## Abstract magnified image 3‐(2‐Hydroxy‐2‐phenylethyl)‐ and 3‐(2‐hydroxy‐1‐phenylethyl)adenine, DNA adducts derived from styrene, along with their 9‐substituted analogues were prepared by alkylation of 8‐bromoadenine with corresponding allyl‐protected bromohydrins followed by a new deallylation p
Syntheses of 7-(2-Hydroxy-1-phenylethyl)- and 7-(2-Hydroxy-2-phenylethyl)guanine, DNA Adducts Derived from Styrene 7,8-Oxide
✍ Scribed by Jan Novák; Igor Linhart; Hana Dvorˇáková
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 222 KB
- Volume
- 2004
- Category
- Article
- ISSN
- 1434-193X
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✦ Synopsis
Abstract
7‐(2‐Hydroxy‐1‐phenylethyl)‐ and 7‐(2‐hydroxy‐2‐phenylethyl)guanines are important DNA adducts which can be used as markers of exposure to styrene. Two synthetic routes leading to these compounds are presented using allyl‐protected bromohydrins as synthetic equivalents of styrene oxide to alkylate 2‐amino‐6‐chloropurine or 7‐methyl‐10‐oxo‐9,10‐dihydropyrimido[1,2‐a]purine as precursors to guanine. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)
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