AI Article Synopsis
- The compound C-aminoalditol HNCH-(CHOBn)-CHOH was synthesized from two basic monosaccharides.
- This synthesis involved a strategic introduction of an azide group followed by several protection and deprotection steps.
- The reactivity of the aminoalditol was evaluated through a reductive amination reaction with a specially protected form of sucrose monoaldehyde.
Article Abstract
The C-aminoalditol HNCH-(CHOBn)-CHOH was prepared from two simple monosaccharide building blocks. The synthesis was realized by a regioselective introduction of the azide group and subsequent protection-deprotection transformations. The chemical reactivity of the aminoalditol was tested in the reductive amination reaction with a selectively protected sucrose monoaldehyde.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669227 | PMC |
| http://dx.doi.org/10.3762/bjoc.13.213 | DOI Listing |
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