ライフサイエンスコーパス: benzene derivative

1 ielded the corresponding silicon-substituted benzene derivative.

2 ntally derived properties of monosubstituted benzene derivatives.

3 allowing the formation of 1,2-di(heteroaryl)benzene derivatives.

4 d), phenylvaleric acids (1.1- to 2-fold) and benzene derivatives (1.5-fold) increased; while benzoic

5 Examination of a series of substituted benzene derivatives (12-14) revealed that the optimal po

6 A benzene derivative, 2-nitro-1,3-dimethylbenzene (2-nitro

7 of a new family of hexakis(phenylbutadiynyl)benzene derivatives (4a-c), the largest of which is the

8 erivative (solute) in a mixed solvent of the benzene derivative and CCl4.

9 reaction between 1,3,5-tris(N,N-dialkylamino)benzene derivatives and 2 equiv of p-substituted benzene

10 ixtures of polycyclic aromatic hydrocarbons, benzene derivatives, and aromatic aldehydes and ketones

11 ketones, aromatic hydrocarbons, substituted benzene derivatives, and short-chain carboxylic acids ar

12 However, (1)L(b) ECD bands of several benzene derivatives are associated with a forbidden char

13 f a number of phenol derivatives and various benzene derivatives are investigated.

14 penylium-functionalized (DAC-functionalized) benzene derivatives as high-potential catholytes for non

15 ts; while MRL and 2xMRL of Mep-Form promoted benzene derivatives (benzyl alcohol, benzaldehyde, and t

16 Not only benzene derivatives but also dihydroxynaphthalenes are r

17 We have prepared novel highly functionalized benzene derivatives by regioselective metalation of este

18 ectra at zero magnetic field for a series of benzene derivatives, demonstrating the analytical capabi

19 edominantly alkanes, alkane derivatives, and benzene derivatives, discriminated between patients with

20 The significant amounts of benzene derivatives from the direct bond dissociation of

21 system for the dearomative hydroarylation of benzene derivatives has been developed.

22 over a century, chemical transformations of benzene derivatives have been guided by the high selecti

23 ic compounds (VOCs), principally alkanes and benzene derivatives, have been identified in breath from

24 Benzene derivatives having pK(a) approx. less than 31 ca

25 cobalt-catalysis led to 1,2,3-trisubstituted benzene derivatives in good yields.

26 meters, concentration, and other halogenated benzene derivatives in methanol solution.

27 ed isomerizations (QAI) of substituted Dewar benzene derivatives in polymeric media are reported.

28 ups, the reaction can be applied to numerous benzene derivatives, making it a reliable strategy for a

29 erized by measuring the Raman spectra of the benzene derivative mixtures consisting of benzene, aniso

30 ian aromatic hydrocarbon (methyl-substituted benzene derivatives, mostly xylenes) contaminated site w

31 e then results in efficient aromatization to benzene derivatives of a regiochemically defined substit

32 entified across 27 chemical families, mainly benzene derivatives, organooxygen compounds, fatty acids

33 a pathway to produce valuable cyclohexane or benzene derivatives, presenting enticing opportunities f

34 solutions consisting of mixtures of aromatic benzene derivatives solvated in methanol.

35 ilizes alk(en)ylresorcinols among a panel of benzene-derivative substrates tested.

36 isolate a discrete trimeric species a Dewar benzene derivative that is locked in this form through a

37 eview photochemical reactions of a series of benzene derivatives that to various extents should stem

38 etized from 1,3,5-trihydroxybenzene or other benzene derivatives through dehydration and polymerizati

39 ate) chelating ligand, the arene ranges from benzene derivatives to fused polycyclic hydrocarbons, an

40 fluorinated stationary phase and a series of benzene derivatives to study the effect of one single pe

41 und in benzoate derivatives and by extension benzene derivatives via a molecular sculpting approach.

42 beta forms of 2-amino-2-deoxy-l-idopyranosyl benzene derivatives was accomplished through stereospeci

43 A series of substituted benzene derivatives were evaluated for their ability to

44 unts of monoterpenes, aliphatic alcohols and benzene derivatives, were released using pectinolytic pr

45 Permeation studies using benzene derivatives whose kinetic diameters differ by le

46 ation potentials (in CH(3)CN) of various DAC-benzene derivatives will range from +0.96 to +1.64 V vs

47 Synthesized bis(styryl)benzene derivatives with donor-pi-donor, donor-acceptor-

48 esis of eight 1,3,5- and 1,2,4,5-substituted benzene derivatives with long rigid arms containing 4-py