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1 ep, rather than the previously described two-step reaction.
2 t the second (rearrangement) step of the two-step reaction.
3 t plasminogen is converted to AS4.5 in a two-step reaction.
4 t this mode of chromatin remodeling is a two-step reaction.
5  analog was prepared similarly, but in a two step reaction.
6  reduced to 1-hexadecanol by LiAlH4 in a one-step reaction.
7 ase A2 and were synthesized in a one-pot two-step reaction.
8  to reversible self-cleavage but was a three-step reaction.
9 ing a one-pot hydrothermal method via single-step reaction.
10 in contrast to DB-JBP1, which binds in a one-step reaction.
11 sized in high yields on gram scales in a one-step reaction.
12        Binding of gHgL to integrins is a two-step reaction.
13 entrance and the heme group during the three-step reaction.
14  the transformation of AA to LTA(4) in a two-step reaction.
15 erted into the substrate via a consecutive 2-step reaction.
16 -Cryp) was successfully synthesized by a one-step reaction.
17 es the formation of NO via a consecutive two-step reaction.
18 activation of acetate to acetyl-CoA in a two-step reaction.
19 2).(diamine)] can be synthesized in a single-step reaction.
20 difficult, particularly in complicated multi-step reactions.
21 location as a sequence of coupled hydrolysis-stepping reactions.
22                                  Using a one-step reaction, a bifunctional compound was synthesized f
23                             The one-pot, two-step reaction also worked with electron-rich hydroxy- an
24 peak, is easily synthesized via a simple one-step reaction and is formulated in water with high stabi
25 ycloisomerization becomes a complex multiple-step reaction and proceeds with a rate-determining barri
26 ins can be more complex than a simple single-step reaction, and that application of several methods c
27 hereas the discrimination in the overall two-step reaction arises from very weak binding of noncognat
28 were obtained in quantitative yield in a one-step reaction at ambient temperature from the commercial
29  DnaK-peptide complexes according to the two-step reaction, ATP + DnaK-P if ATP-DnaK-P if ATP-DnaK +
30 f the reaction course indicate a virtual one-step reaction between the NHC and the silanorbornadiene.
31     Protein splicing proceeds through a four-step reaction but the catalytic mechanism is not fully u
32 ediators formed from arachidonic acid in a 2-step reaction catalyzed by 5-lipoxygenase (5-LOX) requir
33 rom soluble Mn(II) to Mn(IV) oxides is a two-step reaction catalyzed by an MCO-containing complex.
34  reaction is a "simple" extension of the two-step reaction catalyzed by MR: base-catalyzed proton abs
35 , indicating that ester production was a two-step reaction consisting of hydrolysis and esterificatio
36 -chlorobenzoyl-coenzyme A formation in a two-step reaction consisting of the adenylation of 4-chlorob
37 red reaction pathway, compared to the single-step reaction, constitute the key advantages of this tan
38                                  In this two-step reaction, first-strand scission is mediated by a nu
39  the behavior of KIEobs for a reversible two-step reaction for all possible values of the rate consta
40     In this Communication, we describe a two-step reaction for preparing three-dimensional electrodes
41 strate availability, we also developed a two-step reaction for the enzymatic synthesis of UDP-l-rhamn
42     Under a new approach, we developed a one step reaction for the interconversion of artemisinin 1 i
43 g intermediate participates in normal second-step reactions, forming spliced exon and linear intron R
44 ing deterrent that can be formed in a single step reaction from 3-dehydroquinate catalyzed by quinate
45                             The combined two step reaction gave a radiochemical yield of 10-15% (EOB)
46                             The overall four-step reaction gave higher yields (57%) than the two-step
47 gens to estrogens through a sequential three-step reaction, generating 19-hydroxy and 19-aldehyde int
48          A mechanism is proposed for the two-step reaction governed by the synthetase, in which His41
49         PASP-IO nanoparticles made by single-step reaction have a core size of 5 nm with a hydrodynam
50 70 complex rapidly binds hsp90 in the second step reaction in a nucleotide-independent manner.
51  of highly sulfated keratan sulfate by a two-step reaction in vitro with a mixture of beta3GnT7/beta4
52 ts in tyrosine nitration, catalyzed as a two-step reaction in which nitric-oxide synthase induction i
53 alysis of PCNA opening by RFC revealed a two-step reaction in which RFC binds PCNA before opening PCN
54                                This is a two-step reaction in which the enzyme first condenses with G
55        Formation of pyruvate by SDH is a two-step reaction in which the hydroxyl group of serine is c
56 halose biosynthesis in plants involves a two-step reaction in which trehalose-6-phosphate (T6P) is sy
57 onine S-adenosyltransferase) catalyzes a two-step reaction in which tripolyphosphate (PPPi) is a tigh
58 ediate species in total, we map out relevant step reactions in a model size growth reaction from mole
59 synthetic history-that is, a complete set of step reactions in their synthetic routes.
