Peracid induced ring opening of some isoxazolidines and oxidation of saturated 1,3-oxazines to new heterocyclic nitrones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Nitrone cycloaddition: peroxy acid oxidation of 2-phenyl-1-oxa-9-azabicyclo[4.3.0]nonane
2. Peracid induced ring opening of isoxazolidines. A mechanistic study.
3. Peracid oxidation of 1-oxa-8-azabicyclo [3,3,0] octanes: An entry to the cis-2,5-disubstituted pyrrolidines.
4. Cycloaddition of 5-substituted 1- pyrroline 1-oxide and conversion of the nitrone cycloadducts into cis-and trans- 2,5-disubstituted pyrrolidines
5. Nitrone cycloaddition : peracid oxidation of perhydro-1,2-oxazolo[3,2-c][1,4]oxazines
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1. The optical nonlinear properties of a new synthesized azo-nitrone compound;Optical Materials;2021-03
2. Isoxazolidine: A Privileged Scaffold for Organic and Medicinal Chemistry;Chemical Reviews;2016-12-16
3. 2,8-Diheterobicyclo[3.2.1]octane Ring Systems: Natural Occurrence, Synthesis and Properties;Synlett;2014-05-08
4. From isoxazolidines to tetrahydro-1,3-oxazines for the synthesis of chiral pyrrolidines;RSC Advances;2012
5. ChemInform Abstract: Peracid-Induced Ring Opening of Some Isoxazolidines and Oxidation of Saturated 1,3-Oxazines to New Heterocyclic Nitrones.;ChemInform;2010-06-17
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