Electrophilic Cyclization of Allylic 1,1- Dimethylisoureas with N-Iodosuccinimide and Phenylselenenyl Triflate: Synthetic Communications: Vol 25, No 8

Synthetic Communications

An International Journal for Rapid Communication of Synthetic Organic Chemistry

Volume 25, 1995 - Issue 8

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Abstract

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 out with lithium aluminum hydride.

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Electrophilic Cyclization of Allylic 1,1- Dimethylisoureas with N-Iodosuccinimide and Phenylselenenyl Triflate

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Electrophilic Cyclization of Allylic 1,1- Dimethylisoureas with N-Iodosuccinimide and Phenylselenenyl Triflate

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