with bis(trifluoromethylsulfonyl)imide as counterion for lubrication.
51 Reactions involving the olefinic bond of the imide as well as its carbonyl groups are observed and an
52 he discovery of tert-leucinol derived cyclic imides as a potent series of novel P3 capping groups.
53 e was obtained, whereas the use of amines or imides as nucleophile afforded a mixture of the two stru
54 ld synthetic approach to access a variety of imides as well as amides in high yields.
55  of the isoaspartate (IsoAsp) and the cyclic imide (Asu) variants of these MAbs.
56 he protection of the NH group of a series of imides, azinones (including AZT), inosines, and cyclic s
57 olymers and poly(tert-butyl ester norbornene imide-b-N-methyloxanorbornene imide) copolymers were pre
58 thylimidazolium bis(trifluoromethanesulfonyl)imide, background subtraction is necessary at a macrodis
59  provides a facile entry into a new class of imide-based "3 + 3" macrocyclic trimer (trezimide), toge
60 capacity to capture low-concentration CO2 by imide-based ionic liquids.
61 Although it shares a binding site with other imide-based natural product translation inhibitors, CL e
62 nolates to alpha,beta-unsaturated esters and imides bearing adjacent stereocenters (X, Y = H, Me, OR)
63                             The arylation of imides bearing the Evans auxiliary proceeded with select
64 ylene-bis(2,6-dimethylaniline)) gave the bis(imide) bearing a terminal amine.
65 for barbiturate extraction over other cyclic imides becomes better in the presence of barbiturate rec
66 hylimidazolium bis(trifluoromethanesulfonyl)-imide, BMI(Tf2N), has been developed and characterized f
67 ethylimidazolium bis(trifluoromethylsulfonyl)imide (BMIm-TFSI), and some combination of ferrocene (Fc
68 ethylimidazolium bis(trifluoromethylsulfonyl)imide (BmimNTf2) were investigated with two-dimensional
69 hylpyrrolidinium bis(trifluoromethylsulfonyl)imide (BMP TFSI) and dimethylformamide.
70 ylpyrrolidinium-bis(trifluoromethanesulfonyl)imide (BMP-TFSI) IL is beneficial for glucose detection,
71 hylpyrrolidinium bis(trifluoromethylsulfonyl)imide ([Bmpyr](+)[NTf2](-)).
72 omerization about a highly conserved Trp-Pro imide bond in a region of the TAD that is required for n
73             Isomerization of a single prolyl imide bond in this domain is responsible for simultaneou
74                                          The imide bond is twisted, and the O horizontal lineC-N-C(O)
75                            The measured Fe-N(imide) bond distance (1.768(2) A) is the longest reporte
76  planar compounds with relatively short Fe-N(imide) bond lengths and two-electron reduction of the re
77  temperatures via rotation about a C(aryl)-N(imide) bond of a carboxylic acid monomer.
78 of restricted rotation around that C(aryl)-N(imide) bond, which locks the carboxylic acid recognition
79  amines on proteins to yield stable amide or imide bonds.
80 dral oligomeric silsesquioxanes and aromatic imide bridges.
81 olium)dodecane bis[(trifluoromethyl)sulfonyl]imide bromotrichloroferrate(III) ([(C16BnIM)2C12(2+)][NT
82                                  Bithiophene imide (BTI) and benzodithiophene (BDT) copolymers are sy
83 tion for the desymmetrization of meso-cyclic imides by hydrogenation with 8-K are also described here
84 pentadienyl) titanium amides, hydrazides and imides by proton coupled electron transfer (PCET) is des
85 avoring one rotamer of the resulting Ni(III)-imide, by locking the phenyl ring in a perpendicular ori
86 resulting from restricted rotation about the imide C-N bond; the 13C NMR spectra and stereochemistry
87  low coverages, ordered overlayers of phenyl imide (C(6)H(5)N) form at saturation coverage, indicatin
88 tylimidazolium-bis(tetrafluoromethylsulfonyl)imide (C(8)mimC(1)C(1)N) ionic liquid.
