One-step conversion of oximes to gem-chloro-nitro derivatives
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Electron transfer processes. 37. Free radical chain nucleophilic substitution reactions of 1-chloro-1-cyclopropyl-1-nitroethane and 2-chloro-2-nitrohept-6-ene
2. A novel stereochemical control
3. Bromonitromethane—a versatile electrophile
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1. Reaction of Aldoximes with Sodium Chloride and Oxone under Ball-Milling Conditions;Molecules;2020-08-14
2. Oxidation of 3β-Acetoxy-21β-acetyl-20β,28-epoxy-18α,19βH-ursane into Novel gem-Chloronitro- and 1,2,4,5-tetraoxane derivatives;Natural Product Communications;2018-03
3. Synthesis of triterpenoid-based ring-A azepanone and gem-3-nitro-3-chloro- derivatives by ozonolysis of 3-oximino-28-oxoallobetulin under normal and acidic solvolysis conditions;Tetrahedron;2017-07
4. Recent Developments in the Chemistry ofgem-Halonitro Compounds;European Journal of Organic Chemistry;2014-07-17
5. Journey Describing Applications of Oxone in Synthetic Chemistry;Chemical Reviews;2013-03-01
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