Synthesis of acosamine and daunosamine from sugar σ-enelactones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference25 articles.
1. Synthesis of enantiomerically pure 2,3-disubstituted isoxazolidin-5-ones
2. An approach to carbapenems from α,β-unsaturated sugar lactones
3. Stereocontrolled entry to negamycin from d-glucose
4. Isoxazolidin-5-one - isoxazolidine rearrangement, an entry to 3-amino-3-deoxy sugars
5. The synthesis of methyl 3-amino-2,3,6-trideoxy-α-L-arabino-hexopyranoside, a structural analog of daunosamine
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2. An Efficient Cascade Synthesis of Ethyl 3-Amino-5-oxoisoxazolidine-4-carboxylate Derivatives;Synthesis;2017-07-11
3. A Meldrum's Acid Based Multicomponent Synthesis of N -Fmoc-isoxazolidin-5-ones: Entry to N -Fmoc-β-amino Acids;European Journal of Organic Chemistry;2017-06-14
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