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High-resolution inkjet printing of all-polymer transistor circuits.
It is shown that the use of substrate surface energy patterning to direct the flow of water-based conducting polymer inkjet droplets enables high-resolution definition of practical channel lengths of 5 micrometers, and high mobilities were achieved.
Synthesis and mutagenicity of A-ring reduced analogues of 7,12-dimethylbenz[a]anthracene.
The synthesis and mutagenicity of two derivatives of 7,12-dimethylbenz[a]anthracene (DMBA) are reported, and both reduced analogues exhibited mutagenic activity in the Ames assay in the presence or absence of microsomal activation for strains TA98 and TA100.
Adrenal medulla imaging agents: a structure-distribution relationship study of radiolabeled aralkylguanidines.
Preliminary evidence suggests that 125I-labeled aralkylguanidines 2b is a storage analogue of norepinephrine, and is now being used clinically in imaging and radiotherapy of catecholamine tumors, such as pheochromocytoma.
A novel and efficient synthesis of fluoromethyl phenyl sulphone and its use as a fluoromethyl Wittig equivalent
A new synthesis of fluoromethyl phenyl sulphone (2) and the reaction conjugate base (3) with carbonyl compounds provides β-fluoro-alcohols (5), which are utilized to prepare terminal vinyl fluorides
A novel polycarbonate for high temperature electro-optics via azo bisphenol amines accessed by Ullmann coupling
Ullmann coupling of benzyl ether protected 4-iodophenol with 4-nitrophenylazo aniline followed by deprotection in trifluoroacetic acid affords novel
Development of a kit-form analog of metaiodobenzylguanidine.
A AIBG shows an affinity for the heart and adrenal medullae of dog and monkey similar to that of MIBG and shows improved selectivity for the adrenergic nerves of the heart as demonstrated by chemical sympathectomy studies.
Benzisoxazolo[2,3-a]pyridinium tetrafluoroborates. Possible generation of an aryloxenium ion
Thermolysis and photolysis of the title compounds (1) give aryloxenium ions which undergo intermolecular reactions when R = H but intramolecular cyclisation when R = NO2.