7-substituted 7-deaza-2′-deoxyadenosines and 8-aza-7-deaza-2′-deoxyadenosines:: Fluorescence of DNA-base analogues induced by the 7-alkynyl side chain
7-substituted 7-deaza-2′-deoxyadenosines and 8-aza-7-deaza-2′-deoxyadenosines:: Fluorescence of DNA-base analogues induced by the 7-alkynyl side chain
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DOI:
10.1002/(sici)1522-2675(20000510)83:5
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发表时间:
2000-01-01
影响因子:
1.8
通讯作者:
Deimel, M
中科院分区:
文献类型:
--
作者:
Seela, F;Zulauf, M;Deimel, M
7-Alkynylated 7-deazaadenine (pyrrolo[2.3-d]pyrimidin-4-amine) 2'-deoxyribonucleosides show strong fluorescence which is induced by the 7-alkynyl sids chain ( Table 3). A large Stokes shift with an emission around 400 nm is observed when the compound is irradiated at 280 nm. nle solvent dependence indicates the formation of a charged transition state. The fluorescence appears when the triple bond is in conjugation with the heterocyclic base. Electron-donating substituents at the triple bond increase the fluorescence. Hliile electron-withdrawing residues reduce it. In comparison the 7-alkynylated 8-aza-7-deazaadenine (pyrazolo[3,4-d]pyrimidin-4-amine) 2'-deoxyribunucleosides are rather weakly fluorescent (Table 4). Quantum yields and fluorescence decay rimes are measured. The synthesis of the 7-alkynylated 7-duaLa-'.-dc oxyadenosines and Xa; aza-7-deaza-2'-deoxyadenosines was performed with 7-deaza-2'-deoxy-7- iodoadenosine (6) or 8-aza-7-deaza-2' deoxy-7-iodoadenosine (22) as starting materials and employing the Pd"-catalyzed cross-coupling reaction with the corresponding alkynes (Schemes,1, 4, and 5). Catalytic hydrogenation of the side chain ol. die unsaturated nucleosides 5 and 17 afforded the 7-alkyl derivatives 18 and 19. respectively, which do not show significant fluorescence (Scheme 2).