A convenient synthesis of 5-substituted-7-β-D-arabinofuranosylpyrrolo[2,3-d]pyrimidines structurally related to the antibiotics toyocamycin and sangivamycin-Reference-Cited by-同舟云学术

A convenient synthesis of 5-substituted-7-β-D-arabinofuranosylpyrrolo[2,3-d]pyrimidines structurally related to the antibiotics toyocamycin and sangivamycin

Published:1988-05 Issue:3 Volume:25 Page:1043-1046
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:

Author:

Ramasamy Kandasamy,Robins Roland K.,Revankar Ganapathi R.

Publisher

Wiley

Subject

Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.5570250366/fullpdf

Reference21 articles.

1. Preparation of 9-β-D-Arabinofuranosylguanine (araG)

2. Nucleic acid related compounds. 25. Syntheses of arabino, xylo, and lyxo-anhydro sugar nucleosides from tubercidin ribo-epoxide

3. 4‐Amino‐7‐(β‐ D ‐arabinofuranosyl)pyrrolo[2,3‐ d ]pyrimidin — die Synthese von Ara‐Tubercidin durch Phasentransferkatalyse

4. 2-Amino-7-(.beta.-D-arabinofuranosyl)pyrrolo[2,3-d]pyrimidin-4(3H)-one. Synthesis of ara-7-deazaguanosine via phase-transfer glycosylation

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