A versatile total synthesis of α-D-purpurosaminides C
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Studies on Aminosugars. XXXI. Synthesis of 3,4-Dideoxy-3-enosides and the Corresponding 3,4-Dideoxysugars
2. Methode d'acces aux derives diamino-tetradesoxy-hexoses: synthese de la purpurosamine c, composant de l'antibiotique gentamycine c1a
3. Syntheses of derivatives of 2,6-diamino-2,3,4,6-tetradeoxy-DL-erythro-hexose (DL-purpurosamine C) and 2,6-diamino-2,3,4,6-tetradeoxy-DL-threo-hexose (epi-DL-purpurosamine C)
4. Syntheses of derivatives of 2,6-diamino-2,3,4,6-tetradeoxy-D-erythro-hexose (purpurosamine C), a component of gentamycin C1a
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1. Enantiopure purpurosamine C type glycosyl donors an improved access from rac-acrolein dimer — biocatalytic resolution;Tetrahedron Letters;1997-04
2. Biocatalytic resolutions in total syntheses of purpurosamine and sannamine/sporamine type building blocks of aminoglycoside antibiotics;Tetrahedron Letters;1995-07
3. Sannamycin-type aminoglycoside antibiotics of natural and non-natural (mirror-image) configuration — total syntheses and biological activity;Liebigs Annalen;1995-02
4. Aminoglycoside Antibiotics — Modified, Enantiopure Sannamine‐ and Sporamine‐Type Glycosyl Acceptors;Chemische Berichte;1994-09
5. Total syntheses of enantiomerically pure D- and L-glycosyl donors as components of sannamycin-type aminoglycoside antibiotics;Journal of the Chemical Society, Perkin Transactions 1;1994
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