Flexible access to conformationally-locked bicyclic morpholines

Rachael Bogacki, Duncan M. Gill, William J. Kerr, Scott Lamont, John A. Parkinson, Laura C. Paterson

Research output: Contribution to journalArticle

7 Citations (Scopus)


A preparatively accessible route to a series of conformationally-locked bicyclic morpholines has been developed. This flexible approach allows for diversification in order for a small array of lead-like scaffolds to be synthesised from readily available key building blocks.

Original languageEnglish
Pages (from-to)8931-8933
Number of pages3
JournalChemical Communications
Issue number79
Early online date15 Aug 2013
Publication statusPublished - 11 Oct 2013

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    Bogacki, R., Gill, D. M., Kerr, W. J., Lamont, S., Parkinson, J. A., & Paterson, L. C. (2013). Flexible access to conformationally-locked bicyclic morpholines. Chemical Communications, 49(79), 8931-8933. https://doi.org/10.1039/c3cc45627g