ライフサイエンスコーパス: sodium borohydride

1 nts: 1-butyl-3-methylimidazolium bromide and sodium borohydride.

2 than the wild-type enzyme in the presence of sodium borohydride.

3 an subsequently be trapped by reduction with sodium borohydride.

4 zardous reducing agents such as hydrazine or sodium borohydride.

5 or into 2-amino-1,3-diols by reduction with sodium borohydride.

6 duction of p-nitrophenol to p-aminophenol by sodium borohydride.

7 entical sample after complete reduction with sodium borohydride.

8 lowed by reduction of the adsorbed salt with sodium borohydride.

9 the corresponding alcohols by reduction with sodium borohydride.

10 eans of either acetylation or reduction with sodium borohydride.

11 onverted to active MCRred1 by treatment with sodium borohydride.

12 water sample with a gold nanorod solution in sodium borohydride.

13 duction of methylene blue in the presence of sodium borohydride.

14 her reduced and stabilized by treatment with sodium borohydride.

15 d by oxidation and subsequent reduction with sodium borohydride.

16 reduction of an alpha-nitro ester by TiCl(3)/sodium borohydride.

17 henylalkyl halide followed by reduction with sodium borohydride.

18 imilar form can be trapped by reduction with sodium borohydride.

19 ent protein-DNA complexes in the presence of sodium borohydride.

20 equential treatment with iodosylbenzene then sodium borohydride.

21 eactions were carried out in the presence of sodium borohydride.

22 base intermediates trapped by reduction with sodium borohydride.

23 e fractionation and chemical reduction using sodium borohydride.

24 DNA complex can be trapped by reduction with sodium borohydride.

25 Reduction of mitomycin C (40 microm) by sodium borohydride (200 microm) in 20 mm Tris-HCl, 1 mm

26 t enzyme-DNA intermediate in the presence of sodium borohydride, a new finding that supports the grou

27 rocedure, incorporating derivatization using sodium borohydride, allowed the development of a sensiti

28 ing known lactones by one-pot reduction with sodium borohydride and boron trifluoride etherate.

29 e chemical reduction using sodium amalgam or sodium borohydride and enzymatic generation from porphob

30 he 6-bromo substituent was accomplished with sodium borohydride and palladium chloride.

31 (3) SgcC4 is strongly inhibited by sodium borohydride and potassium cyanide, but preincubat

32 ment of the ring-D dienone successively with sodium borohydride and singlet oxygen.

33 -elimination under alkaline conditions using sodium borohydride and sodium hydroxide.

34 n to give materials that upon reduction with sodium borohydride and subsequent hydrolysis decarboxyla

35 in carbonyls were derivatized with tritiated sodium borohydride and the tritiated proteins were separ

36 ososes were stereospecifically reduced using sodium borohydride and then deprotected to give allo- an

37 ducts of their reaction with sodium cyanide, sodium borohydride, and methoxylamine and by the mass sp

38 2'-deoxyuridine, followed by reduction with sodium borohydride as a limiting reagent, produces dTHU

39 Sodium borohydride-based hydride generation was automate

40 ng rates of sugar-aldehyde reduction and the sodium borohydride concentration dependence of the rate

41 ethyl-3-ketoacyl triketide intermediate with sodium borohydride confirmed that in each case the trike

42 ell extract and BER intermediate as bait for sodium borohydride crosslinking.

43 umin (HSA) in vitro; (ii) to determine, by a sodium borohydride-dependent mass peptide mapping method

44 hate did not stimulate and hydroxylamine and sodium borohydride did not inhibit the enzyme activity,

45 in-2(3H)-ones 21a-d, which were converted by sodium borohydride directly into optically active 3-subs

46 ch mutacin 1140 was chemically modified with sodium borohydride followed by ethanethiol, allowing the

47 curial products with O(2) in the presence of sodium borohydride furnished 72, which was readily separ

48 with Grignard reagents, sodium cyanide, and sodium borohydride gave 1,2,3,4-tetrahydropyrrolo[1,2-a]

49 eridin-1-yl)oxyl (TEMPO), ascorbic acid, and sodium borohydride) have been investigated to eliminate

50 on was determined by chemical reactions with sodium borohydride, hydrogen peroxide, alpha-methoxy-alp

51 ifying band 3 with Woodward's reagent K plus sodium borohydride (i.e., the modification process) expo

52 ketones that are capable of being reduced by sodium borohydride in an aqueous medium.

53 elds an enol ester that cannot be reduced by sodium borohydride in an aqueous solution, while other n

54 bsequently to the dianion was achieved using sodium borohydride in ethanol.

55 typhimurium enzyme by phosphonoacetaldehyde-sodium borohydride-induced inactivation and by site-dire

56 idazol-2-ones 17a-c, which were converted by sodium borohydride into (3S,7aR)-3-substituted-1-(4-nitr

57 ive site, and treatment of such adducts with sodium borohydride irreversibly inactivated the enzyme.

