Chemo-, regio- and stereospecific addition of adenine and 8-azaadenine to α,β-acetylenic γ-hydroxy nitriles: a short-cut to novel acyclic adenosine analogues-Reference-Cited by-同舟云学术

Chemo-, regio- and stereospecific addition of adenine and 8-azaadenine to α,β-acetylenic γ-hydroxy nitriles: a short-cut to novel acyclic adenosine analogues

Published:2010-02 Issue:9 Volume:66 Page:1699-1705
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Trofimov Boris A.,Mal'kina Anastasiya G.,Nosyreva Valentina V.,Shemyakina Olesya A.,Borisova Angela P.,Larina Lyudmila I.,Kazheva Olga N.,Alexandrov Grigorii G.,Dyachenko Oleg A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference60 articles.

1. Synthesis of new acyclonucleosides comprising unexpected regioisomers in the case of purines

2. An Efficient Synthesis Of Acyclic N7- and N9-Adenine Nucleosides Via Alkylation With Secondary Carbon Electrophiles to Introduce Versatile Functional Groups At the C-1 Position of Acyclic Moiety

3. Synthesis and Anti-HIV Activity of Novel Cyclopentenyl Nucleoside Analogues of 8-Azapurine

4. Acyclic Nucleotide Analogs Derived from 8-Azapurines: Synthesis and Antiviral Activity

5. Synthesis Of 2,2,3-Tris(Hydroxymethyl)Methylenecyclopropane Analogues Of Nucleosides

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