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Showing 1–5 of 5 results
Advanced filters: Author: Andrew V. Kelleghan Clear advanced filters
  • The strained C6H6 isomer 1,2,3-cyclohexatriene and its derivatives participate in a host of reaction modes which demonstrate their potential for selective chemical transformations and provide an unconventional entryway to complex scaffolds.

    • Andrew V. Kelleghan
    • Ana S. Bulger
    • Neil K. Garg
    Research
    Nature
    Volume: 618, P: 748-754
  • A new synthetic method provides a coveted motif, the bicyclo[2.1.1]hexane scaffold, using the uncommon coupling of two strained diradicaloid fragments: transiently generated cyclic allenes and bicyclo[1.1.0]butanes.

    • Arismel Tena Meza
    • Christina A. Rivera
    • Neil K. Garg
    Research
    Nature
    Volume: 640, P: 683-690
  • Strained cyclic allenes are short-lived intermediates that confine a functional group with a preferred linear geometry, an allene, into a small ring, inducing strain-driven reactivity. Now, 2,3-azacyclic and 2,3-oxacyclic allenes are generated and trapped using cycloaddition reactions, generating complex heterocycles that bear a large fraction of sp3-hybridized atoms.

    • Andrew V. Kelleghan
    • Arismel Tena Meza
    • Neil K. Garg
    Research
    Nature Synthesis
    Volume: 3, P: 329-336
  • Simple methods to incorporate deuterium into organic compounds are highly sought after as deuteration can enable mechanistic studies or improve the metabolic stability of pharmaceuticals. Now, a catalytic hydrogen–deuterium exchange reaction using deuterated water allows convenient access to deuterated aldehyde building blocks.

    • Sarah M. Anthony
    • Andrew V. Kelleghan
    • Neil K. Garg
    News & Views
    Nature Catalysis
    Volume: 2, P: 1058-1059