Correction to "Modular, step-efficient palladium-catalyzed cross-coupling strategy to access C6-heteroaryl 2-aminopurine ribonucleosides"

Buchanan, Helena S. and Pauff, Steven M. and Kosmidis, Tilemachos D. and Taladriz-Sender, Andrea and Rutherford, Olivia I. and Hatit, Marine Z. C. and Fenner, Sabine and Watson, Allan J. B. and Burley, Glenn A. (2017) Correction to "Modular, step-efficient palladium-catalyzed cross-coupling strategy to access C6-heteroaryl 2-aminopurine ribonucleosides". Organic Letters, 19 (14). ISSN 1523-7060

[img]
Preview
 Text (Buchanan-etal-OL-2017-Correction-to-modular-step-efficient-palladium-catalyzed-cross-coupling-strategy)
Buchanan_etal_OL_2017_Correction_to_modular_step_efficient_palladium_catalyzed_cross_coupling_strategy.pdf
Final Published Version
License: Creative Commons Attribution 4.0 logo
Download (227kB)| Preview

    Abstract

    Two Pd-catalyzed methods to access 6-heteroaryl 2-aminopurine ribonucleosides from 6-chloroguanosine are described. First, Pd-132-catalyzed Suzuki-Miyaura cross-coupling using a series of boron substrates and 6-chloroguanosine forms 6-heteroaryl-2-aminopurines in a single step. The versatility of 6-chloroguanosine is further demonstrated using a modified Sonogashira coupling employing potassium iodide as an additive. Finally, the utility of the 6-alkynyl-2-aminopurine ribonucleoside as a dipolarophile in [3 + 2] cycloadditions is presented, affording triazoles and isoxazoles when reacted with azide and isonitrile 1,3-dipoles, respectively.

    Creators(s): Buchanan, Helena S. ORCID logoORCID: https://orcid.org/0000-0001-8710-0511, Pauff, Steven M. ORCID logoORCID: https://orcid.org/0000-0002-7499-3207, Kosmidis, Tilemachos D. ORCID logoORCID: https://orcid.org/0000-0001-6194-6092, Taladriz-Sender, Andrea ORCID logoORCID: https://orcid.org/0000-0002-8274-4761, Rutherford, Olivia I. ORCID logoORCID: https://orcid.org/0000-0003-3517-8186, Hatit, Marine Z. C. ORCID logoORCID: https://orcid.org/0000-0002-5713-6596, Fenner, Sabine, Watson, Allan J. B. and Burley, Glenn A.;
    Item type:Article
    ID code:61590
    Keywords:boron substrates, Sonogashira coupling, Suzuki−Miyaura cross coupling, ribonucleosides, Chemistry, Organic Chemistry
    Subjects:Science > Chemistry
    Department:Faculty of Science > Pure and Applied Chemistry
    Depositing user: Pure Administrator
    Date deposited:16 Aug 2017 14:32
    Last modified:08 Feb 2021 03:40
    Related URLs:
    URI:https://strathprints.strath.ac.uk/id/eprint/61590
    Export data:
    CORE (COnnecting REpositories)