60 h seven 1,3,5-triazines was studied in a one-step reaction (in situ formation of 3-aminopyrrole) and
61 BP1 binds to J-DNA or glu-5-hmC-DNA in a two-step reaction, in contrast to DB-JBP1, which binds in a
62 f class II synthetases and carries out a two-step reaction, in which lysine is activated by being att
63 xperiments and computations indicate a three-step reaction including isomerization of diazomethane, a
64 tic resonance spectroscopy, with temperature-step reaction initiation, starting from the enzyme-coenz
65 ring progress of the decay after temperature step reaction initiation.
66 sor messenger RNA (pre-mRNA) splicing, a two-step reaction involved in a multitude of RNA structural
67 ab' fragments was also consistent with a two-step reaction involving fast high-affinity binding and a
68 s the addition of water to epoxides in a two-step reaction involving initial attack of an active site
69 slational modification is performed in a two-step reaction involving the addition of a beta-lysine mo
70 midation of bioactive peptides through a two-step reaction involving the monooxygenase and lyase doma
71 presence of both catalyst and solvent, a two-step reaction is predicted, corresponding to the stepwis
72 hase (NOS) generates NO via a sequential two-step reaction [l-arginine (l-Arg) --> N-hydroxy-l-argini
73                               The elementary step reaction mechanism derived from this comprehensive
74 ld and made it possible to demonstrate a two-step reaction mechanism for des-PPW with K init = 10.4 +
75           The data support the proposed four-step reaction mechanism of ACDs, coupling acyl-CoA thioe
76                                     This two-step reaction mechanism of the widely used Amplex Red, a
77                                       A five-step reaction mechanism was used to account for the obse
78 inds single-headed myosin VI following a two-step reaction mechanism with formation of a low affinity
79 er the entire temperature range with a three-step reaction mechanism, originally proposed by Ashton e
80    However, kinetic modeling indicated a two-step reaction mechanism, with formation of peroxocarbona
81 sociation of a protein complex follows a two step reaction mechanism, with the first step being the f
82 aBH(4)-sensitive intermediate suggests a two-step reaction mechanism.
83 ng atomic resolution images) reveals a three-step reaction mechanism.
84 nick, is the rate-limiting step in the multi-step reaction mediated by hNTH1.
85 cient alternative pathway in which the first-step reaction occurs by hydrolysis.
86 spliceosomal and group II introns, the first-step reaction occurs by nucleophilic attack on the 5' sp
87 0 Da poly(propylene fumarate) (PPF) by a two-step reaction of diethyl fumarate and propylene glycol t
88  substituents are synthesized by using a one-step reaction of H(8)BINOL with amino methanols that wer
89 e DFT-level mechanism elucidation of the two-step reaction of non-heteroatom-stabilized carbenes with
90                                      The one-step reaction of some amino-substituted heterocycles wit
91                                One-pot three-step reactions of 50, 51, and 56 provided the desired 3'
92                        Resolution of the two-step reactions of AT and AT-Denver with wild-type and mu
93                        Resolution of the two-step reactions of AT with the mutant thrombins revealed
94                                  In the next step, reaction of the sugar-derived (Z)-1-bromo-1-nitroa
95 athway comprising three nucleotidyl transfer steps: reaction of Rtc with ATP to form a covalent Rtc-(
96 d carbon dioxide can be produced in a single-step reaction over the catalyst, with no detectable CO (
97 s of ghrelin follows an unprecedented single-step reaction pathway and the single-step acylation proc
98                                   The single-step reaction pathway for the acylation is remarkably di
99            Mechanistic studies support a two-step reaction pathway involving initial dissociation of
100 s the first time demonstrating that a single-step reaction pathway is possible for an ester hydrolysi
101 tions provide evidence for an unexpected two-step reaction pathway, which involves dehydrogenative in
102 ation process must follow the well-known two-step reaction pathway.
103 ed by changes in the first on rates of a two-step reaction pathway.
104 oselectivity differences thus enabled single-step reaction pathways to an effective collection of dox
105                                      The two-step reaction progress also was monitored in real time b
106  proteins at cysteine residues, but this two-step reaction requires lengthy incubations and produces
107         The proposed derivatization is a one-step reaction, requires no organic solvents, and is safe
108  Polyadenylation of mRNA precursors is a two-step reaction requiring multiple protein factors.
109 midating monooxygenase (PAM) catalyzes a two-step reaction resulting in the C-terminal amidation of p
110                   Kinetic studies of the two-step reaction revealed that the variants show a signific
111 en-1-yl phosphonates were prepared in a five-step reaction route from beta-ketophosphonates.
