Double asymmetric iodoamination; synthesis of C2 symmetric and meso-amino alcohols

Chemical Communications Pub Date: 1900-01-01 DOI: 10.1039/CC9960000355

Abstract

Alkenic diols 2 and 14 are iodocyclized providing dihydro-1,3-oxazine 3 and dihydrooxazole 15 in 90 and 93% de, respectively, which are precursors of various C2 symmetric and meso-amino alcohols.

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