ライフサイエンスコーパス: phenylboronic acid

1 sides or nucleotides with 4-(trifluoroacetyl)phenylboronic acid.

2 1-one and in the deoxygenation reaction with phenylboronic acid.

3 films are functionalized with 2-(bromomethyl)phenylboronic acid.

4 compounds related to both benzoxaborole and phenylboronic acid.

5 to that previously determined for the simple phenylboronic acid.

6 role was found to differ from that of simple phenylboronic acid.

7 for cis-diols as compared with unsubstituted phenylboronic acid.

8 to the ring opened boronate by reaction with phenylboronic acid.

9 ki carbonylative coupling to the appropriate phenylboronic acid.

10 lycol) diacrylate) cores functionalized with phenylboronic acid.

11 acryloylated FRET pairs and glucose-specific phenylboronic acid.

12 of heteroaryl chlorides with piperidine and phenylboronic acid.

13 with electron-rich as well as electron-poor phenylboronic acids.

14 thetic sulfonyl- and sulfonamide-substituted phenylboronic acids.

15 role they play in carbohydrate sensing using phenylboronic acids.

16 reversible reaction between the diol TTX and phenylboronic acids.

17 o-(Pyrrolidinylmethyl)phenylboronic acid (4) and its complexes with bifunction

18 e in vivo use of the peroxynitrite scavenger phenylboronic acid, a novel synthetic molecule having hi

19 The complexation of the phenylboronic acid and cis-diol groups of glucose enable

20 employing dynamic covalent chemistry between phenylboronic acid and cis-diol modified poly(ethylene g

21 eblon, MDM2, VHL, and BRD with complementary phenylboronic acid and diol/catechol linkers, we have su

22 a range of aryl halides (X = Cl, Br, I) with phenylboronic acid and in the reduction of 4-nitrophenol

23 work, we studied the Suzuki reaction between phenylboronic acid and iodobenzene catalyzed by PVP-Pd n

24 At physiological pH, phenylboronic acid and its boronate esters are oxidized

25 In this work, the reaction between phenylboronic acid and the diol-containing, fluorescent

26 ity toward oxidation than more commonly used phenylboronic acids and benzoxaboroles.

27 Case studies of oxidative hydroxylation of phenylboronic acids and dimerization of thiophenol demon

28 n of association constants for commonly used phenylboronic acids and diols in different solvents.

29 ally for a series of meta-, para-substituted phenylboronic acids and diols of variable acidity.

30 ium between the organosilicon derivatives of phenylboronic acids and their cyclic six-membered boroxi

31 ponsive moieties, including glucose oxidase, phenylboronic acid, and glucose-binding molecules are ex

32 kHz, while the resonance of the tetrahedral phenylboronic acid anion appears at approximately 600 kH

33 is formed when meta- and/or para-substituted phenylboronic acids are functionalized with a substituen

34 Protocols employing phenylboronic acid as a phase-transfer reagent for Fisch

35 ve, and NaBPh(4) can be used in the place of phenylboronic acid as a phenylating agent.

36 We make use of phenylboronic acid as a receptor for saccharide capture

37 scheme exploited a diol sensor (meta-fluoro-phenylboronic acid at Gly(A1)) and internal diol (3,4-di

38 ve, long-term nature of both RF read-out and phenylboronic acid-based hydrogels will enable biosensor

39 A phenylboronic acid-based, hydrogel-interlayer Radio-Freq

40 rticoid dexamethasone (Dex) through 1,3-diol/phenylboronic acid chemistry and hydrophobic interaction

41 We show that the bis-2-(N-methylaminomethyl)phenylboronic acid-decorated N,N'-diphenyl-dihydrodibenz

42 (5F3CPBA), and 3-carboxy-5-nitro- (5N3CPBA) phenylboronic acids, demonstrating a clear link between

43 surface functionalization using a thiolated phenylboronic acid derivative, gold-coated piezoresistiv

44 cies corresponding to pKa differences in the phenylboronic acid derivatives directly connect the mole

45 tworks formed from mixtures of two different phenylboronic acid derivatives with unique diol complexa

46 rolled by the relative concentrations of the phenylboronic acid derivatives.