89 ylpyrolydinium bis (trifluromethyl sulfonyl) imide [C(4)mpyr][NTf(2)].
90 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([C2mim][NTf2]) and N-butyl-N-methyl-pyrrolidinium
91 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([C2mim][NTf2]) is demonstrated using low-cost pla
92 thylimidazolium bis(trifluoromethanesulfonyl)imide ([C2mim][NTf2]).
93 hylimidazolium bis[(trifluoromethyl)sulfonyl]imide (C4mim+Tf2N(-)), rather than the hydrated, neutral
94 thylimidazolium bis(trifluoromethanesulfonyl)imide ([C4mim][NTf2]) using a surface forces apparatus w
95 4mim][OTf]), and bis(trifluoromethylsulfonyl)imide ([C4mim][Tf2N]) were synthesized via a halide-free
96 butylimidazolium bis(trifluoromethylsulfonyl)imide ([C4MIM][TFSI]) were confined within the hybrid ne
97 thylimidazolium bis(trifluoromethanesulfonyl)imide [C4mim][NTf2], with concentration varied using met
98 yl-3-methylimidazolium bis(trifluorosulfonyl)imide [C4mim][Tf2N]) as extraction solvent.
99 yl-pyrrolidinium bis(trifluoromethylsulfonyl)imide ([C4mpyrr][NTf2]).
100 thylimidazolium bis(trifluoromethylsulfonyl)-imide [C6MIM][Tf2N] as ionic liquid for the detection of
101                                        These imides can be selectively cleaved to the mono-SES-protec
102 ese macrocyclic inhibitors identified a P(3) imide capped analogue 52 that was 20 times more potent t
103              Thus, the introduction of these imide caps improved the cell-based replicon EC(90) by mo
104 rotonated quinoline nitrogen (N(+)-H) and an imide carbonyl (O horizontal lineC).
105 rogen bonding interaction between one of the imide carbonyls and Cys159.
106 tivity toward the hydrogenation of amide and imide carbonyls at low temperatures in THF-d8.
107 teraction between the quinoline nitrogen and imide carbonyls.
108 2N]) and choline bis(trifluoromethylsulfonyl)imide ([choline][Tf2N]) showed that (1) the specific ene
109 m thick) of either plain poly(imide) or poly(imide) coated with amorphous aluminum oxide (AAO), amorp
110                      A rare, low-spin Fe(IV) imide complex [(pyrr2py)Fe=NAd] (pyrr2 py(2-) = bis(pyrr
111                                          The imide complex is low-spin with temperature-independent p
112                              The diamagnetic imide complex {[PhBP(3)]Fe(II)(triple bond)N(1-Ad)}{(n)(
113 d cleavage to form a Nb(V) horizontal lineNR imide complex, (i)PrN horizontal lineNb((i)PrNPPh2)3Fe-P
114 ronically similar to the previously reported imide complex, [SiP(iPr)(3)]Ru(NAr) (Ar = p-CF(3)C(6)H(4
115 led to the isolation of the formally Ru(III) imide complex, [SiP(iPr)(3)]Ru(NAr) (Ar = p-MeOC(6)H(4),
116 take place for the alkyl-substituted Ni(III)-imide complex.
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                                      A novel imide compound (C(16)H(10)ClNO(4)) was synthesized in a
120                              The two Ni(III)-imide compounds showed different variable-temperature ma
121 s led to the corresponding phosphinidene and imide compounds.
122           A heterotelechelic poly(norbornene imide) containing two terminal and orthogonal hydrogen-b
123 ter norbornene imide-b-N-methyloxanorbornene imide) copolymers were prepared by pulsed-addition ring-
124 ucture of the bis(imino)pyridine iron N-aryl imide counterparts.
