Routes from both γ- and δ-glucoheptonolactones to spirohydantoins of glucofuranose are described, affording further analogues of hydantocidin. It may be that the glucofuranose isomers are more stable than the glucopyranose forms. © 1995
Glycogen phosphorylase (GP) is currently exploited as a target for inhibition of hepatic glycogenoly...
A practical access to glucose-based and allose-based spirooxazolidinones is reported. The synthetic ...
An α-azidocarboxylate of a tetrahydrofuran derived from L-rhamnose may be used as a divergent interm...
Epimeric spirohydantoins of glucofuranose, analogues of hydantocidin, are readily prepared from gluc...
The synthesis of two epimeric spirohydantoins of glucopyranose provides the first examples of pyrano...
A short synthesis of the spirohydantoin of glucopyranose 1β [a potent and specific inhibitor of glyc...
Spironucleosides are a type of conformationally restricted nucleoside analogs in which the anomeric ...
Epimeric azidoesters containing a glucofuranosyl moiety are readily prepared from glucoheptonolacton...
A glucopyranose spirohydantoin (a pyranose analogue of the potent herbicide, hydantocidin) has been ...
The synthesis of (2R,3R,4S,5R,6S)-3,4,5-trihydroxy-2-hydroxymethyl-7,9-diaza-oxaspiro-[ 4,5]decane-8...
this thesis describes the total synthesis of the carbocyclic analogue of hydantocidin and its 6,1-di...
Ionic brominative oxidation of 2-amino derivatives of protected heptonolactones derived from L-rhamn...
Spirohidantoins represent an pharmacologically important class of heterocycles since many derivative...
We present a short, enantiospecific synthesis of four hydroxylated analogues of pyrenolide D from D-...
Glycogen phosphorylase (GP) is currently exploited as a target for inhibition of hepatic glycogenoly...
Glycogen phosphorylase (GP) is currently exploited as a target for inhibition of hepatic glycogenoly...
A practical access to glucose-based and allose-based spirooxazolidinones is reported. The synthetic ...
An α-azidocarboxylate of a tetrahydrofuran derived from L-rhamnose may be used as a divergent interm...
Epimeric spirohydantoins of glucofuranose, analogues of hydantocidin, are readily prepared from gluc...
The synthesis of two epimeric spirohydantoins of glucopyranose provides the first examples of pyrano...
A short synthesis of the spirohydantoin of glucopyranose 1β [a potent and specific inhibitor of glyc...
Spironucleosides are a type of conformationally restricted nucleoside analogs in which the anomeric ...
Epimeric azidoesters containing a glucofuranosyl moiety are readily prepared from glucoheptonolacton...
A glucopyranose spirohydantoin (a pyranose analogue of the potent herbicide, hydantocidin) has been ...
The synthesis of (2R,3R,4S,5R,6S)-3,4,5-trihydroxy-2-hydroxymethyl-7,9-diaza-oxaspiro-[ 4,5]decane-8...
this thesis describes the total synthesis of the carbocyclic analogue of hydantocidin and its 6,1-di...
Ionic brominative oxidation of 2-amino derivatives of protected heptonolactones derived from L-rhamn...
Spirohidantoins represent an pharmacologically important class of heterocycles since many derivative...
We present a short, enantiospecific synthesis of four hydroxylated analogues of pyrenolide D from D-...
Glycogen phosphorylase (GP) is currently exploited as a target for inhibition of hepatic glycogenoly...
Glycogen phosphorylase (GP) is currently exploited as a target for inhibition of hepatic glycogenoly...
A practical access to glucose-based and allose-based spirooxazolidinones is reported. The synthetic ...
An α-azidocarboxylate of a tetrahydrofuran derived from L-rhamnose may be used as a divergent interm...
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