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Synlett 2013; 24(15): 1973-1977
DOI: 10.1055/s-0033-1338965
DOI: 10.1055/s-0033-1338965
letter
Facile Synthesis of Novel Glycosyl Oxindoles through 1,3-Dipolar Cycloaddition
Further Information
Publication History
Received: 18 April 2013
Accepted after revision: 27 June 2013
Publication Date:
13 August 2013 (online)
![](https://www.thieme-connect.de/media/synlett/201315/lookinside/thumbnails/10.1055-s-0033-1338965-1.jpg)
Abstract
Synthesis of a series of glycosyl spirooxindoles has been accomplished through an intermolecular 1,3-dipolar cycloaddition reaction of an azomethine ylide generated from glucose with the dipolarophile 4-(E)-3-phenacylidene oxindole.
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References and Notes
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