125 A novel concomitant enamine formation and an imide cyclization afforded the nitrogen differentially p
126 id-hydrolyzed product of helioxanthin cyclic imide derivative 9, was found to exhibit broad-spectrum
127 ction of 8 with N(3)Ar' ' afforded the amido-imide derivative Ar' 'NGaN(SiMe(3))Ar' ' (9), a gallium
128 , herein we report the synthesis of perylene imide derivatives endowed with a 1,2-diketone functional
129                    Two linear and two cyclic imide derivatives were generated and evaluated for growt
130                                      With an imide derived from L-tartaric acid as the starting mater
131 me functionalities do not bind V, the cyclic imide-dioxime group of the adsorbent forms a peculiar no
132 al seawater confirms V binding solely by the imide-dioximes.
133 h proteasome inhibitors and immunomodulatory imide drugs, time from diagnosis to ASCT, and cytogeneti
134 sformation between lithium amide and lithium imide during hydrogen cycling in the important Li-N-H hy
135 nic materials based on arylene imide and bis(imide) dyes, such as perylene-3,4:9,10-bis(dicarboximide
136 electron donor and a C-terminal perylene bis-imide electron acceptor.
137 thylimidazolium bis(trifluoromethanesulfonyl)imide (EMI-TFSI) electrolytes.
138 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([EMI][TFSI]).
139 ethylimidazolium bis(trifluoromethylsulfonyl)imide (EmimNTf2).
140 thylimidazolium bis(trifluoromethanesulfonyl)imide (EMMIM TFSI), is investigated in situ under applie
141  show that alane binding greatly affects the imide-enamide equilibria and that alane complexation mig
142 oieties were obtained by Evans oxazolidinone imide enolate alkylation and hydrazination/cyclization,
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 w epimerization of the citric acid moiety or imide formation influence its function as a siderophore.
147 c methods were developed to overcome issues (imide formation) encountered in earlier syntheses.
148 can be grown in a stepwise fashion using the imide-forming reaction.
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 ng materials providing access to any desired imide functionality.
152 ning 0 to 4 methylenic units (m) between the imide group and the dendron, (3,4,5)12G1-m-PBI, is repor
153 o the lower-lying HOMO induced by the higher imide group density.
154 relative to one another by attachment of the imide group of each PDI to the 4- and 5-positions of a x
155                      Furthermore, the distal imide group of one PDI is linked to the para-position of
156 om planarity with dihedral angles around the imide group reaching ca. -150.3 degrees (C1-N1-C2-O21 =
157 ed to the electron-withdrawing effect of the imide groups and the kinetic blocking of the most reacti
158  semifluorinated dendron was attached to the imide groups of the NBI via one, two, and three (m = 1,
159            Here, a PBI functionalized at its imide groups with a second generation self-assembling de
160 -1-C2 to PBI-1-C5) between the amide and PBI imide groups.
161 cular hydrogen bonding between the amide and imide groups.
162 imum length (C4 chain) between the amide and imide groups.
163 thylimidazolium bis(trifluoromethanesulfonyl)imide has been investigated using transient cyclic volta
164        The aromatic linker between phosphine imides has also been modified.
165 ntil now, the synthesis of N-arylated cyclic imides having six-membered rings was restricted largely
166 tonated betaine bis(trifluoromethyl sulfonyl)imide ([Hbet][Tf2N]) and choline bis(trifluoromethylsulf
167 otonated betaine bis(trifluoromethylsulfonyl)imide ([Hbet][Tf2N]) was obtained by heating and maintai
168 rocene, such as bis(trifluoromethanesulfonyl)imide, hexafluorophosphate, perchlorate, tetrafluorobora
169 yr(im)idine N functionality and preorganized imide hinge (the "CO...CO" twist) together with the inhe
170 ethylimidazolium bis(trifluoromethylsulfonyl)imide ([hmim][Tf(2)N]), was used as aqueous phase substi
171  membranes in single and multiple poly(amide-imide) hollow fibers, with H2/C3H8 and C3H6/C3H8 separat
172             Poly(tert-butyl ester norbornene imide) homopolymers and poly(tert-butyl ester norbornene
173 lkanes with simple amides, sulfonamides, and imides (i.e., benzamides, tosylamides, carbamates, and p
174  (229 nm) ultraviolet resonance Raman (UVRR) imide II band reveals a common structural feature for ge
175 ess support a mechanism in which a transient imide (imidyl) aziridinates the diimine, which subsequen
176 hylimidazolium bis(trifluoromethane-sulfonyl)imide, improves stability of the antibody.
