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1 DNA complex can be trapped by reduction with sodium borohydride.
2 than the wild-type enzyme in the presence of sodium borohydride.
3 eans of either acetylation or reduction with sodium borohydride.
4 an subsequently be trapped by reduction with sodium borohydride.
5 ] or 2-(3-oxoindolin-2-yl)acetonitriles with sodium borohydride.
6 duction of methylene blue in the presence of sodium borohydride.
7 equential treatment with iodosylbenzene then sodium borohydride.
8 e fractionation and chemical reduction using sodium borohydride.
9 tionality in the same pot by the addition of sodium borohydride.
10 zardous reducing agents such as hydrazine or sodium borohydride.
11  or into 2-amino-1,3-diols by reduction with sodium borohydride.
12 duction of p-nitrophenol to p-aminophenol by sodium borohydride.
13 entical sample after complete reduction with sodium borohydride.
14 lowed by reduction of the adsorbed salt with sodium borohydride.
15 the corresponding alcohols by reduction with sodium borohydride.
16 onverted to active MCRred1 by treatment with sodium borohydride.
17 water sample with a gold nanorod solution in sodium borohydride.
18 her reduced and stabilized by treatment with sodium borohydride.
19 ) and reduced to the corresponding amines by sodium borohydride.
20 d by oxidation and subsequent reduction with sodium borohydride.
21 reduction of an alpha-nitro ester by TiCl(3)/sodium borohydride.
22 henylalkyl halide followed by reduction with sodium borohydride.
23 imilar form can be trapped by reduction with sodium borohydride.
24 ent protein-DNA complexes in the presence of sodium borohydride.
25 eactions were carried out in the presence of sodium borohydride.
26 nts: 1-butyl-3-methylimidazolium bromide and sodium borohydride.
27 base intermediates trapped by reduction with sodium borohydride.
28      Reduction of mitomycin C (40 microm) by sodium borohydride (200 microm) in 20 mm Tris-HCl, 1 mm
29 t enzyme-DNA intermediate in the presence of sodium borohydride, a new finding that supports the grou
30 rocedure, incorporating derivatization using sodium borohydride, allowed the development of a sensiti
31 ing known lactones by one-pot reduction with sodium borohydride and boron trifluoride etherate.
32 e chemical reduction using sodium amalgam or sodium borohydride and enzymatic generation from porphob
33 he 6-bromo substituent was accomplished with sodium borohydride and palladium chloride.
34           (3) SgcC4 is strongly inhibited by sodium borohydride and potassium cyanide, but preincubat
35 ment of the ring-D dienone successively with sodium borohydride and singlet oxygen.
36 -elimination under alkaline conditions using sodium borohydride and sodium hydroxide.
37 n to give materials that upon reduction with sodium borohydride and subsequent hydrolysis decarboxyla
38 in carbonyls were derivatized with tritiated sodium borohydride and the tritiated proteins were separ
39 ososes were stereospecifically reduced using sodium borohydride and then deprotected to give allo- an
40 ducts of their reaction with sodium cyanide, sodium borohydride, and methoxylamine and by the mass sp
41  2'-deoxyuridine, followed by reduction with sodium borohydride as a limiting reagent, produces dTHU
42 zatriphenylenehexacarbonitrile [HAT(CN)(6) ] sodium borohydride as the starting materials.
43                   The reducibility of DOM by sodium borohydride (as judged by relative removal of ini
44                                              Sodium borohydride-based hydride generation was automate
45 when activated with a hydride source such as sodium borohydride, cleanly and selectively dehalogenate
46 ng rates of sugar-aldehyde reduction and the sodium borohydride concentration dependence of the rate
47 ethyl-3-ketoacyl triketide intermediate with sodium borohydride confirmed that in each case the trike
48 ell extract and BER intermediate as bait for sodium borohydride crosslinking.
49 umin (HSA) in vitro; (ii) to determine, by a sodium borohydride-dependent mass peptide mapping method
50 hate did not stimulate and hydroxylamine and sodium borohydride did not inhibit the enzyme activity,
51 in-2(3H)-ones 21a-d, which were converted by sodium borohydride directly into optically active 3-subs
52 ch mutacin 1140 was chemically modified with sodium borohydride followed by ethanethiol, allowing the
53 curial products with O(2) in the presence of sodium borohydride furnished 72, which was readily separ
54  with Grignard reagents, sodium cyanide, and sodium borohydride gave 1,2,3,4-tetrahydropyrrolo[1,2-a]
55                                  Addition of sodium borohydride generates a hydroquinone derivative t
56 ction of dissolved organic matter (DOM) with sodium borohydride has been used to understand the geogr
57 eridin-1-yl)oxyl (TEMPO), ascorbic acid, and sodium borohydride) have been investigated to eliminate
58 on was determined by chemical reactions with sodium borohydride, hydrogen peroxide, alpha-methoxy-alp
59 ifying band 3 with Woodward's reagent K plus sodium borohydride (i.e., the modification process) expo
60 ketones that are capable of being reduced by sodium borohydride in an aqueous medium.
61 elds an enol ester that cannot be reduced by sodium borohydride in an aqueous solution, while other n
62 bsequently to the dianion was achieved using sodium borohydride in ethanol.
63  typhimurium enzyme by phosphonoacetaldehyde-sodium borohydride-induced inactivation and by site-dire
64 idazol-2-ones 17a-c, which were converted by sodium borohydride into (3S,7aR)-3-substituted-1-(4-nitr
65 ive site, and treatment of such adducts with sodium borohydride irreversibly inactivated the enzyme.
