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Metabolites of polycyclic aromatic hydrocarbons. II. Isomeric k-region phenols and methyl ethers of benz [a]anthracene

โœ Scribed by J.C. Wiley Jr.; C.S. Menon; D.L. Fischer; J.F. Engel


Book ID
104214910
Publisher
Elsevier Science
Year
1975
Tongue
French
Weight
196 KB
Volume
16
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


Polycyclic aromatic hydrocarbons (PAR) are metabolized primarily by enzymatic oxyganation which converts the hydrocarbons into polycyclic phenols, dihydrodiols, quinones, etc., and water-soluble conjugates.

1 These metabolites are thought to be formed via eporfde intermedi-2 ates, which readily isomerise to phenols. Metabolic studies of carcinogenic PAR require the availability of authentic samples of these metabolites, thus we have recently re-eramined the syntheses of some PAD K-region phenols via acid-catalyzed dehydration of their parent cis-dihydrodiols.


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โœ Kenneth C. Kolwyck; W. P. Duncan; James F. Engel; James K. Selkirk ๐Ÿ“‚ Article ๐Ÿ“… 1976 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 223 KB

Recent i n v e s t i g a t i o n s concerning t h e o x i d a t i v e metabolism of b e n z o k lpyrene (Be) have implicated various epoxides as intermediates [l].