The cyclopropanation of unsaturated ketones in 'super-basic' media

Article abstract of DOI:10.1080/00397919608002618

A modified cyclopropanation of unsaturated ketones using dimethyloxosulfonium methide in 'super basic' media generates exclusively the trans products in high yields (86-95%).

Full text of DOI:10.1080/00397919608002618

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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The Cyclopropanation of
Unsaturated Ketones in
“
Super-Basic” Media
a b
V. M. Shostakovsky & R. M. Carlson
a
N.D. Zelinsky Institute of Organic Chemistry,
Russian Academy of Sciences , Moscow, RUSSIA
b
Department of Chemistry , University of
Minnesota , Duluth, Minnesota, 55812, USA
Published online: 21 Aug 2006.
To cite this article: V. M. Shostakovsky & R. M. Carlson (1996) The Cyclopropanation
of Unsaturated Ketones in “Super-Basic” Media, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 26:9,
1785-1788, DOI: 10.1080/00397919608002618
To link to this article: http://dx.doi.org/10.1080/00397919608002618
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