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1 nol dialdehyde and an optically active BINOL dialdehyde.
2  activity lost in cytosol treated with NADPH dialdehyde.
3 dase assays was lost on treatment with NADPH dialdehyde.
4 rysene-fused tripyrranes and a chrysopyrrole dialdehyde.
5 pared to the detection limit of the starting dialdehyde.
6  bis(3-indenyl)methane and a dipyrrylmethane dialdehyde.
7 amethoxybenzophenone also afforded a related dialdehyde.
8 reacting it with the appropriate triamine or dialdehyde.
9 nation and polycondensation with an aromatic dialdehyde.
10  methyltransferase inhibitor adenosine-2',3'-dialdehyde.
11  promote selective monofunctionalizations of dialdehydes.
12 idatively ring-opened to afford cyclopentane dialdehydes.
13 ialdehydes similarly reacted to give fulvene dialdehydes.
14 ,12-dialdehyde oxidation product (TBOH-11,12-dialdehyde; 1.0 mg) after irradiation of approximately 1
15  with TFA, "3 + 1" condensation with pyrrole dialdehyde 12 gave the fluoranthoporphyrins 13 in good o
16             The tetrakis (tetrahydrofuranyl) dialdehydes 14 and 19 are accessible by oxidative cleava
17 tion of tripyrrane 11 with acenaphthopyrrole dialdehyde 16 gave the mixed acenaphthofluoranthoporphyr
18 groups to give novel dicarboxylic acid 11 or dialdehyde 16 in practical yields.
19                                              Dialdehyde 16 shows fast self-exchange between two equiv
20 ne, we identified the alpha,beta-unsaturated dialdehyde 2-butene-1,4-dial (BDA) and its chlorinated a
21 ormation the novel one-pot transformation of dialdehyde 24 to pentacyclic unsaturated amine 25.
22                                              Dialdehydes 3 and 16 were comparable on both counts.
23 synthesized in high yield from diamine 4 and dialdehyde 5.
24                                              Dialdehyde 7 has been synthesized, converted into a vari
25  for 24 or 72 h in the presence of adenosine dialdehyde, a potent methyltransferase inhibitor, a subs
26 on we cultured rat PC12 cells with adenosine dialdehyde (AdOx), a methyltransferase inhibitor that pr
27 ral transcription, we utilized adenosine-2,3-dialdehyde (AdOx), an adenosine analog and S-adenosylmet
28 cetylated prior to isolation while the gluco-dialdehyde afforded a mixture of three stereoisomers in
29 ns of an N-methyltripyrrane with a series of dialdehydes afforded a matched set of N-methylporphyrins
30 yrin in 50% yield, while furan and thiophene dialdehydes afforded the corresponding oxa- and thiasapp
31 e-fused dipyrrylmethane with dipyrrylmethane dialdehydes afforded unique dipyrromethene-naphthoporphy
32 TNF-alpha-induced IL-6 production, adenosine dialdehyde, an inhibitor of S-adenosylhomocysteine hydro
33 )- ion centers with appropriate amounts of a dialdehyde and a diamine to facilitate the [n]rotaxane f
34 sized starting from both an achiral biphenol dialdehyde and an optically active BINOL dialdehyde.
35 ation with authentic standards, are crocetin dialdehyde and crocetin, respectively.
36 methane, "3 + 1" condensation with a pyrrole dialdehyde and dehydrogenation of the phlorin intermedia
37 alene 2-boronic acid with 2-bromobenzene-1,3-dialdehyde and requires only three steps.
38 ithium aluminum hydride afforded an unstable dialdehyde and subsequent acid-catalyzed condensation wi
39                 Dehydration to form both the dialdehyde and the monohydrate is both acid- and base-ca
40 e substrate symmetrically to produce a C(14) dialdehyde and two C(13) products, which vary depending
41 the 9,10 (9',10') positions to produce a C14 dialdehyde and two C13 cyclohexones that vary depending
42 d in nitroaldol systems composed of aromatic dialdehydes and aliphatic or aromatic dinitroalkanes.
43               The different behavior between dialdehydes and ketoaldehydes is suggested to be resulti
44 ed by condensation with a series of aromatic dialdehydes and oxidation with DDQ, afforded the tropone
45 e studied the formation and exchange of both dialdehydes and triamines of two different [2 + 3] imine
46  2',3'-dialdehyde derivative of NADPH (NADPH dialdehyde) and neutrophil cytosol.
