Published in

Thieme Gruppe, Synlett: Accounts and Rapid Communications in Synthetic Organic Chemistry, 10(2008), p. 1510-1514, 2008

DOI: 10.1055/s-2007-1077795

Links

Tools

Export citation

Search in Google Scholar

Synthesis of 8-Heteroaryl-2′-deoxyguanosine Derivatives

Journal article published in 2008 by María del C. Rivera-Sánchez, Gerard Hobley, José M. Rivera, Vladimir Gubala ORCID, María Del C. Rivera-Sánchez
This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Red circle
Preprint: archiving forbidden
Orange circle
Postprint: archiving restricted
Upload
Red circle
Published version: archiving forbidden
Policy details
Data provided by SHERPA/RoMEO

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.