A mechanistic model for the selective oxidation of 1,4-diols to γ-lactols by o-iodoxybenzoic acid
Author:
Funder
National Science Foundation
National Institutes of Health
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference6 articles.
1. A mild oxidizing reagent for alcohols and 1,2-diols: o-Iodoxybenzoic acid (IBX) in DMSO
2. A useful 12-I-5 triacetoxyperiodinane (the Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species
3. Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones
4. A method for the selective oxidation of 1,4-diols to lactols
5. The Mechanisms of Chromic Acid Oxidations.
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