Synthesis and introduction into DNA of benzo[a]pyrene adducts at the N2-position of deoxyguanosine and the N6-position of deoxyadenosine.

被引：0

作者：

Johnson, F ^{[1
]}

Bonala, RR ^{[1
]}

Tawde, DS ^{[1
]}

Torres, MC ^{[1
]}

机构：

[1] SUNY Stony Brook, Dept Pharmacol, Stony Brook, NY 11794 USA

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2002年 / 224卷

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

076-TOXI

引用

页码：U374 / U374

页数：1

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[1] Synthesis and introduction into DNA of Benzo[a]pyrene adducts at the N2-position of deoxyguanosine and the N6-position of deoxyadenosine
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Bonala, RR
Tawde, DS
Torres, MC
[J]. CHEMICAL RESEARCH IN TOXICOLOGY, 2002, 15 (12) : 1669 - 1670
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[3] Solvent-free synthesis of benzo[a]pyrene 7,8-diol 9,10-epoxide adducts at the N2-position of deoxyguanosine
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[J]. ORGANIC LETTERS, 2001, 3 (04) : 531 - 533
[4] Efficient synthesis of the benzo[a]pyrene metabolic adducts of 2′-deoxyguanosine and 2′-deoxyadenosine and their direct incorporation into DNA
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[5] Synthesis of DNA adducts of deoxyadenosine and deoxyguanosine with cyclopenta[cd]pyrene.
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[7] Synthesis of pyrene and benzo[α]pyrene adducts at the exocyclic amino groups of 2′-deoxyadenosine and 2'-deoxyguanosine by a palladium-mediated C-N bond-formation strategy
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[8] A general method for the synthesis of the N2- and N6- carcinogenic amine adducts of 2′-deoxyguanosine and 2′-deoxyadenosine
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (45) : 10453 - 10460
[9] SYNTHESIS AND RESOLUTION OF PUTATIVE DIASTEREOMERIC N(2)-DEOXYGUANOSINE AND N(6)-DEOXYADENOSINE ADDUCTS OF BIOLOGICALLY-ACTIVE CYCLOPENTAPAH
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