Issue 3, 1996
From the journal:

Chemical Communications

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

Sung Ho Kang  and  Do Hyun Ryu  

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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Article information

DOI
https://doi.org/10.1039/CC9960000355
Article type
Paper

Chem. Commun., 1996, 355-356

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

S. H. Kang and D. H. Ryu, Chem. Commun., 1996, 355 DOI: 10.1039/CC9960000355

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