47 n and reaction of butenedial, a semivolatile dialdehyde, and reduced nitrogen (NH(X)) in bulk solutio
48 aries (CDLs)-each containing two amines, two dialdehydes, and two metal salts-have been found to self
49 DA; 3,4-dihydroxyphenylethanol-elenolic acid dialdehyde), are believed to play a role in the preventi
50 e-containing fulvene gave good yields of the dialdehyde at -78 degrees C or -100 degrees C, but the f
51 valently cross-linked product by utilizing a dialdehyde-based cross-linker, 1.
52 tion of the building blocks benzodithiophene-dialdehyde (BDT) and N,N,N',N'-tetra(4-aminophenyl)benze
53  azatriangulenes (OTPA) and benzodithiophene dialdehydes (BDT), which afforded a new semiconducting C
54 d and nonlabeled building blocks showed full dialdehyde building block exchange over 13 days for open
55 5-Tris(4-aminophenyl)adamantane, with linear dialdehyde building blocks allowed the construction of t
56 ynthesized from simple aromatic triamine and dialdehyde building blocks by dynamic imine chemistry at
57 used tripyrranes were reacted with a pyrrole dialdehyde, but poor yields of chrysoporphyrins were obt
58 synthesized from O-alkylcalixarene mono- and dialdehydes by a two-step conversion to the correspondin
59  nano-composite named Fe(3)O(4)@SiO(2)-NH(2)@dialdehyde cellulose (DAC)@CNT-COOH as an effectual sorb
60                                  A series of dialdehyde compounds were synthesized and reacted with t
61 ns within a knottin monomer and reacted with dialdehyde-containing cross-linkers of different lengths
62 e studied the interactions between the 2',3'-dialdehyde derivative of NADPH (NADPH dialdehyde) and ne
63 ) mice have elevated glyoxalase I (GLO-1), a dialdehyde detoxifying enzyme.
64 vailable di-Boc trifluoromethylhydrazine and dialdehydes, diketones, carbonylnitriles, and ketoesters
65 te is thought to be an aliphatic C5 semi- or dialdehyde, e.g., glutaric dialdehyde (Km = 1 mM).
66    However, the thiophene-containing fulvene dialdehyde failed to give any of the anticipated macrocy
67 clitols, while bis-Wittig olefination of the dialdehyde followed by Grubb's(II)-catalyzed RCM deliver
68  condensation of tripyrranes with monocyclic dialdehydes, followed by an oxidation step.
69                    Allylindation of the same dialdehyde gave rise to lactol 16, a reactivity pattern
70                 However, furan and thiophene dialdehydes gave highly insoluble products that could no
71                Manno- and galacto-configured dialdehydes gave predominantly single inosose stereoisom
72 h pyrrole, furan, thiophene, and selenophene dialdehydes gave tropone-fused porphyrins and related he
73 agent, Acetyl Yellow 9 (AY9), using glutaric dialdehyde (GDI) as a molecular tether.
74 y cross-linking the system with the glutaric dialdehyde (GDI)-modified CHIT.
75 e (GDH) in the CNT-CHIT films using glutaric dialdehyde (GDI).
76 tosan chains, and cross-linked with glutaric dialdehyde (GDI).
77 3D-printed bioinks, pre-crosslinked alginate-dialdehyde gelatin (ADA-GEL) and a mixture of alginate,
78                  We show here that the small dialdehyde glyoxal can successfully replace PFA Despite
79                      Here, we deploy the 1,2-dialdehyde glyoxal to generate antiviral nucleoside prod
80 udies on the macrocyclization of alpha,omega-dialdehydes have revealed a strong dependence on ring si
81 lls with the methylation inhibitor adenosine dialdehyde, ICP27 export to the cytoplasm occurred earli
82 ldehyde-treated cytosol and bound [32P]NADPH dialdehyde in a specific fashion.
83 s the conversion of zeaxanthin into crocetin-dialdehyde in Crocus.
84 protection step, condensation with a pyrrole dialdehyde in TFA-CH(2)Cl(2) gave the azuliporphyrin sys
85 hoxyazulitripyrrane condensed with a pyrrole dialdehyde in the presence of TFA, followed by oxidation
86                      Reaction with a pyrrole dialdehyde in the presence of TFA, followed by oxidation
87 n synthesized from an annulated cyclopropane dialdehyde intermediate.
88 angement proceeds through an unsaturated 1,4-dialdehyde intermediate.
