Issue 3, 2010

Cyanative alkene–aldehyde coupling: Ni(0)–NHC–Et2AlCN mediated chromanol synthesis with high cis-selectivity at room temperature

Abstract

Described are several classes of Ni(0) mediated cyanative alkenealdehyde coupling reactions, providing 6-membered cores, which complement existing cyclization technology in several respects. Et2AlCN was used as both a cyclization accelerator and CN source. The NHC ligand may have a positive effect in differentiating reductive elimination and syn-β-hydride elimination.

Graphical abstract: Cyanative alkene–aldehyde coupling: Ni(0)–NHC–Et2AlCN mediated chromanol synthesis with high cis-selectivity at room temperature

Supplementary files

Article information

Article type
Communication
Submitted
09 Sep 2009
Accepted
26 Oct 2009
First published
13 Nov 2009

Chem. Commun., 2010,46, 466-468

Cyanative alkenealdehyde coupling: Ni(0)–NHC–Et2AlCN mediated chromanol synthesis with high cis-selectivity at room temperature

C. Ho, Chem. Commun., 2010, 46, 466 DOI: 10.1039/B918626C

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