Electrophilic cyclization of allylic 1,1-dimethylisoureas with N-iodosuccinimide and phenylselenenyl triflate

Article abstract of DOI:10.1080/00397919508012678

New procedures are described for the cyclization of allylic 1,1-dimethylisoureas. Efficient cyclization of the isoureas to give substituted oxazolines occurs with both N-iodosuccinimide and phenylselenenyl triflate. Reductive dehalogenation can be carried

Full text of DOI:10.1080/00397919508012678

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Electrophilic Cyclization of
Allylic 1,1- Dimethylisoureas
with N-Iodosuccinimide and
Phenylselenenyl Triflate
Robert M. Giuliano a & Carol Bigos a
a Department of Chemistry , Villanova University ,
Villanova, PA, 19085
Published online: 23 Sep 2006.
To cite this article: Robert M. Giuliano & Carol Bigos (1995) Electrophilic Cyclization
of Allylic 1,1- Dimethylisoureas with N-Iodosuccinimide and Phenylselenenyl Triflate,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 25:8, 1145-1153
To link to this article: http://dx.doi.org/10.1080/00397919508012678
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