89 here derives from a single, readily prepared dialdehyde intermediate.
90 methylformamide to give the required fulvene dialdehyde intermediates.
91  to give the crucial neo-confused dipyrrolic dialdehyde intermediates.
92 apors using the sprayed-on phenylenevinylene dialdehydes is superb and allows the identification of d
93 nds (alkanals, alkenals, Strecker aldehydes, dialdehydes, ketones and furan aldehydes) with regard to
94 hatic C5 semi- or dialdehyde, e.g., glutaric dialdehyde (Km = 1 mM).
95     The subcomponent self-assembly of a bent dialdehyde ligand and different cationic and anionic tem
96 s from a primary monoamine, Fe(II) ions, and dialdehyde ligand strands that differ in length and stru
97 -aminophenyl)benzene (TAPB) and a variety of dialdehyde linear building blocks including terephthalal
98 es (SN) via the silylated amine and glutaric dialdehyde links.
99                                Additionally, dialdehydes may have accelerated reactions in particles,
100             Herein, we show ALKBH7 regulates dialdehyde metabolism, which impacts the cardiac respons
101 acterized by reactive alpha,beta-unsaturated dialdehyde moieties, including the drimane sesquiterpene
102               Incorporation of a naphthalene-dialdehyde moiety into the delta antagonist, 6'-aminonal
103 NNA) that contains a fluorogenic naphthalene dialdehyde moiety to identify neighboring lysine and cys
104  3] imine cages with the aid of a deuterated dialdehyde molecular building block.
105 atization of the latter with naphthalene-2,3-dialdehyde (NDA) and quantification by reverse-phase hig
106 r containing a basic solution of naphthalene dialdehyde (NDA) and taurine.
107 re encountered in the preparation of fulvene dialdehydes needed for the synthesis of novel porphyrin
108 ted glycolurils or a glycoluril dimer with a dialdehyde (o-phthalaldehyde) delivers S-shaped dimers a
109                           On the other hand, dialdehyde obtained from the oxidation of 1,6-diol was f
110 blocks including terephthalaldehyde (TA) and dialdehydes of thienothiophene (TT), benzodithiophene (B
111   The influence of the regioisomerism of the dialdehydes on their photochemical behavior is profound,
112 ing multiple reactive carbonyl groups (e.g., dialdehyde or triketone) can be selectively monoallylate
113 utyllithium, addition of aldehydes, ketones, dialdehydes, or diketones at -78 C, and warming to 80 C
114 droxy-TBOH; 0.7 mg), and a ring-opened 11,12-dialdehyde oxidation product (TBOH-11,12-dialdehyde; 1.0
115                                              Dialdehyde Persian gum (PG) was applied to reinforce the
116 lhomocysteine hydrolase inhibitor (adenosine dialdehyde) potentiated toxicity of the Ado/CF combinati
117 es were obtained by postfunctionalization of dialdehyde precursor 1 using Knoevenagel condensation.
118 y crystallography confirmed that the fulvene dialdehyde precursor does have the correct geometry to f
119       In the key transformation, a protected dialdehyde precursor undergoes a cascade reaction to ins
120 hat the conversion of zeaxanthin to crocetin dialdehyde proceeds via the C30 intermediate 3-OH-beta-a
121                  The 1,8-naphthyridine-based dialdehyde promoted the formation of [2]catenanes and tr
122                                    A pyrrole dialdehyde reacted under these conditions to give sapphy
123                            The furan-derived dialdehyde reacted with a dipyrrylmethane in the presenc
124 mily was purified from liver as an aflatoxin dialdehyde reductase AKR7A1.
125 thylamine (1) with formaldehyde and glutaric dialdehyde, respectively, afforded intermediates 2 and 6
126 zed by condensation of two triamines and two dialdehydes separately.
127 es in the presence of Bu(2)BOTf, and azulene dialdehydes similarly reacted to give fulvene dialdehyde
128  modified with ascorbic acid or caffeine and dialdehyde starch (DS) were evaluated towards their appl
129 orporation influence the film stiffness, and dialdehyde starch causes an increase in brittleness.
130 rameworks (Mg-ALN MOF) embedded in a gelatin/dialdehyde starch network can simultaneously suppress bo
131  The cross-linking and hydrophobic effect of dialdehyde starch on starch-based films was proven.
132 he hydrogen-bonding ability of a BINOL-based dialdehyde subcomponent dictated the stereochemical outc
133 havior when mixed with another, short linear dialdehyde subcomponent, switching the outcome of the sy
134 ed by the condensation of linear diamine and dialdehyde subcomponents around copper(I) templates in t
135       The condensation of linear diamine and dialdehyde subcomponents around copper(I) templates in t
136 orescent bis(DTF)-PI into highly fluorescent dialdehyde-substituted PI.
