ライフサイエンスコーパス: phenylboronic acid

1 lycol) diacrylate) cores functionalized with phenylboronic acid.

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

3 compounds related to both benzoxaborole and phenylboronic acid.

4 to that previously determined for the simple phenylboronic acid.

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

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

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

8 ki carbonylative coupling to the appropriate phenylboronic acid.

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

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

11 thetic sulfonyl- and sulfonamide-substituted phenylboronic acids.

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

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

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

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

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

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

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

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

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

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

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

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

24 (5F3CPBA), and 3-carboxy-5-nitro- (5N3CPBA) phenylboronic acids, demonstrating a clear link between

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

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

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

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

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

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

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

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

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

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

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

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

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

38 ); 3-carboxy- (3CPBA) and 4-carboxy- (4CPBA) phenylboronic acids; N-(4-phenylboronic)succinamic acid

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

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

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

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

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

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

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

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

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

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

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

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