Structure of a neothramycin-2′-deoxyguanosine adduct
✍ Scribed by Ichiro N. Maruyama; Nobuo Tanaka; Shinichi Kondo; Hamao Umezawa
- Book ID
- 118315553
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 322 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0006-291X
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📜 SIMILAR VOLUMES
The SO 4 --oxidation of cyclic 1,N 2 -propano-2%-deoxyguanosine, chemo-and regioselectively produced in the reaction of 2%-deoxyguanosine with excessive acetaldehyde or crotonaldehyde, resulted in the smooth formation of (4-hydroxy-5hydroxymethyltetrahydrofuran-2-ylimino)-(4-hydroxy-6-methyltetrahyd
Several biologically important N 2 -adducts of 2 H -deoxyguanosine (dG) that previously were dicultly accessible, have been synthesized directly by means of the Buchwald±Hartwig reaction. The reaction employed in each case involves the coupling of 2 H -deoxy-2-bromoinosine with the appropriate amine