Electrophilic fluorination of a highly functionalized pyrrole

Article abstract of DOI:10.1080/00397919408010180

Bromine-lithium exchange of 3-bromo-1-(triisopropylsilyl) pyrrole 6 followed by treatment with N-fluorobenzenesulfonimide gave the fluoropyrrole 8. Application of this methodology to the highly functionalized pyrrole 1 afforded the fluoropyrrole 4, which was found to be inaccessible by other approaches.

Full text of DOI:10.1080/00397919408010180

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Electrophilic Fluorination of a
Highly Functionalized Pyrrole
Keith D. Barnes a , Yulin Hu a & David A. Hunt a
a American Cyanamid Co., Agricultural Research
Division , P.O. Box 400, Princeton, New Jersey,
08543-0400
Published online: 23 Sep 2006.
To cite this article: Keith D. Barnes , Yulin Hu & David A. Hunt (1994) Electrophilic
Fluorination of a Highly Functionalized Pyrrole, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 24:12,
1749-1755, DOI: 10.1080/00397919408010180
To link to this article: http://dx.doi.org/10.1080/00397919408010180
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