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1 allowing the formation of 1,2-di(heteroaryl)benzene derivatives.
4 of a new family of hexakis(phenylbutadiynyl)benzene derivatives (4a-c), the largest of which is the
6 reaction between 1,3,5-tris(N,N-dialkylamino)benzene derivatives and 2 equiv of p-substituted benzene
7 ixtures of polycyclic aromatic hydrocarbons, benzene derivatives, and aromatic aldehydes and ketones
8 ketones, aromatic hydrocarbons, substituted benzene derivatives, and short-chain carboxylic acids ar
12 ectra at zero magnetic field for a series of benzene derivatives, demonstrating the analytical capabi
13 edominantly alkanes, alkane derivatives, and benzene derivatives, discriminated between patients with
15 over a century, chemical transformations of benzene derivatives have been guided by the high selecti
16 ic compounds (VOCs), principally alkanes and benzene derivatives, have been identified in breath from
18 ed isomerizations (QAI) of substituted Dewar benzene derivatives in polymeric media are reported.
19 ian aromatic hydrocarbon (methyl-substituted benzene derivatives, mostly xylenes) contaminated site w
20 e then results in efficient aromatization to benzene derivatives of a regiochemically defined substit
22 isolate a discrete trimeric species a Dewar benzene derivative that is locked in this form through a
23 eview photochemical reactions of a series of benzene derivatives that to various extents should stem
24 etized from 1,3,5-trihydroxybenzene or other benzene derivatives through dehydration and polymerizati
25 ate) chelating ligand, the arene ranges from benzene derivatives to fused polycyclic hydrocarbons, an
26 fluorinated stationary phase and a series of benzene derivatives to study the effect of one single pe
28 unts of monoterpenes, aliphatic alcohols and benzene derivatives, were released using pectinolytic pr
31 esis of eight 1,3,5- and 1,2,4,5-substituted benzene derivatives with long rigid arms containing 4-py
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