112               These observations favor a two-step reaction scheme involving two complete oxidative cy
113 e other as the emitter electrode, a multiple-step reaction scheme was achieved that included consecut
114                                      A three-step reaction sequence has been developed to prepare a v
115 izidine 5,8-epi-indolizidine 223A via a five-step reaction sequence in 32% overall yield.
116                  Here we demonstrate a three-step reaction sequence in which a copper complex convert
117 fold diversity has been achieved using a two-step reaction sequence involving allylic substitution an
118 -R species, where R = H or -CH3, using a two-step reaction sequence involving chlorination of H-Si(11
119 here carbamyl phosphate is formed in a three-step reaction sequence.
120 ined in a 6.7% overall yield following an 11-step reaction sequence.
121 ne in good to excellent yields using a three-step reaction sequence.
122 n of 10 to 1 is accomplished through a three-step reaction sequence.
123 NO from L-arginine, NADPH, and O(2) in a two-step reaction sequence.
124 orts to design selective catalysts for multi-step reactions, such as hydrodeoxygenation (HDO), have e
125 -Hydroxybenzoate hydroxylase catalyzes a two-step reaction that demands precise control of solvent ac
126  on a large scale, in high yield using a one-step reaction that employs commercially available reagen
127            Beetle luciferases catalyze a two-step reaction that includes the initial adenylation of t
128  protein synthase III (FabH) catalyzes a two step reaction that initiates the pathway of fatty acid b
129 osphatidylinositol 4,5 bisphosphate in a two step reaction that involves a cyclic intermediate.
130 enzymes catalyze mechanistically similar two-step reactions that proceed through an enzyme-bound acyl
131                                   In the two-step reaction, the activated intermediate, bio-5'-AMP, i
132                            In a fast, single-step reaction, the monomeric alkoxide precursors permeat
133 imetric analysis results, which show the two-step reaction to be exothermic by -215 kJ mol(-1), in ag
134                                        A two-step reaction to convert terminal alkynes into triboryla
135 orming family of enzymes that catalyze a two-step reaction to first activate a carboxylate substrate
136 ch using LCA as a template, along with a two-step reaction to generate sodium 3-hydroxyolean-12-en-30
137 5-lipoxygenase (5-LO), which catalyzes a two-step reaction to produce leukotriene A4.
138 mines (-NH2), and this allowed for the multi-step reactions to be carried out in tandem within the MO
139 ated actin filaments in an apparently single step reaction upon binding, whereas the stabilization by
140 oups of hyaluronan are biotinylated in a one-step reaction using biotin-hydrazide.
141 ocked by stoichiometric acetylation in a one-step reaction using sulfosuccinimidyl acetate (S-NHSAc)
142  situ formation of 3-aminopyrrole) and a two-step reaction (using the tetraphenylborate salt and an a
143 dic acid is typically synthesized in a three-step reaction utilizing three enzymes: glycerol 3-phosph
144 ntibodies within minutes in a homogenous one-step reaction visible to the naked eye.
145 te kinetics applicable to realistic multiple step reactions, we present here the successful applicati
146                            Concerted and two-step reactions were designed to evaluate (+) strand prim
147  batteries, whose lithiation undergoes a two-step reaction, whereby intercalation and conversion occu
148 hibitor was shown to bind thrombin via a two-step reaction wherein the initially formed thrombin-inhi
149                        MAT catalyzes the two-step reaction which synthesizes S-adenosylmethionine (Ad
150 0 kDa) proteins was accomplished in a single-step reaction with a commercially available bis(2,2'-bip
151 ry in optically pure form using a simple one-step reaction with commercially available reagents.
152   They can be additionally modified in a one-step reaction with functional groups for covalent labeli
153 activation of the E. coli enzyme is a single-step reaction with kon = 1.94 x 10(4) M-1 s-1.
154 ther spliceosomal components, performs a two-step reaction with two short RNA oligonucleotides as sub
155 s of complexes 1 and 2 are classified as two-step reactions with an element of reversibility.
156 es RNA 2',3' cyclic phosphate ends via three steps: reaction with ATP to form a covalent RtcA-(histid
157 oth DNA substrates occurs by a minimum three-step reaction, with the bimolecular step followed by two
158 coccus triterpene synthases, catalyzes a two-step reaction within a single enzyme unit without interm

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