177          With 4 M lithium bis(fluorosulfonyl)imide in 1,2-dimethoxyethane as the electrolyte, a lithi
178 hylimidazolium bis((trifluoromethyl)sulfonyl)imide in an operating EDLC with electrodes composed of p
179 ethylimidazolium bis(trifluoromethylsulfonly)imide in the poly(ether sulfone) membrane with average p
180 rocene carboxylic acids, isocyanates provide imides in good yields.
181 ns of terminal alkynes to 1,2,4-triazolium N-imides in the presence of base and Cu(I) afford pyrazolo
182 utyl imidazolium bis(trifluoromethylsulfonyl)imide, in a mixture of tetrahydrofuran and water under o
183 ersion of the compound nor the unsubstituted imide inhibit substrate cleavage, which is consistent wi
184 n provide a thermodynamic preference for the imide intermediate.
185 line and azobenzene via a putative zirconium-imide intermediate.
186 hylpyrrolidinium bis(trifluoromethylsulfonyl)imide ionic liquid (BMPyrTFSI).
187 D magnetic measurements on the isomeric iron imides, ((iPr)PDI)FeN(1)Ad and ((iPr)PDI)FeN(2)Ad, estab
188 der reaction of cyclopentadiene and acrylate imide is presented.
189  and 2,1,3-benzothiadiazole-5,6-dicarboxylic imide is reported.
190                   Nitrene transfer from core imides is negligible.
191 ion of trimethylsilyl enolates of esters and imides is reported.
192  coupling of diols and amines to form cyclic imides is reported.
193                         The products include imide, isocyanide, vinyl, alkyl, azide, triazenido, benz
194  scalable protocols for the union of amides, imides, ketones, and oxindoles using soluble copper(II)
195 rst time that a potassium bis(fluoroslufonyl)imide (KFSI)-dimethoxyethane (DME) electrolyte forms a u
196         The crystal structure of the ternary imide Li 2Ca(NH) 2 has been determined using neutron pow
197 sing the new salt lithium bis(fluorosulfonyl)imide (LiFSI) with respect to LiPF6.
198 nt nucleophilicity of N2-derived nitride and imide ligands within a trimetallic iron system and point
199                                    The other imide link was to a donor group (pyrene, ferrocene, tetr
200 es that contain bridged nitride and terminal imide linkages, and exhibit singlet ground-state electro
201 long wire, (190 ps)(-1) and 81%; perylene-(N-imide)-linked long wire, (175 ps)(-1) and 86%.
202  energy transfer are as follows: perylene-(N-imide)-linked short wire, (33 ps)(-1) and >99%; perylene
203 on nanocrystal-seeded surfaces of poly(amide-imide) macroporous hollow fibers (right).
204  reactivity of the beta-diketiminato Ni(III)-imide [Me(3)NN]Ni horizontal lineNAd (1), which undergoe
205 ion of 1 with indane along with the dinickel imide {[Me(3)NN]Ni}(2)(mu-NAd) (5).
206                      The nonplanarity of the imide moiety and the related conformational properties a
207 roved most useful in stabilizing the Ni(III)-imide moiety was the bulky 2,6-dimesitylphenyl.
208 tructural elements were identified (e.g., an imide motif or 2-octenoyl side chain), whose presence st
209 ional studies on the monomer showed that the imide N-H was a weak hydrogen bond donor, rationalizing
210                                 Furthermore, imide N-substituent variation has negligible impact on p
211  reactive metabolite N-acetyl-p-benzoquinone-imide (NAPQI) (r= 0.739;P= 0.058).
