A sequential direct arylation/Suzuki–Miyaura cross-coupling transformation of unprotected 2′-deoxyadenosine affords a novel class of fluorescent analogues

Thomas E. Storr, Johanna A. Strohmeier, Christoph G. Baumann, Ian J. S. Fairlamb

    Research output: Contribution to journalArticlepeer-review

    33 Citations (Scopus)

    Abstract

    Novel rigid 8-biaryl-2′-deoxyadenosines with tuneable fluorescent properties can be accessed by an efficient sequential catalytic Pd0-coupling approach.
    Original languageEnglish
    Pages (from-to)6470-6472
    Number of pages3
    JournalChemical Communications
    Volume46
    Issue number35
    Early online date17 Aug 2010
    DOIs
    Publication statusPublished - 21 Sept 2010

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