A lithiation route to c-5 substitution of an imidazole nucleoside and its application to the synthesis of 3-deazaguanosine-Reference-Cited by-同舟云学术

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A lithiation route to c-5 substitution of an imidazole nucleoside and its application to the synthesis of 3-deazaguanosine

Published:1986-01 Issue:7 Volume:42 Page:1971-1980
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Tanaka Hiromichi,Hirayama Masashi,Suzuki Masahiro,Miyasaka Tadashi,Matsuda Akira,Ueda Tohru

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference32 articles.

1. Imidazole Nucleosides and Nucleotides

2. Synthesis and antiviral and antimicrobial activity of certain 1-.beta.-D-ribofuranosyl-4,5-disubstituted imidazoles

3. Fluoroimidazoles as antiviral agents and inhibitors of polynucleotide biosynthesis

4. Synthesis and antiviral evaluation of nucleosides of 5-methylimidazole-4-carboxamide

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1. Lithiation and Alkylation of the Imidazole Backbone;European Journal of Organic Chemistry;2023-05-04

2. Chemical Structure-Biological Activity Models for Pharmacophores’ 3D-Interactions;International Journal of Molecular Sciences;2016-07-08

3. 6-(Arylmethyl)pyrimidin-4(3H)-ones: anthology and prospects of highly efficient anti-HIV agents;Russian Chemical Bulletin;2012-07

4. Synthesis and hybridization properties of oligodeoxynucleotides incorporating 2-N-carbamoylguanine derivatives as guanine analogs;Tetrahedron Letters;2007-07

5. Design of Anti-HIV Ligands by Means of Minimal Topological Difference (MTD) Method;International Journal of Molecular Sciences;2006-11-29

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