212 s identified the dichlorophenyl ring and the imide NH as important pharmacophores.
213 4)), diazene (N(2)H(2)), nitride (N(3-)) and imide (NH(2-)), may be involved.
214                                         Iron imide/nitrene intermediates [Fe(qpy)(NR)(X)](n+) (CX, X
215 ncluding alkyl, aryl, arene, carbene, amide, imide, nitride, alkoxide, aryloxide, and oxo compounds,
216 functional groups, including esters, amides, imides, nitriles, and heterocycles.
217 ows the attachment of the donor group to one imide nitrogen and a solubilizing swallowtail, normally
218 action of a sulfate ion oxygen atom with the imide nitrogen atom.
219  connected to the PDI with the nitroxide and imide nitrogen atoms either para (1) or meta (3) to one
220 y donor (DAB) attached to either one or both imide nitrogen atoms of a perylene-3,4:9,10-bis(dicarbox
221 unpaired electron is mostly localized on the imide nitrogen for the Ni(III) complexes.
222 ing uncommon sugars and substitutions on the imide nitrogen have been synthesized.
223                                          One imide nitrogen was attached to a "swallowtail" lipid (a
224  V(2+) = 4,4'-bipyridinium and NI = naphthyl imide, NIV) are described.
225 (PF(6)(-)) and bis[(trifluoromethyl)sulfonyl]imide (NTf(2)(-)) anions, FAP-based ILs are significantl
226                 Bis (trifluoromethylsulfonyl)imide (NTf2) anion of ionic liquid electrolyte was selec
227 bserved when the bis(trifluoromethylsulfonyl)imide (NTf2) anion replaced the PF6(-) anion, leading to
228 s containing the bis(trifluoromethylsulfonyl)imide [NTf2] anion.
229 h M. avium subsp. paratuberculosis using the imide of acinetoferrin.
230  from the Rh(II)-catalyzed reaction of diazo imides, on the other hand, undergo successful intramolec
231 ded Dieckmann cyclization with a concomitant imide opening, Horner-Wadsworth-Emmons olefination, and
232 rylene-monoimide dye (linked either at the N-imide or the C9 position); the transmission element cons
233  5 mm; 10-microm thick) of either plain poly(imide) or poly(imide) coated with amorphous aluminum oxi
234       Bacteriochlorins containing anhydride, imide, or isoimide cyclic rings demonstrated a significa
235 l-tropane intermediate with alkoxides, metal imides, or amines was found to lead not only to the expe
236 mine units are formally in amine, amide, and imide oxidation states.
237 iethyl(methyl)phosphonium bis(fluorosulfonyl)imide (P1222FSI) samples with different thermal history
238 decylphosphonium bis(trifluoromethylsulfonyl)imide ([P14,6,6,6][NTf2]) and the polymer poly(hexyl met
239 e the cis-trans isomerization of the proline imide peptide bond in many cell signaling pathways.
240  that has a 3,5-dialkoxy substitution on the imide phenyl groups (CBI-35CH), leading to "molecular po
241 ylimidazolium) bis[(trifluoromethyl)sulfonyl]imide [poly(VHIM-NTf(2))] and poly(1-vinyl-3-hexylimidaz
242 he strategically important and less explored imide position of 1,8-naphthalimides.
243 bipyridine groups covalently attached at the imide positions quantitatively yields an Fe4(PBI)6 tetra
244 th 1-phth2 to form the corresponding N-alkyl imide product.
