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1 iometric C-H amination with these copper(II) anilides.
2 activity for hydroxamic acids and orthoamino anilides.
3 hemical dehydrohalogenation of corresponding anilides.
4 veniently synthesized from reactions between anilide 1 and phenyliodine(III) diacetate (PIDA) through
5                            The unsubstituted anilide 12 had a K(i) value at A(2B) receptors of 1.48 n
6 resence of a broad scope of tertiary amides, anilide, 2-pyridone, and carbamate functionality.
7                                    Levels of anilides, 2,6-dinitroanilines, chlorophenols, triclosan,
8 -MB-231 and colon RKO cancer cell lines, the anilide 2b (salermide) and the phenylpropylthio analogue
9                                              Anilides 3b and 3c were used as vehicles to explore stru
10                              Of these 16 new anilides administered orally as one 6 mg/kg dose combine
11 hloride and bromide substituents on both the anilide and aryl iodide coupling components.
12 III)-catalyzed protocol for the amidation of anilide and enamide C-H bonds with isocyanates has been
13            The electron-transfer behavior of anilides and dianilides was studied and led to the follo
14 riflate catalyzed selective C-benzylation of anilides and heteroaryl amides with benzyl chlorides hav
15 -reported pain medications (opioids, NSAIDs, anilides, and salicylic acid).
16            The first C-H bond activation for anilide- and amide-type ligands can occur at the ortho a
17 n determines the turnover frequency for both anilide- and benzamide-type systems.
18 t k(cat)/K(m) for hydrolysis of tetrapeptide anilides at low ionic strength with a Bronsted slope alp
19 olinone rotational barriers about the chiral anilide axis were also studied using density functional
20 dem cyclizations of alpha-halo-ortho-alkenyl anilides bearing an additional substituent on the alpha-
21 pe of linkage with the pendant groups (i.e., anilide, benzamide) or the aromatic substitution pattern
22 rossover experiments established exchange of anilide (but not imido) ligands in the presence of free
23 and control of the molecular conformation of anilides by resonance effects.
24 r rare class of compounds, are prepared from anilides by the action of Dess-Martin periodinane (DMP)
25 -> pi*C horizontal lineO resonance in simple anilides can be varied by as much as 10 kcal/mol.
26 ment of Alzheimer's disease (AD) utilizes an anilide chemotype that engages a key residue (Gly230) in
27       The principal role of these copper(II) anilides [Cl2NN]Cu-NHAr is to capture the radical R(*) g
28 series of novel beta-diketiminato copper(II) anilides [Cl2NN]Cu-NHAr that participate in C-H aminatio
29 u-(t)OBu yields the corresponding copper(II) anilides [Cl2NN]Cu-NHAr.
30 f an H-atom donor cleanly affords the Co(II) anilide complex ((Tr) L)Co(NHC(6) F(5) ).
31 tivation of dihydrogen with a molecular zinc anilide complex is reported.
32 ropose that the enzyme accommodates a copper-anilide complex that reacts with a benzylic radical.
33            Reaction of the uranium(III) tris(anilide) complex (THF)U(N[t-Bu]Ar)(3) (1, THF = tetrahyd
34 ([N(n-Bu)(4)][1]) with the uranium(III) tris(anilide) complex (THF)U(N[t-Bu]Ar)(3) (2; THF = tetrahyd
35 n performed with sterically hindered aniline/anilide complexes and nitroxyl radical species.
36  reactions of Os(IV) and Os(III) aniline and anilide complexes.
37  strongly on the substituents present in the anilide component and in the aromatic ring of the aldehy
38  excited-state for the para-COPh-substituted anilide derivative and is not quenched by 0.15 M piperyl
39 human leukemia U937 cells, the benzamide and anilide derivatives 1b, 1c, 2b, and 2c as well as the 4-
40 ese antiproliferative effects is enhanced in anilide derivatives and translates into tumor growth inh
41              The optimization of a series of anilide derivatives of (R)-3,3, 3-trifluoro-2-hydroxy-2-
42                                  Sixteen new anilide derivatives of the natural trioxane artemisinin
43 mediated cyclization reaction of unsaturated anilides discovered during the total synthesis of the CP
44 ium-catalyzed intramolecular arylation of an anilide enolate.
45 io of hydrolysis of succinyl-Ala-Ala-Pro-Phe-anilides for p-nitroaniline versus aniline leaving group
46       A metal-free method for fast and clean anilide formation from perfluoroaryl azide and thioacid
47 ggesting a single electron transfer from the anilide functionality to IBX and implicating a radical-b
48 tantiate the hypothesis that the presence of anilide groups establishes a strong energetic preference
49 containing oxindoles from readily accessible anilides has been developed.
