Preparation of a methyl 3,4-dideoxy-3-C-nitro-α-d-threo-hex-3-enopyranoside bearing a peroxy function at C-2 and its reactions with some nucleophiles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference16 articles.
1. 2?-Nitro-2?-propen-1?-yl 2,2-Dimethylpropanoate (NPP), A Multiple Coupling Reagent
2. Alkaline Epoxidation of Carbohydrate Nitroolefins
3. Preparation, and nucleophilic addition-reactions, of 1,5- anhydro-4,6-O-benzylidene-2,3-dideoxy-2-nitro-d-erythro-hex-2-enitol
4. First preparation of pyranosid nitroolefin having a peroxy group and its reaction with some nucleophiles
5. Reactions of nitro sugars. VII. A study on acetylation and some chemical properties of acetates
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Synthesis of Deoxyglycosides by Desulfurization under UV Light;The Journal of Organic Chemistry;2017-06-16
2. ChemInform Abstract: Preparation of a Methyl 3,4-Dideoxy-3-C-nitro-α-D-threo-hex-3- enopyranoside Bearing a Peroxy Function at C-2 and Its Reactions with Some Nucleophiles.;ChemInform;2010-08-17
3. Preparation of methyl 4,6-di-O-acetyl-3-C-nitro-2-enopyranoside derivatives and their reduction with sodium borodeuteride;Carbohydrate Research;1996-02
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