![(1S) -1- [(2S, 3R) - 3-Hydroxy-2- azetidinyl] -1, 2- ethanediol](https://static.cymitquimica.com/products/3D/img/MH163530.png "Click to enlarge")
(1S) -1- [(2S, 3R) - 3-Hydroxy-2- azetidinyl] -1, 2- ethanediol
Ref. 3D-MH163530
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Product Information
Glycosylation of azetidinol is a chemical reaction in which a glycosylate group is transferred from an activated sugar to the nitrogen atom of an azetidinone. It can be used for the synthesis of oligosaccharides and polysaccharides by transferring the glycosyl group to their nitrogen atoms. Click modification refers to a type of chemical reaction that was developed by K. Barry Sharpless in 1996, which uses copper-catalyzed azide-alkyne cycloaddition. This type of reaction has been used for the synthesis of complex carbohydrates with high purity and low cost, as well as for modifying sugars with methyl groups or fluorine atoms.
Chemical properties
Technical inquiry about: 3D-MH163530 (1S) -1- [(2S, 3R) - 3-Hydroxy-2- azetidinyl] -1, 2- ethanediol
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