50 ith benzyl nitriles, aryl Weinreb amides and anilides have been evaluated for the transformation usin
51  oxidative addition of aniline to form a bis-anilide hydride complex, followed by migratory insertion
52               With the exception of suberoyl anilide hydroxamic acid and PXD101, all of the other HDA
53 xamic acids (oxamflatin, Scriptaid, suberoyl anilide hydroxamic acid, panobinostat [LBH589], and beli
54 hdrawing groups on the ortho position of the anilide, i.e., chloro, acetyl, or bromo, increased poten
55                    A lead aryl pyrrolidinone anilide identified using high-throughput in vivo screeni
56 ies is optimal (as measured by AUC) when the anilide is substituted at the 4-position with an electro
57  application of a novel lithium N-cyclohexyl anilide (LiCyan).
58 the inhibitor layout by series of amine- and anilide-linked pyridine p-substituents to generate addit
59  as well as the core pyrazoline ring and the anilide linker.
60                                          The anilide-methyl complex (PNP)Sc(NH[DIPP])(CH(3)) (1) [PNP
61                                 Although the anilide moiety affords excellent potency, it simultaneou
62 alicyloyl ring and hydrophobic groups in the anilide moiety for optimal activity.
63 l moiety for binding but lacked the phenolic anilide moiety.
64                 The activity of the cinnamic anilide mPTP inhibitors turned out to be additive with t
65 ethylamides (n = 2) were active, most of the anilides (n = 0) turned out to moderately or strongly in
66 adily induced spiroannulation of 2-alkynolyl anilides (n = 1-3) to form gem-dibromospirocyclic benzo[
67  monodentate amide ligands - the m-terphenyl anilides [N(R){C6H3Ar2-2,6}](-) (Ar = aryl, R = H, methy
68 ries, an acyl group at the 2-position of the anilide of these thiophene sulfonamides improved oral bi
69  easily obtained from aromatic aldehydes and anilides of dichloroacetic acid under Darzens condensati
70 ylglycine methyl ester (PGME) linked through anilide or benzamide bonds were prepared (i.e., o-, m-,
71  and aralkyl amides demonstrated that simple anilides, particularly those substituted in the para-pos
72  The palladium-catalyzed direct arylation of anilides possessing several N-acyl substituents has been
73 talysis, undergo in situ trapping to provide anilide products.
74                  No KIE or exchange with the anilide proton was observed when 1-d(3) was treated with
75 air, rt) of racemic alpha-halo-ortho-alkenyl anilides provide 3,4-dihydroquinolin-2-ones in high yiel
76     Genomic sequencing of aryl pyrrolidinone anilide-resistant Arabidopsis thaliana progeny combined
77 en by two independent pathways involving the anilide ring and amide nitrogen moieties.
78 N-chlorination and Cl(2) > HOCl > OCl(-) for anilide ring chlorination.
79                   For all four complexes the anilide rings of the inhibitors overlap aromatic rings o
80 orter isopropylmethanoyl substituents of the anilide rings of UC-38/UC-84, which draws these rings cl
81 (CSPs) containing a subset of the amino acid anilide selector library was screened for enantioselecti
82 ity and local lipophilicity), applied to the anilide series suggests structural modifications to impr
83                      Five simply substituted anilides show low-microM blockade of the MV, one of whic
84  such as glutathione (gammaGlu-Cys-Gly), and anilides, such as gamma-glutamyl-7-amido-4-methylcoumari
85 elopment of a series of substituted cinnamic anilides that represents a novel class of mitochondrial
86  Herein, we demonstrate that N-acylanilines (anilides), the first class of planar amides that have be
87  for the carboxylation of ortho-C-H bonds in anilides to form N-acyl anthranilic acids has been devel
88 tion with certain unsaturated N-aryl amides (anilides) to form heterocycles are described.
89          Addition of an H-atom to the Os(IV) anilide TpOs(NHPh)Cl(2) (Os(IV)NHPh) gives the Os(III) a
90 lyzed annulation reactions of benzamide- and anilide-type aromatic systems with maleimides is investi
91                                      For the anilide-type system, ortho and benzylic C-H bond activat
92       Palladium-catalyzed ortho-arylation of anilides was achieved using 2-aminophenyl-1H-pyrazole (2
93 gO as the promoter, mono- and diarylation of anilides were realized in up to 89% isolated yield.
94                 A library of 36 L-amino acid anilides, which are potential selectors for chiral HPLC,
95   On the other hand, trimethyl ether galloyl anilides, with few exceptions, exhibited moderate to ver
96 nzoxazinones and quinazolinones, from simple anilides without installing and removing an external dir