Literature DB >> 20428320

Synthesis of 8-Heteroaryl-2'-deoxyguanosine Derivatives.

Gerard Hobley1, Vladimir Gubala, María Del C Rivera-Sánchez, José M Rivera.   

Abstract

We describe the synthesis of 8-heteroaromatic-2'-deoxyguanosine analogues using Suzuki-Miyaura or Stille conditions. Unprotected and protected 8-bromo-2'-deoxyguanosine was coupled with commercially available heteroarylboronic acids or the trialkyltin derivatives of 2-pyridylbromides either with or without microwave irradiation in good yields.

Entities:  

Year:  2008        PMID: 20428320      PMCID: PMC2860324          DOI: 10.1055/s-2007-1077795

Source DB:  PubMed          Journal:  Synlett        ISSN: 0936-5214            Impact factor:   2.454


  23 in total

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9.  Preparation of C8-amine and acetylamine adducts of 2'-deoxyguanosine suitably protected for DNA synthesis.

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1.  Probing the Limits of Supramolecular G-Quadruplexes Using Atomistic Molecular Dynamics Simulations.

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3.  Walking a supramolecular tightrope: a self-assembled dodecamer from an 8-aryl-2'-deoxyguanosine derivative.

Authors:  María del C Rivera-Sánchez; Ivonne Andújar-de-Sanctis; Marilyn García-Arriaga; Vladimir Gubala; Gerard Hobley; José M Rivera
Journal:  J Am Chem Soc       Date:  2009-08-05       Impact factor: 15.419

4.  Isostructural self-assembly of 2'-deoxyguanosine derivatives in aqueous and organic media.

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