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Spiropentane Mimics of Nucleosides: Analogues of 2‘-Deoxyadenosine and 2‘-Deoxyguanosine. Synthesis of All Stereoisomers, Isomeric Assignment, and Biological Activity

✍ Scribed by Guan, Hui-Ping; Ksebati, Mohamad B.; Cheng, Yung-Chi; Drach, John C.; Kern, Earl R.; Zemlicka, Jiri

Book ID
111962163
Publisher
American Chemical Society
Year
2000
Tongue
English
Weight
167 KB
Volume
65
Category
Article
ISSN
0022-3263

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📜 SIMILAR VOLUMES

ChemInform Abstract: Spiropentane Mimics
ChemInform Abstract: Spiropentane Mimics of Nucleosides: Analogues of 2′-Deoxyadenosine and 2′-Deoxyguanosine. Synthesis of All Stereoisomers, Isomeric Assignment, and Biological Activity.
✍ Hui-Ping Guan; Mohamad B. Ksebati; Yung-Chi Cheng; John C. Drach; Earl R. Kern; 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Synthesis and Biological Activity of 2-A
Synthesis and Biological Activity of 2-Aminopurine Methylenecyclopropane Analogues of Nucleosides.
✍ Ruifang Wang; Xinchao Chen; John C. Drach; Earl R. Kern; Jiri Zemlicka 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 130 KB 👁 1 views

Synthesis and Biological Activity of 2-Aminopurine Methylenecyclopropane Analogues of Nucleosides. -Racemic 2-aminopurine methylenecyclopropane analogues such as (V) and (VI), as well as the (S)-enantiomer of compound (V) are synthesized and evaluated for their bioactivity. All the racemic compounds