[3,3]-sigmatropic rearrangement step in the gold-catalyzed cyclization of allyl-(ortho-alkinylphenyl)methyl ethers

The gold-catalyzed conversion of allyl-(ortho-alkynylphenyl)methyl ethers was investigated, and allylated isochromenes were obtained. An optimization of the catalysis conditions with respect to different phosphane and carbene ligands on gold, different counterions, and different solvents was conduct...

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Bibliographic Details
Main Authors: Ackermann, Martin (Author) , Bucher, Janina (Author) , Rappold, Melissa (Author) , Graf, Katharina (Author) , Rominger, Frank (Author) , Hashmi, A. Stephen K. (Author)
Format: Article (Journal)
Language:English
Published: May 31, 2013
In: Chemistry
Year: 2013, Volume: 8, Issue: 8, Pages: 1786-1794
ISSN:1861-471X
DOI:https://doi.org/10.1002/asia.201300324
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/https://doi.org/10.1002/asia.201300324
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/asia.201300324
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Author Notes:Martin Ackermann, Janina Bucher, Melissa Rappold, Katharina Graf, Frank Rominger, and A. Stephen K. Hashmi