Facilitation of displacements at the 6-position of purines by the use of 1,4-diazabicyclo[2.2.2]octane as leaving group. [Erratum to document cited in CA126:251122]

Nicola K Lembicz, Sharon Grant, William Clegg, Roger J Griffin, Sarah L Heath, Bernard T Golding

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The ability of 1,4-diazabicyclo[2.2.2]octane (DABCO) to catalyze reactions of 2-amino-9-benzyl-6-chloro-9H-purine with alkoxides has been demonstrated (J. A. Linn, E. W. McLean and J. L. Kelley, J. Chem. Soc., Chem. Commun., 1994, 913). These authors also characterized 1-1-(2-amino-9-benzyl-9H-purin-6-yl)-4-aza-1-azoniabicyclo[2.2.2]octane chloride from reaction of DABCO with 2-amino-9-benzyl-6-chloro-9H-purine in DMF. DABCO has been shown to catalyze reactions or 6-chloropurines with cyanide (M. Hocek and A. Holy, Collect. Czech. Chem. Commun., 1995, 60, 1386). [on SciFinder(R)]
    Original languageEnglish
    JournalJ. Chem. Soc., Perkin Trans. 1
    Issue number23
    Publication statusPublished - 1997

    Keywords

    • erratum purine diazabicyclooctane prepn substitution
    • purine diazabicyclooctane prepn substitution erratum
    • alkoxypurine prepn erratum

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