Abstract
We present a protocol for the facile conversion of linear alkenyl N-alkoxy carbamates into cyclic
bromo carbonates. The reaction is operationally simple, uses widely available, inexpensive reagents, and requires
no rigorous exclusion of air or moisture. A broad range of functional groups is compatible, and the reaction diastereoselectivities range from good to excellent. The reactions are scalable, and the product carbonates can be further transformed.
Supplementary materials
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X-ray structure of Compound 25
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