47 many mono- and disaccharides using in-source phenylboronic acid derivatization, resulting in parts-pe

48 igosaccharides using in-source droplet-based phenylboronic acid derivatization.

49 orophenylboronic acid via glucose-responsive phenylboronic acid-diol complexation and electrostatic a

50 ned by introducing a boronate ester linkage (phenylboronic acid-dopamine interaction) and polydopamin

51 itate hydrophobic interactions, as well as a phenylboronic acid for glucose sensing.

52 noelectrode design involves the use of amino phenylboronic acid for the oriented immobilization of an

53 acrylamide-15-crown-5 hydrogel, with pendent phenylboronic acid groups.

54 nyl)porphyrin] or a peroxynitrite scavenger (phenylboronic acid) had markedly less Tlr4 recruitment i

55 with the boronic (neutral, trigonal) form of phenylboronic acid; however, the boronate (anionic, tetr

56 cally tuned hydrogel network, composed of HA-phenylboronic acid (HP) and HA-dopamine (HD), was design

57 Phenylboronic acid-hydrogels exhibit volumetric and diel

58 rates containing basic nitrogen centers with phenylboronic acid in the absence of added base and liga

59 onstants of AcO(-) with 3- and 4-substituted phenylboronic acids in DMSO is nonlinear, with a small n

60 The use of siloxane derivatives of phenylboronic acids in Suzuki-Miyaura and Chan-Lam cross

61 The addition of phenylboronic acid is found to lead to the stability of

62 Polyvalent phenylboronic acid-labeled bovine serum albumin (BSA@PBA

63 We have synthesized a PEGylated, phenylboronic acid modified L-DOPA pro-antioxidant (pPAD

64 oenvironment (TME)-adapted hydrogel with the phenylboronic acid-modified dipyridamole prodrug (DIPP)

65 exposed to high glucose concentrations, the phenylboronic acid moieties of the polymers bind rapidly

66 he final synthetic step, installation of the phenylboronic acid moieties.

67 ); 3-carboxy- (3CPBA) and 4-carboxy- (4CPBA) phenylboronic acids; N-(4-phenylboronic)succinamic acid

68 by new in-situ developed SELEX method using phenylboronic acid on microtitre plate.

69 the pyran ring, which is either catalyzed by phenylboronic acid or promoted by a Lewis acid.

70 alently linked to three different isomers of phenylboronic acid (ortho, 2; meta, 3; and para, 4) as c

71 Phenylboronic acid (PBA) binds to both ARS and HbA1c via

72 isosteric replacement approach to synthesize phenylboronic acid (PBA) derivatives targeting KPC-2.

73 Both 1-butaneboronic acid (BuBA) and phenylboronic acid (PBA) function as potent competitive

74 afe formulation, we have introduced multiple phenylboronic acid (PBA) moieties onto a linear dendriti

75 Compared to phenylboronic acid (PBA), 1 is a stronger Lewis acid and

76 lMA) nanoparticles (NPs) functionalized with phenylboronic acid (PBA), named GelMAP, for the sustaine

77 depends on calcium and is instead induced by phenylboronic acid (PBA).

78 However, the majority of such work has used phenylboronic acids (PBAs) that suffer from low-affinity

79 are esterified with various para-substituted phenylboronic acids [R(2)-C(6)H(4)-B(OH)(2); R(2) = -OCH

80 chlorides, for example, 4-chlorotoluene and phenylboronic acid reacted at only 60 degrees C in dioxa

81 rophenylcarbamoyl)pyridin-2-ylsulfanylmethyl]phenylboronic acid (SX-517), a potent noncompetitive bor

82 s (the material contains motifs derived from phenylboronic acid to interact with 1,2-diols).

83 Using a series of substituted phenylboronic acids to replace the coumarin lactone of 2

84 emiconductors, the compound was reacted with phenylboronic acid under modified Suzuki-Miyaura couplin

85 nate affinity column, containing sulfonamide-phenylboronic acid, under mild chromatographic condition

86 Under hyperglycaemic conditions, phenylboronic acid units within the polymeric matrix rev

87 y diastereoselective dihydroxylation wherein phenylboronic acid was a water surrogate.

88 For example, trigonal boron in neutral phenylboronic acid, which was used as a model compound,