J phenol

Etzensperger, M., Thoma, S., Petrozzi, S., and Dunn, I. J., Phenol Degradation in a Three-Phase Biofilm Fluidized Sand Bed Reactor, Bioproc. Eng., 4 175... 

Substituent j phenols /ortho anilines yortho Substituent j —phenols y ortho —anilines yortho... 

Gil. Goldberg, D. M., Hoffman, B., Yang, J., and Soleas, G. J., Phenolic constituents, furans, and total antioxidant status of distilled spirits. J. Agric. Food Chem. 47, 3978-3985 (1999). 

Appel, J., Phenolics in ecological interactions the importance of oxidation, J. Chem. Ecol., 19, 1521, 1993. 

P15. Prutz, W. A., Butler, J., and Land, E. J., Phenol coupling initiated by one-electron oxidation of tyrosine units in peptides and histone. Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med. 44, 183-196(1983). 

Copp EP, Keenan J. Phenol nerve and motor point block in spasticity. Rheumatol Phys Med 1972 ll(6) 287-92. 

The effect of rf coordination on the arenes was studied in the context of the phe-nol-ketodiene equilibrium . It was shown that this equilibrium for the free ligands favors heavily the phenol tautomer vide supra) whereas for the complexes [Os(NH3)5-2,3- -arene)] + (arene = phenol 2-, 3-, 4-methylphenol 3,4-dimethylphenol) the corresponding equilibrium constants approach unity (20 °C). The conversion of phenol 67 into the 2,4-cyclohexadien-l-one 68 was kinetically favored over the formation of the 2,5-isomer 69, although the latter is the thermodynamically favored product (equation 26). It was assumed that osmium rehybridizes the C(5) and C(6) atoms to form a metallocy-clopropane. This removes much of the resonance energy and therefore destabilizes the enohc form of the free hgand. The free energies of ketonization (25 °C) for the /j -phenol complex in comparison with free phenol are shown in equations 27 and 28 . 

Tanguy, J. Phenol metabohsm and the hypersensitive reaction in Nicotiana infected with tobacco mosaic virus Physiol. Veg. 9 (1971) 169-187. 

MattUa, P. and HeUstrom, J., Phenolic acids in potatoes, vegetables and some of their products. J. Food Comp. Anal, 20, 152-160, 2007. 

Chantraine, J.-M., Combaut, G., Teste, J. Phenols bromes d lme algue rouge, Halopytis incurvus Acides carboxyliques. Phytochemistry 1973, 12, 1793-1796. 

Finckh, R. E., and Ch. Tamm The Homoisoflavones III. Isolation and Structure of Punctatin, 3,9-Dihydropunctatin, 4 -0-Methyl-3,9-dihydropunctatin, 4 -Demethyl-eucomin, and 4 -Demethyl-5-0-methyl-3,9-dihydroeucomin. Experientia 26,472 (1970). Friend, J. Phenolic Substances and Plant Disease. Recent Adv. Phytochemistry 12,... 

Friend, J., Phenolic substances and plant disease, in Biochemistiy of Plant Phenolics (T. Swain, J. B. Harbome, and C. F. van Sumere, eds.). Recent Advances in Phytochemistry Vol. 12), 557-588, Plenum Press, New York, 1979. 

Electrophilic Aromatic Substitution. Micellar SDS has been used as a reaction medium for the chlorination and bromlnatlon of alkyl phenyl ethers T gjj(j phenol by several halogenatlng agents (eq 1). Compared to reactions in H2O alone, theparar.ortho product ratio increased for pentyl, nonyl, and dodecyl phenyl ether, and decreased for anlsole. Enhanced ortho relative to para substitution was obtained with phenol. In each case the observed regios-electivity derived at least in part from alignment of the substrate at the micelle-H20 interface and resultant differential steiic shielding of the para and ortho positions by the micelle superstructure. 

Khanizadeh S, Tsao R, Rekika D, Yang R, DeEll J. Phenolic composition and antioxidant activity of selected apple genotypes. / Food Agric Environ. 2007 5(1) 61—66. 

Runeberg, j. Phenol Dehydrogenations. VIII. Synthesis of Magnolol. Acta Chem. Scand. 12, 188 (1958). 

Niemann, G. J. Phenolic glucosides from needles of Larix laricina. Phytochemistry... 

Benzil C,uHio<>j ) Phenol ( CjHjO. ) Hrynakowski and Staszewski, 1936... 

Gonzalez et at (2000) Gonzalez, A.G. Le6n, R Sanchez-Pinto, L. Padr6n, J.I. Bermejo, J. Phenolic Compoimds of Dragon s Blood from Dracaena draco Journal of Natural Products 63 (2000) 1297-1299... 

Richardson, S. H., Wertz, W. J., Phenolic Resins for Coatings, in Treatise on Coatings, Vol. 1, Part III, Meyers and Long, eds.. New York, Marcel Dekker, 1972, Chapter 3. 

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