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Novel pseudodisaccharide-type aminocyclitol antibiotic models, built up from D-arabinose, D-ribose, D-glucosamine, L-ristosamine and L-acosamine have been synthesized by the glycosylation of suitably protected (azido)deoxyinosose aglycones derived by the Ferrier carbocyclic ring transformation of carbohydrate precursors. An alternative approach to related pseudodisaccharides, based on the Ferrier carbocyclization of reducing disaccharides, has also been elaborated. This latter method extends the scope of the Ferrier reaction, by demonstrating that acid-labile 2-deoxydisaccharides can also be readily transformed into the corresponding pseudodisaccharides under the slightly acidic conditions of this ring-transformation.
I F Pelyvás, and
M Mádi-Puskás, and
Z G Tóth, and
Z Varga, and
M Hornyák, and
G Batta, and
F Sztaricskai
June 2020,
The Journal of organic chemistry,
I F Pelyvás, and
M Mádi-Puskás, and
Z G Tóth, and
Z Varga, and
M Hornyák, and
G Batta, and
F Sztaricskai
April 1985,
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I F Pelyvás, and
M Mádi-Puskás, and
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F Sztaricskai
September 1977,
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I F Pelyvás, and
M Mádi-Puskás, and
Z G Tóth, and
Z Varga, and
M Hornyák, and
G Batta, and
F Sztaricskai
October 2010,
Expert opinion on therapeutic patents,
I F Pelyvás, and
M Mádi-Puskás, and
Z G Tóth, and
Z Varga, and
M Hornyák, and
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F Sztaricskai
December 1979,
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I F Pelyvás, and
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F Sztaricskai
August 1976,
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I F Pelyvás, and
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Z Varga, and
M Hornyák, and
G Batta, and
F Sztaricskai
October 1979,
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I F Pelyvás, and
M Mádi-Puskás, and
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F Sztaricskai
November 1976,
Antibiotiki,
I F Pelyvás, and
M Mádi-Puskás, and
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Z Varga, and
M Hornyák, and
G Batta, and
F Sztaricskai
November 2000,
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I F Pelyvás, and
M Mádi-Puskás, and
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Z Varga, and
M Hornyák, and
G Batta, and
F Sztaricskai
January 1970,
The Journal of antibiotics,
