Regioselective synthesis of C-nucleosides by 1,3-dipolar cycloaddition of arylnitrile oxides to 5,6-dideoxy-1,2-O-iso-propylidene-α-d-xylo-hex-5-enofuranose
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
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Cited by 10 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. Stereoselective 1,3-dipolar cycloadditions to heterocyclic compounds;Journal of Heterocyclic Chemistry;2000-05
2. The nitrile oxide/isoxazoline approach to eleven-carbon monosaccharides: cycloaddition of d- and l-arabinonitrile oxides to 5,6-dideoxyhex-5-enofuranoses and characterisation of the resulting 2-isoxazolines;Carbohydrate Research;1999-11
3. 1,3-Dipolar cycloaddition of 1,2-o-isopropylidene-α-d-xylopentadialdo-1,4-furanosenitrile oxide to some alkenes;Journal of Heterocyclic Chemistry;1998-01
4. The Chemistry of C-Nucleosides and Their Analogs I: C-Nucleosides of Hetero Monocyclic Bases;Advances in Heterocyclic Chemistry;1997
5. The nitrile oxide–isoxazoline route to higher-carbon dialdoses;J. Chem. Soc., Chem. Commun.;1994
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