Regio- and stereo-selective synthesis of carbohydrate isoxazolidines by 1,3-dipolar cycloaddition of nitrones to 5,6-di-deoxy-1,2- O -isopropylidene-α- d - xylo -hex-5-enofuranose
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference28 articles.
Cited by 15 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. Pediatric Delirium Assessment, Prevention, and Management;Delirium;2020
2. Design, synthesis and biological activity evaluation of regioisomeric spiro-(indoline-isoxazolidines) in the inhibition of TNF-α-induced ICAM-1 expression on human endothelial cells;MedChemComm;2012
3. Microwave-Assisted Stereoselective 1,3-Dipolar Cycloaddition of C,N-Diarylnitrone (i.e., N-(Arylmethylidene)benzenamine N-Oxide) and Bis(arylmethylidene)acetone (=1,5-Diarylpenta-1,4-dien-3-one): NMR and Crystal Analysis of Diastereoisomeric Bis(isoxazoli;Helvetica Chimica Acta;2012-01
4. ChemInform Abstract: Regio- and Stereoselective Synthesis of Carbohydrate Isoxazolidines ( III), (IV) by 1,3-Dipolar Cycloaddition of Nitrones (II) to 5,6- Dideoxy-1,2-O-isopropylidene-α-D-xylo-hex-5-enofuranose (I).;ChemInform;2010-08-21
5. 1,3-Dipolar Cycloadditions in the Synthesis of Carbohydrate Mimics. Part 3: Azides, Diazo Compounds and Other Dipoles;Current Organic Chemistry;2003-05-01
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