137  This reaction has been extended to aromatic dialdehydes, such as terephthalic dicarboxaldehyde and i
138  addition reactions to the latent C(7)-C(11) dialdehyde synthon.
139  between a previously unreported phenoxazine dialdehyde tag and a single tyrosine site, even in the p
140 veloped based on the reaction of naphthalene dialdehyde, taurine, and cyanide, yielding a fluorescent
141 s with o-bromoaryl aldehydes to furnish aryl dialdehydes that are converted to larger polycyclic arom
142 tions or the methylation inhibitor adenosine dialdehyde, the interaction of ICP27 with SRPK1 and Aly/
143 macrocyclic products with furan or thiophene dialdehydes, they afforded tetraphenyl heterobenziporphy
144  acid-catalyzed condensations with a pyrrole dialdehyde to afford good yields of diphenylbenziporphyr
145 n, this was condensed with a dipyrrylmethane dialdehyde to afford the adj-difluoranthoporphyrin 18.
146 d benzitripyrrane was reacted with a pyrrole dialdehyde to give an aromatic hydroxyoxybenziporphyrin.
147 tection step, these condensed with a pyrrole dialdehyde to give the related azuliporphyrins in 45-51%
148 , Brilliant Blue G or periodate oxidized ATP dialdehyde to the site of ATP release in the anterior hy
149 h pyrrole, furan, thiophene, and selenophene dialdehydes to give unstable porphyrinoids that were fur
150 y able to restore the activity lost in NADPH dialdehyde-treated cytosol and bound [32P]NADPH dialdehy
151  proteins present in extracts from adenosine dialdehyde-treated RAT1 cells.
152                                        NADPH dialdehyde treatment of cytosol resulted in the loss of
153 e substituted azulenes can be converted into dialdehydes under Vilsmeier-Haack conditions, and these
154                   Bis(pyrrolylmethyl)azulene dialdehydes underwent intramolecular McMurry coupling, a
155 benzoate), which was linked with benzene-1,4-dialdehyde using imine condensation reactions, typical o
156 carbocyclic sugars from carbohydrate-derived dialdehydes using organocatalysis has been developed.
157   In a model study, an azulenylmethylpyrrole dialdehyde was condensed with a dipyrrylmethane in the p
158  preference of one triamine for a particular dialdehyde was further probed by transforming a non-pref
159 C, and the required furan-containing fulvene dialdehyde was isolated in 46% yield.
160                      McMurry coupling of the dialdehyde was successfully employed, for the first time
161                          c-Annulated pyrrole dialdehydes were also condensed with a carbatripyrrin to
162                                          The dialdehydes were condensed with dipyrrylmethanes in TFA/
163                                          The dialdehydes were investigated with respect to their amin
164 s derived from an aliphatic diamine and aryl dialdehydes were synthesized and subjected to exchange r
165                 The combination of isoindigo dialdehyde with a planar triazine core, leads to the for
166   However, condensation of the chrysopyrrole dialdehyde with a series of tripyrranes afforded excelle
167 lyzed condensation of a naphtho[2,3-f]indane dialdehyde with a tripyrrane, followed by an oxidation s
168      Acid-catalyzed condensation of a pyrene dialdehyde with a tripyrrane, followed by oxidation with
169                      Treatment of the pyrene dialdehyde with phenylmagnesium bromide generated a dica
170 t ICL formation involves condensation of the dialdehyde with the exocyclic amine.
171        MacDonald "2 + 2" condensation of the dialdehydes with a dipyrrylmethane afforded a dihydropor
172 d "2 + 2" condensation of three benzophenone dialdehydes with a dipyrrylmethane gave oxophlorin analo
173                                  Reaction of dialdehydes with a known tetrapyrrole intermediate 11b i
174                                      Pyrrole dialdehydes with fused phenanthrene or acenaphthylene ri
175 he unusual reactivity of carborane mono- and dialdehydes with pyrroles in the presence of acid cataly
176 nvolved carrying out the condensation of the dialdehydes with the tetrapyrrole in TFA-dichloromethane
177                                         Both dialdehydes yield on reaction with OH- ions geminal diol

 
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