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Issue 34, 2014
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Azabicycles construction: the transannular ring contraction with N-protected nucleophiles

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Abstract

Synthetic strategies are one of the most critical factors for the success of a synthetic campaign, but most importantly they are crucial for the economy and the efficiency of the sequence. Within this perspective, the synthesis of azabicyclic scaffolds, constituents of many bioactive alkaloids, can be tackled using tandem transannular ring contractions-protecting group cleavages. Commonly these reactions feature medium-sized cyclic N-protected amines that carry a potential electrophilic site. Under the correct conditions this site is activated, and the protecting group is fragmented, inducing a transannular reaction. For the first time, we review in detail this strategy's applications, which span from the assembly of small molecules to complex molecular architectures.

Graphical abstract: Azabicycles construction: the transannular ring contraction with N-protected nucleophiles

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Publication details

The article was received on 20 May 2014, accepted on 27 Jun 2014 and first published on 27 Jun 2014


Article type: Review Article
DOI: 10.1039/C4OB01311E
Author version available: Download Author version (PDF)
Citation: Org. Biomol. Chem., 2014,12, 6570-6579
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    Azabicycles construction: the transannular ring contraction with N-protected nucleophiles

    A. Rizzo and S. R. Harutyunyan, Org. Biomol. Chem., 2014, 12, 6570
    DOI: 10.1039/C4OB01311E

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