Home > Research > Publications & Outputs > Palladium-catalyzed construction of quaternary ...

Electronic data

  • Accepted Manuscript

    Rights statement: This is the author’s version of a work that was accepted for publication in Tetrahedron Letters. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Tetrahedron Letters, 57, 32, 2016 DOI: 10.1016/j.tetlet.2016.06.131

    Accepted author manuscript, 1.14 MB, PDF document

    Available under license: CC BY-NC-ND: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License

Links

Text available via DOI:

View graph of relations

Palladium-catalyzed construction of quaternary carbon centers with propargylic electrophiles

Research output: Contribution to journalJournal article

Published
<mark>Journal publication date</mark>10/08/2016
<mark>Journal</mark>Tetrahedron Letters
Issue number32
Volume57
Number of pages10
Pages (from-to)3586-3595
Publication StatusPublished
Early online date1/07/16
<mark>Original language</mark>English

Abstract

This short review describes the broad reactivity of propargylic electrophiles with nucleophiles under palladium catalysis for the construction of quaternary carbon centers, leading to allenylation, propargylation, and alkenylation/allylic alkylation. Although the allenylation and propargylation of a nucleophile can readily create congested carbon centers, these processes often compete and require careful tuning of substrate structure and reactivity of the nucleophile. The alkenylation/allylic alkylation sequence is a much more studied reactivity mode, which results in the coupling of two nucleophiles. This approach is very popular for the rapid generation of molecular complexity, but also poses several chemo- and regioselectivity issues. These selectivity problems have been traditionally overcome by tethering strategies and cyclization reactions. However, over the past few years, highly selective intermolecular coupling reactions of nucleophiles have also been developed. It is, therefore, unsurprising that, as our prowess to control selectivity has grown, the first methods for the palladium-catalyzed enantioselective installation of quaternary carbon centers with propargylic electrophiles have also appeared.

Bibliographic note

This is the author’s version of a work that was accepted for publication in Tetrahedron Letters. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Tetrahedron Letters, 57, 32, 2016 DOI: 10.1016/j.tetlet.2016.06.131