66 rly, reduction of the HemA-PLP complex using sodium borohydride led to > 90% inactivation of the enzy
67                                         This sodium borohydride-mediated reduction process resulted i
68 oxide, followed by sequential treatment with sodium borohydride, methanesulfonyl chloride, and morpho
69 dified by WR-K and then reduced by tritiated sodium borohydride (NaB[3H]4) showed the presence of a p
70 ohols are obtained in very good yields using sodium borohydride (NaBH(4)) as a reducing agent and a c
71 remove major tRNA modifications, followed by sodium borohydride (NaBH(4)) reduction of m(7)G sites an
72 of HInCl(2) from the reduction of InCl(3) by sodium borohydride (NaBH(4)) was also re-evaluated for c
73 s of 4-nitrophenol (4-NP) in the presence of sodium borohydride (NaBH(4)).
74 using the chemical precipitation method with sodium borohydride (NaBH4) as the reductant in the prese
75  Janus microparticle motors in a solution of sodium borohydride (NaBH4) fuel.
76 tion of AgNPs onto silica using a chitosan + sodium borohydride (NaBH4) method results in higher silv
77                       Specifically, we use a sodium borohydride (NaBH4) treatment process to thorough
78 hod with varying amounts of reductant, i.e., sodium borohydride (NaBH4).
79 zole, an alkylating agent (usually MeI), and sodium borohydride (NaBH4).
80 330, which is obtained by reducing F430 with sodium borohydride (NaBH4).
81 tions are performed using dissolving metals, sodium borohydride or hydrogen transfer conditions under
82  of a lipid fraction derived from oxLDL with sodium borohydride or potassium iodide completely abroga
83 tones/aldehydes to alcohols employing excess sodium borohydride produced pronounced and largely, but
84 ent on-line hydride generation with acid and sodium borohydride produces AsH3 and H2, which are separ
85 e removal of the chiral auxiliary in 5 using sodium borohydride, protection of the gamma-cyano alcoho
86 the DAB-enhanced stain was used; it utilizes sodium borohydride, proteinase K, Triton X-100 and xylen
87 ompounds were initially converted to stable, sodium borohydride-reduced 3-aminopyridine conjugates, w
88 eveal regions of the sample matrix where the sodium borohydride-reduced silver colloidal particles ar
89  (GUS) with sodium metaperiodate followed by sodium borohydride reduction (PerT-GUS) eliminated uptak
90  followed by treatment with sodium azide and sodium borohydride reduction gave 5-azido-5-hydroxylmeth
91                                   Hence, the sodium borohydride reduction of hemiacetals 2a,b can be
92 l oligosaccharides were released by alkaline sodium borohydride reduction of the jelly coating from t
93   Additionally, by predicting the effects of sodium borohydride reduction on the model compounds and
94                                              Sodium borohydride reduction operates from the beta-face
95 small RNA selection, AlkB demethylation, and sodium borohydride reduction steps to achieve specific a
96 e GalNAc residues by periodate oxidation and sodium borohydride reduction, indicating a requirement f
97 droxymethylcytosine and, in combination with sodium borohydride reduction, single 5-formylcytosine nu
98 glycan release to promote lactonization, and sodium borohydride reduction, that were both optimized t
99 ntly linked to the 8-oxoG oligonucleotide by sodium borohydride reduction.
100 ken at breaking point, both with and without sodium borohydride reduction.
101 bose-5-phosphate-containing DNA substrate by sodium borohydride reduction.
102 ction of MSOX or MTOX with a small excess of sodium borohydride results in immediate flavin reduction
103         In this study, treatment of CBS with sodium borohydride selectively reduced the Schiff base b
104 sis using COS cells lysed in the presence of sodium borohydride showed that: 1) phosphate recovered o
105 to its original state after treatment with a sodium borohydride solution, demonstrating the reversibl
106             Treatment of galactated HSA with sodium borohydride stabilized the condensed sugars on th
107 uggested a cyclic moiety, and reduction with sodium borohydride suggested two reducible oxygen-contai
108 tivated upon exposure to pyridoxal phosphate/sodium borohydride, suggesting a reactive lysine residue
109 1-arylcyclohexadienyliron(1+) complexes with sodium borohydride to access the endo series also gave a
110  can be reduced by either triethyl silane or sodium borohydride to form the corresponding beta- and g
111 atives and could be selectively reduced with sodium borohydride to give unstable benziphlorins.
112 y chemical reduction of the silver ions with sodium borohydride to produce silver particles.
113 he benzene rings, followed by treatment with sodium borohydride to reduce the nitro-groups to primary
114 Schiff base intermediate that can react with sodium borohydride to trap the DNA-enzyme complex.
115                                              Sodium borohydride trapping of wild-type Fpg and its E3Q
116 x sample matrices was accounted for by using sodium borohydride-treated blanks.
117 t disrupted by increased temperature because sodium borohydride treatment of the enzyme at either 15
118                                              Sodium borohydride treatment reduces M(1)GdR to the 5,6-
119 1 complex and reactivity to decreased pH and sodium borohydride treatment were suggestive of a struct
120 onment, bioreductants, exogenous thiols, and sodium borohydride were studied.
121 a mixture of 6 M guanidine hydrochloride and sodium borohydride, which stopped the reaction and reduc
122 l was carried out using aqueous solutions of sodium borohydride, which yielded a refractive index sen
123 alyze these imine bonds after reduction with sodium borohydride while under tension and found that th
124            Reduction of thiocolchiocone with sodium borohydride yielded the racemic alcohol 9, the st

 
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