Nucleosides 137. Synthetic Modifications at the 2′Position of Pyrrolo[3,2-D]Pyrimidine and Thieno[3,2-D]Pyrimidine C-Nucleosides, Synthesis of “2′-Deoxy-9-Deazzadenosine” and of “9-Deaza ARA-A”-Reference-Cited by-同舟云学术

Nucleosides 137. Synthetic Modifications at the 2′Position of Pyrrolo[3,2-D]Pyrimidine and Thieno[3,2-D]Pyrimidine C-Nucleosides, Synthesis of “2′-Deoxy-9-Deazzadenosine” and of “9-Deaza ARA-A”

Published:1986-12 Issue:5 Volume:5 Page:539-569
ISSN:0732-8311
Container-title:Nucleosides and Nucleotides
language:en
Short-container-title:Nucleosides and Nucleotides

Author:

Rao Kambhampati V. B.,Ren Wa-Yun,Burchenal Joseph H.,Klein Robert S.

Publisher

Informa UK Limited

Subject

Genetics,Biochemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/07328318608068696

Reference28 articles.

1. Presented in part at the 189th National Meeting of the American Chemical Society. April, May28, 31985, Miami Beach, FL. Miami Beach, FL: American Chemical Society. see Abstracts of Papers CARB. 39.

2. Synthesis of the pyrrolo[3,2-d]pyrimidine C-nucleoside isostere of inosine

3. Synthesis of “9-deazaadenosine”; A new cytotoxic C-nucleoside isostere of adenosine

4. Synthesis of "9-deazaguanosine" and other new pyrrolo[3,2-d]pyrimidine C-nucleosides

5. Synthetic studies of the thieno[3,2-d]pyrimidine C-nucleoside isostere of inosine

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