Spiropentane Mimics of Nucleosides: Analogues of 2‘-Deoxyadenosine and 2‘-Deoxyguanosine. Synthesis of All Stereoisomers, Isomeric Assignment, and Biological Activity-Reference-Cited by-同舟云学术

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

Published:2000-02-08 Issue:5 Volume:65 Page:1280-1290
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Guan Hui-Ping¹,Ksebati Mohamad B.¹,Cheng Yung-Chi¹,Drach John C.¹,Kern Earl R.¹,Zemlicka Jiri¹

Affiliation:

1. Department of Chemistry, Experimental and Clinical Chemotherapy Program, Barbara Ann Karmanos Cancer Institute, Wayne State University School of Medicine, 110 East Warren Avenue, Detroit, Michigan 48201-1379, Central Instrumentation Facility, Department of Chemistry, Wayne State University, Detroit, Michigan 48202, Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06510-8066, Department of Biologic and Materials Sciences, School of Dentistry, University of Michigan,...

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo991030r

Reference33 articles.

1. Nucleic acid derived allenols. Unusual analogs of nucleosides with antiretroviral activity

2. Zemlicka, J. In ref 1, pp 73−100.

3. Antiviral Nucleoside Analogues with Axial Chirality

4. Inhibition of replication of hepatitis B virus by cytallene in vitro

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