Oxidation of N,N-Disubstituted Hydroxylamines to Nitrones: The Search for More Sustainable Selective and Practical Stoichiometric Oxidants
Authors: Matassini C., Cardona F.
Autors Affiliation: Univ Florence, Dipartimento Chim, Via Lastruccia 3-13, I-50019 Sesto Fiorentino, FI, Italy; CNR INO, Via N Carrara 1, Sesto Fiorentino, FI, Italy
Abstract: Nitrones are key intermediates for the total synthesis of nitrogen-containing natural products and analogues. The direct oxidation of the corresponding N,N-disubstituted hydroxylamines is one of the most straightforward methods to access such compounds. In this account, we describe the state of the art of this oxidative transformation using stoichiometric reagents. We will focus on the efforts made in the last 25 years to oxidize polyhydroxylated cyclic hydroxylamines, due to our long-standing interest in the total synthesis of alkaloids and other glycomimetics. Particular attention will be devoted to the discussion of the regioselectivity issue arising when unsymmetrical and highly functionalized substrates are involved
Volume: 71 (9) Pages from: 558 to: 561
KeyWords: N,N-Disubstituted hydroxylamines; Nitrones; Oxidation; Regioselectivity; Stoichiometric reagentsDOI: 10.2533/chimia.2017.558Citations: 7data from “WEB OF SCIENCE” (of Thomson Reuters) are update at: 2021-10-24References taken from IsiWeb of Knowledge: (subscribers only)Connecting to view paper tab on IsiWeb: Click hereConnecting to view citations from IsiWeb: Click here