245 mophthalimides 2 (R' = H), bearing an acidic imide proton capable of acting as a carboxylic acid bioi
246 s of the layered bulk material poly(triazine imide), PTI, followed by one-step liquid exfoliation in
247 o-OMeTAD/lithium bis(trifluoromethylsulfonyl)imide/pyridinium additives as hole transport layer were
248       Pyridinium bis(trifluoromethylsulfonyl)imide (PyTFSI)-templated syntheses of 2,6-pyridyl crypta
249                                          All imide (RCH(2)CH horizontal lineN(-)) and enamide (RCH(-)
250 erivatives with various substitutions at the imide region, and several were identified as the most pr
251 s a hexaazatriphenylene "platform" and three imide residues on its concave side carrying flexible alk
252                                              Imides resist oxidation and promote remote functionaliza
253 thylimidazolium bis(trifluoromethanesulfonyl)imide, respectively.
254 s much more stable than the isomeric Ga(III) imide RGaNR.
255 tuted mellitic triimides via dehydration and imide ring closure.
256              Chlorins bearing a six-membered imide ring spanning positions 13-15, commonly referred t
257 nzobacteriochlorins containing N-substituted-imide ring system produced enhanced photosensitizing eff
258                     p-Phenylenebis(phosphine imide)s Ar3PNC6H4NPAr3 (1a-d) have two reversible single
259 nd spectroscopic properties of bis(phosphine imide)s have been investigated.
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 nt here our first results in this new cyclic-imide series.
264        Bis(beta-trimethylsilylethanesulfonyl)imide (SES(2)NH) can be easily prepared in 85% yield by
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  the sugar, rather than the modifications in imide structure on the indolocarbazole ring, is a key el
270             This material has a polytriazine imide structure with Cl(-) ions contained within C12N12
271 le host wider than the corresponding urea or imide structures, and longer alkanes can be accommodated
272 est as it provides access to unsymmetrically imide-substituted 1,7-dibromoperylene derivatives, which
273  atom transfer reactions of an oxazolidinone imide substrate, 1, derived from alpha-bromo acetic acid
274        A new family of low-coordinate nickel imides supported by 1,2-bis(di-tert-butylphosphino)ethan
275 cessfully translated to the bacteriopurpurin imide system 19 (lambdamax: 792 nm) and within both seri
276 and DNA binding properties of a bis-naphthyl imide tetracationic diviologen compound NI(CH2)3V(2+)(CH
277 dazolium (C2mim) bis(trifluoromethylsulfonyl)imide (Tf2N) and its mixtures with carbon dioxide in ord
278 s en-abled by a bis(trifluoromethanesulfonyl)imide (TFSI-) anion-based room temperature ionic liquid
279 er electrolyte, bis(trifluoromethanesulfonyl)imide (TFSI-), yielded transistors that showed clear cur
280 th Tyr-1771 of Na(V)1.2 and a polar amide or imide that interacts with the aromatic ring of Phe-1764
281 on to accessing a wide variety of alpha-keto-imides, the RuO2-NaIO4 protocol provides a novel entry t
282 col involving ethanethiolate exchange of the imide to the corresponding thioester, followed by a stan
283 ytic aldol additions of alpha-isothiocyanato imides to aldehydes are reported.
284 ic Mannich additions of alpha-isothiocyanato imides to sulfonyl imines are reported.
285 lytetrafluoroethylene (Teflon) and polyamide-imide (Torlon), discharge when the like-charged beads ar
286                                              Imide-type nucleophiles were found to be directed to the
287 ligomers of porphyrins linked covalently via imide units.
288 for prototypical organic azides and iodonium imides used in organic synthesis.
289          A de novo preparation of alpha-keto-imides via ynamide oxidation is described.
290 ic addition of PhSCF(2)SiMe(3) (1) to chiral imides was achieved in satisfactory yields to provide mi
291  However, a series of N-farnesyl lactams and imides was converted to the desired phosphonates through
292 imethylammonium bis(trifluoromethanesulfonyl)imide, was synthesized and characterized by (1)H NMR, (1
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                                       Cyclic imides within six-membered rings are shown to undergo ef
300 ocol allows direct C2 arylation of azolium N-imides without the use of specialized reagents together

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