58 rly, reduction of the HemA-PLP complex using sodium borohydride led to > 90% inactivation of the enzy

59 This sodium borohydride-mediated reduction process resulted i

60 oxide, followed by sequential treatment with sodium borohydride, methanesulfonyl chloride, and morpho

61 dified by WR-K and then reduced by tritiated sodium borohydride (NaB[3H]4) showed the presence of a p

62 of HInCl(2) from the reduction of InCl(3) by sodium borohydride (NaBH(4)) was also re-evaluated for c

63 using the chemical precipitation method with sodium borohydride (NaBH4) as the reductant in the prese

64 Janus microparticle motors in a solution of sodium borohydride (NaBH4) fuel.

65 tion of AgNPs onto silica using a chitosan + sodium borohydride (NaBH4) method results in higher silv

66 Specifically, we use a sodium borohydride (NaBH4) treatment process to thorough

67 hod with varying amounts of reductant, i.e., sodium borohydride (NaBH4).

68 zole, an alkylating agent (usually MeI), and sodium borohydride (NaBH4).

69 330, which is obtained by reducing F430 with sodium borohydride (NaBH4).

70 of a lipid fraction derived from oxLDL with sodium borohydride or potassium iodide completely abroga

71 tones/aldehydes to alcohols employing excess sodium borohydride produced pronounced and largely, but

72 ent on-line hydride generation with acid and sodium borohydride produces AsH3 and H2, which are separ

73 e removal of the chiral auxiliary in 5 using sodium borohydride, protection of the gamma-cyano alcoho

74 the DAB-enhanced stain was used; it utilizes sodium borohydride, proteinase K, Triton X-100 and xylen

75 eveal regions of the sample matrix where the sodium borohydride-reduced silver colloidal particles ar

76 (GUS) with sodium metaperiodate followed by sodium borohydride reduction (PerT-GUS) eliminated uptak

77 followed by treatment with sodium azide and sodium borohydride reduction gave 5-azido-5-hydroxylmeth

78 Hence, the sodium borohydride reduction of hemiacetals 2a,b can be

79 l oligosaccharides were released by alkaline sodium borohydride reduction of the jelly coating from t

80 Sodium borohydride reduction operates from the beta-face

81 e GalNAc residues by periodate oxidation and sodium borohydride reduction, indicating a requirement f

82 droxymethylcytosine and, in combination with sodium borohydride reduction, single 5-formylcytosine nu

83 glycan release to promote lactonization, and sodium borohydride reduction, that were both optimized t

84 bose-5-phosphate-containing DNA substrate by sodium borohydride reduction.

85 ntly linked to the 8-oxoG oligonucleotide by sodium borohydride reduction.

86 ction of MSOX or MTOX with a small excess of sodium borohydride results in immediate flavin reduction

87 In this study, treatment of CBS with sodium borohydride selectively reduced the Schiff base b

88 sis using COS cells lysed in the presence of sodium borohydride showed that: 1) phosphate recovered o

89 Treatment of galactated HSA with sodium borohydride stabilized the condensed sugars on th

90 uggested a cyclic moiety, and reduction with sodium borohydride suggested two reducible oxygen-contai

91 tivated upon exposure to pyridoxal phosphate/sodium borohydride, suggesting a reactive lysine residue

92 1-arylcyclohexadienyliron(1+) complexes with sodium borohydride to access the endo series also gave a

93 can be reduced by either triethyl silane or sodium borohydride to form the corresponding beta- and g

94 atives and could be selectively reduced with sodium borohydride to give unstable benziphlorins.

95 y chemical reduction of the silver ions with sodium borohydride to produce silver particles.

96 he benzene rings, followed by treatment with sodium borohydride to reduce the nitro-groups to primary

97 Schiff base intermediate that can react with sodium borohydride to trap the DNA-enzyme complex.

98 Sodium borohydride trapping of wild-type Fpg and its E3Q

99 x sample matrices was accounted for by using sodium borohydride-treated blanks.

100 t disrupted by increased temperature because sodium borohydride treatment of the enzyme at either 15

101 Sodium borohydride treatment reduces M(1)GdR to the 5,6-

102 1 complex and reactivity to decreased pH and sodium borohydride treatment were suggestive of a struct

103 onment, bioreductants, exogenous thiols, and sodium borohydride were studied.

104 a mixture of 6 M guanidine hydrochloride and sodium borohydride, which stopped the reaction and reduc

105 l was carried out using aqueous solutions of sodium borohydride, which yielded a refractive index sen

106 Reduction of thiocolchiocone with sodium borohydride yielded the racemic alcohol 9, the st