Trifluoromethylsulfenylation of masked carbonyl compounds

Article abstract of DOI:10.1080/00397910008087435

Incorporation of fluorine and fluorine containing groups such as trifluoromethyl and trifluoromethylthio moieties considerably enhances the biopharmacological properties of the parent precursors. Trifluoromethylsulfenylation of masked carbonyl functions,

Full text of DOI:10.1080/00397910008087435

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Synthetic Communications: An
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Organic Chemistry
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Trifluoromethylsulfenylation of
Masked Carbonyl Compounds
a
b
b
S. Munavalli , D. K. Rohrbaugh , D. I. Rossman ,
b
b
b
F. J. Berg , G. W. Wagner & H. D. Durst
a
Geo-Centers, Inc., Gunpowder Branch , P. O. Box
8, Aberdeen Proving Ground, MD, 21010
6
b
U. S. Army , Edgewood Chemical Biological
Center , Aberdeen Proving Ground, MD, 21010
Published online: 04 Dec 2007.
To cite this article: S. Munavalli , D. K. Rohrbaugh , D. I. Rossman , F. J. Berg ,
G. W. Wagner & H. D. Durst (2000) Trifluoromethylsulfenylation of Masked
Carbonyl Compounds, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 30:16, 2847-2854, DOI:
10.1080/00397910008087435
To link to this article: http://dx.doi.org/10.1080/00397910008087435
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